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Logo of bmcebBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Evolutionary Biology
BMC Evol Biol. 2010; 10: 210.
Published online Jul 13, 2010. doi:  10.1186/1471-2148-10-210
PMCID: PMC3017758

BMGE (Block Mapping and Gathering with Entropy): a new software for selection of phylogenetic informative regions from multiple sequence alignments

Abstract

Background

The quality of multiple sequence alignments plays an important role in the accuracy of phylogenetic inference. It has been shown that removing ambiguously aligned regions, but also other sources of bias such as highly variable (saturated) characters, can improve the overall performance of many phylogenetic reconstruction methods. A current scientific trend is to build phylogenetic trees from a large number of sequence datasets (semi-)automatically extracted from numerous complete genomes. Because these approaches do not allow a precise manual curation of each dataset, there exists a real need for efficient bioinformatic tools dedicated to this alignment character trimming step.

Results

Here is presented a new software, named BMGE (Block Mapping and Gathering with Entropy), that is designed to select regions in a multiple sequence alignment that are suited for phylogenetic inference. For each character, BMGE computes a score closely related to an entropy value. Calculation of these entropy-like scores is weighted with BLOSUM or PAM similarity matrices in order to distinguish among biologically expected and unexpected variability for each aligned character. Sets of contiguous characters with a score above a given threshold are considered as not suited for phylogenetic inference and then removed. Simulation analyses show that the character trimming performed by BMGE produces datasets leading to accurate trees, especially with alignments including distantly-related sequences. BMGE also implements trimming and recoding methods aimed at minimizing phylogeny reconstruction artefacts due to compositional heterogeneity.

Conclusions

BMGE is able to perform biologically relevant trimming on a multiple alignment of DNA, codon or amino acid sequences. Java source code and executable are freely available at ftp://ftp.pasteur.fr/pub/GenSoft/projects/BMGE/.

Background

Most phylogenetic inference approaches are based on an alignment of homologous sequences (e.g. DNA, RNA, amino acids). The alignment of sequences aims at highlighting the substitutions that have occurred during the evolutionary process from their common ancestral sequence. The quality of a multiple sequence alignment can have a strong impact on the accuracy of the inferred phylogenetic tree, whatever the inference criterion used [1-4]. In spite of constant improvements of the multiple sequence alignment heuristics [5,6], an alignment can contain regions (i.e. sets of contiguous characters, also often called blocks [7,8]) where homology is ambiguous. Moreover, too divergent regions (even when correctly aligned) may induce a mutational saturation effect, which is an important source of bias for many phylogenetic reconstruction methods. In order to minimize the bias introduced by these problematic regions, a frequent approach is to detect and remove them from the multiple sequence alignment prior to phylogenetic analysis (e.g. [9-13]). Indeed, it has been observed that the removal of such regions allows more accurate trees to be inferred [7,8,14-16].

A current trend consists in reconstructing phylogenetic trees by using a large number of datasets of aligned sequences from many complete genomes. Phylogenetic trees are then reconstructed from these datasets in many contexts, such as the construction of gene tree databases [13], the inference of species trees based on a core-gene set [17,18] or the estimation of amino acid substitution matrices [19]. These different phylogenetic explorations are often based on (semi-)automated processes (e.g. [15,18,20]), requiring a software solution for each step of these computer pipelines. Given the importance of dataset quality, the use of practical and accurate software dedicated to alignment trimming task has become a real need.

In this paper, we present a novel software, named BMGE (Block Mapping and Gathering with Entropy), that identifies regions inside multiple sequence alignments that are suited for phylogenetic inference. BMGE computes a score for each character (i.e. amino acid, nucleotide or codon column), mainly determined by the entropy induced by the proportion of character states. To estimate realistic scores that take into account biologically relevant substitution processes (e.g. transition rates more frequent than transversions for DNA sequences, highest probability of changes between amino acids with physicochemical similarities), BMGE weights the entropy estimation with standard substitution matrices (e.g. PAM or BLOSUM). Averaging score values across the characters of the multiple sequence alignment allows identifying conserved (i.e. with low entropy-like score values) and highly variable/uncertain regions (i.e. with large entropy-like score values [15,21]). By removing such high entropy regions, BMGE returns trimmed datasets that allow the reconstruction of more accurate phylogenetic trees than the initial alignment, as shown by simulation studies.

In addition, BMGE also provides simple solutions to alleviate systematic artefacts caused by compositional heterogeneity. Most probabilistic phylogenetic inference methods make the assumption (among other more or less axiomatic ones) that the studied sequences arose from a common ancestral sequence following a stationary evolutionary process, i.e. the marginal probabilities of the character states remained constant over all sequences (e.g. [11,22]). Consequently, when phylogenetic trees are inferred from sequences with heterogeneous composition of character states, the violation of the stationary assumption may cause systematic errors [19,23-25]. BMGE is therefore able to perform RY-coding from a DNA sequence alignment [25], and to convert amino acid sequences into their corresponding degenerated codons according to the universal genetic code. These two recoding strategies may prove useful to minimize some biases when dealing with datasets with known heterogeneous composition across sequences. As these two recoding approaches use only the standard one-letter nucleotide alphabet [26] (see Table Table1),1), the resulting datasets can be given to all phylogeny inference programs, in contrast to alternative recoding techniques based on non-standard alphabet cardinality such as the "Dayhoff classes" 6-residue alphabet [27,28] (see also [29] for discussion on other recoding schemes). Moreover, the use of degenerated codons allow fast inference of trees, in particular with Maximum Likelihood (ML) methods which are faster with nucleotide sequences than with amino acid ones. BMGE also implements a novel stationary-based trimming method that allows compositionally heterogeneous characters to be identified and removed. To do so, BMGE uses the Stuart's χ2 matched-pairs test of marginal symmetry [30] that allows assessing the null hypothesis that two sequences are compositionally homogeneous [31], and iteratively performs character removal/addition steps until the Stuart's test assesses that each pair of sequences presents homogeneous composition. As shown by computer simulations with heterogeneous GC-content DNA sequences, this stationary-based trimming leads to unbiased phylogenetic trees.

Table 1
Character state coding used by BMGE

Implementation

Input/output files and sequence coding conversions

The input file for BMGE is a multiple sequence alignment in FASTA (or PHYLIP sequential) format. The user must indicate whether the sequences are amino acids or DNA (with standard one-letter coding [26,32]; see Table Table1).1). It is also possible to consider DNA sequences as codons, which allows the multiple sequence alignment to be handled with amino acid substitution matrices. Selected (and/or removed) regions are written in an output file in several formats (i.e. FASTA, PHYLIP sequential, NEXUS). HTML output is also available to display selected sites as well as graphical representation of both entropy values and gap proportions.

Several sequence conversion options are also available: from DNA or codons to RY-coding [25], and from codons to translated amino acids (according to the universal genetic code). BMGE also allows converting an amino acid alignment into a nucleotide alignment by considering the corresponding degenerated codons (see Table Table1).1). In practice, given an amino acid and its set of corresponding synonymous codons (following the universal genetic code), the degenerated codon is simply obtained, for each of the three codon positions p, by considering the nucleotides corresponding to the set of possible codons at position p. For example, isoleucine (I) can be encoded by the three codons ATA, ATC and ATT; therefore, the degenerated codon corresponding to this set of codons is ATH, knowing that the degenerated nucleotide H (i.e. A, C or T; see Table Table1)1) represents the possible nucleotides at the third threefold degenerate position.

Entropy-based character trimming

Given a multiple sequence alignment of m character length, BMGE computes, for each character c = 1,2,...,m , the frequency g(c) of gaps, as well as the diagonal matrix [product] (c) where each diagonal entry is the relative frequency of each of the r possible character states (r = 4 or 20, for DNA or amino acid sequences, respectively). So, BMGE computes the value h(c) for each character c, which is closely related to the von Neumann entropy [33] and is given by the following formula [34]:

h(c)=trace[μΠ(c)Slogr(μΠ(c)S)],
(1)

where S is a similarity matrix (see below for more details) and μ = [trace ([product](c)S) ]-1 is a normalizing factor so that trace (μ[product](c) S) = 1. To compute formula (1), BMGE uses the simpler equation

h(c)=s=1rλs(c)logrλs(c),
(2)

where the λs(c) parameters are the eigenvalues of the matrix μ[product](c)S estimated via the JAMA package [35]. It should be stressed that the entropy normalization condition s=1rλs(c)=1 is verified with the normalizing factor μ.

Knowing that h(c) = 0 indicates that character c is constant and that h(c) is as close to 1 as character c is unexpectedly variable (see below), BMGE looks for conserved regions of the multiple sequence alignment by smoothing the different h(c) values by using a sliding window of length 2w+1 (with w = 1 by default). For each c = 1, 2,...,m , the smooth An external file that holds a picture, illustration, etc.
Object name is 1471-2148-10-210-i11.gif value is estimated by the weighted average

h˜(c)=i=startend[1g(i)]h(i)i=startend[1g(i)],
(3)

with start = max(1;c-w) and end = min(m;c+w), in order to give more weight to characters with few gaps, i.e. g(c) [congruent with] 0. After this smoothing operation, BMGE defines as conserved those characters c that have An external file that holds a picture, illustration, etc.
Object name is 1471-2148-10-210-i11.gif value lower than a fixed threshold (0.5 by default). A conserved region is then defined as a set of contiguous conserved characters.

Then, the multiple sequence alignment is partitioned into successive conserved (C ) and variable (i.e. non-conserved; V ) regions, these being either a single character or a set of contiguous ones. Let Vi be the ith non-conserved region. By definition, Vi is flanked by the two conserved regions Ci and Ci+1. In order to distinguish variable regions due to ambiguous alignment from those due to natural variation, the average h˜ value is computed for the region Ci [union or logical sum] Vi[union or logical sum] Ci+1 by formula (3) with parameters 'start' and 'end' set as the first character of Ci and the last character of Ci+1, respectively. The consecutive regions Ci , Vi , Ci+1 with less than 30% of gaps and with h˜ value lower than the fixed 0.5 threshold are then merged into a unique conserved region. Finally, BMGE iteratively performs these merging operations until no more variable region Vi can be merged with its two flanking Ci and Ci+1 ones.

On the use of similarity matrix

If the similarity matrix S in formula (1) is the identity matrix Ir , then h(c) is closely related to the well-known Shannon entropy [36], given by formula (2) where each λs(c)=Πss(c) is simply the proportion of the character state s for character c. If the character c is constant, then h(c) = 0. On the other hand, if the character c is highly variable, then each of the r character states is present with a relatively high proportion (e.g. Πss(c)1/r), implying that h(c) is close to 1, its maximal value. Therefore, h allows the level of variability of a character to be quantified [21]. Unfortunately, using h with the identity matrix Ir (as suggested in [15]) suffers from biases. For example, when considering amino acid sequences, if a given character c1 is only made of the four residues I, L, M and V, each with 25% proportion, and a second character c2 is made of the four residues C, Q, W and Y, also with identical proportions, then formula (1) with matrix Ir returns h(c1) = h(c2) = -4× 0.25 log20 0.25 ≈ 0.462, and then indicates the same level of variability for both characters c1 and c2, while residues in character c1 are much more likely to be substituted than those in character c2 [27,37,38]. In contrast, using dedicated similarity matrices S I allows relevant substitution processes to be taken into account. As suggested in [34], when using the Henikoff and Henikoff's [39] BLOSUM50 target frequency matrix in formula (1), one obtains h(c1) ≈ 0.300 and h(c2) ≈ 0.453. Therefore, the function h with appropriate similarity matrix S computes score values that allow distinguishing among expected (i.e. biologically relevant) and ambiguous (e.g. source of noise) variability.

For practical use with amino acid sequences, BMGE provides the complete range of BLOSUM target frequency matrices (i.e. BLOSUM30, 35, 40, ..., 95 from [40]; see [39] for more details) in order to estimate pertinent h values depending on the level of divergence between sequences. As shown in simulation results (see below), our entropy-based character trimming method performs better when using stringent matrices (e.g. BLOSUM95) for closely related sequences, and, reciprocally, when using more relaxed matrices (e.g. BLOSUM30) for distantly related sequences. By default, BMGE uses the popular BLOSUM62 matrix [41].

For DNA sequences, PAM matrices are first computed. BMGE uses a transition/transversion ratio κ (= 2.0 by default) to compute the PAM-1 4 × 4 matrix: the four diagonal elements are all 0.99, and the off diagonal elements are 0.01 κ (2 + κ)-1 for transition and 0.01(2 + κ)-1 for transversion (see [42] for more details about the PAM-1 calculation for DNA). Given a prefixed integer η (= 100 by default), BMGE then computes the PAM-η matrix (= PAM-1η [27]), which is finally used by BMGE as similarity matrix S in formula (1). In a similar way as the previously described amino acid framework, our character trimming method is more accurate when using a stringent matrix (e.g. PAM-1) with closely related DNA sequences, and when using a relaxed matrix (e.g. PAM-250) with distantly related ones.

Stationary-based character trimming

Given two aligned sequences (e.g. taken from the multiple sequence alignment), one can use a r×r divergence matrix F to represent the relative proportion of each of the possible character state pairs in the pairwise comparison of these two sequences (as schematized for DNA sequences by formula (19) in [11]). If these two sequences have similar character state composition, then, for each character state s = 1, 2,...,r , this sequence pair verifies the null hypothesis Fs. = F.s , named the marginal homogeneity (e.g. [30,43]) or marginal symmetry (e.g. [31]). A not-too-low p-value returned by the Stuart's χ2 test [30] on F allows the marginal homogeneity/symmetry to be assessed; then, one can assess that two homologous sequences arise from a nonstationary evolutionary process if the Stuart's test returns a p-value close to zero (e.g. < 0.1). This test being essentially based on numerical linear algebra operations (see e.g. [31] for more details about its computation from two sequences), BMGE implements it with, on the one hand, matrix operations available in the JAMA package [35], and, on the other hand, with fast and accurate numerical algorithms for estimating χ2 cumulative distribution functions (adapted in Java from the C code sources available p. 216-219 in [44]).

If a multiple sequence alignment seems to be compositionally heterogeneous, BMGE implements a stationary-based character trimming in order to obtain a compositionally homogeneous alignment. Given a multiple alignment of n sequences, for each possible pair of distinct sequences i, j (i.e. 1 ≤ i <j n ), BMGE computes the Stuart's test p-value, denoted pij. If there is at least one pair of sequences for which pij < 0.1, then BMGE progressively removes the characters c ranked in function of their decreasing entropy-like h(c) values --as estimated by formula (1)-- until pij > 0.1 for every pairs of sequences i, j. This first crude character removal approach leads to a set C of compositionally homogeneous characters. Then, BMGE aims at integrating the set C with some of the previously removed characters, in order to obtain a set of compositionally homogeneous characters of maximal size.

To do so, BMGE uses an iterative add-and-remove approach of characters. Defining pij(c) as the Stuart's test p-value for the sequence pair i, j after adding the character c inside the set C, BMGE computes the following score for each character c [negated set membership] C :

σ(c)=1i<jnlog(pij(c)/pij).

If σ (c) > 0, then adding character c inside C leads to an increase for most of the n(n-1)/2 p-values; reciprocally, adding characters c with σ (c)< 0 leads to a (not wished) overall decrease of the p-values. BMGE then progressively removes the characters c [negated set membership] C from the initial multiple sequence alignment following the increasing order of their respective σ(c) value, i.e. from the smaller (negative) to the larger (positive) σ score value. After each character removal, every pij are re-estimated. When all pij > 0.1, BMGE stops removing characters from the initial alignment and considers the remaining (i.e. not removed) characters as the new set C. Finally, BMGE iteratively performs these add-and-remove operations until the set C of compositionally homogeneous characters cannot be increased further.

Results and Discussion

In order to assess the utility of multiple alignment character trimming to infer more accurate phylogenetic trees and to compare the respective performances of BMGE (with different similarity matrices) with other available character trimming methods (i.e. Gblocks [7]; Noisy [14]; trimAl [16]), we carried out computer simulations and real case studies. Protocol and results are described below.

Simulation results with entropy-based character trimming

The 200 first 40-taxon trees available in [45] were selected as model trees to generate artificial amino acid sequence datasets. On the one hand, in order to simulate phylogenetically informative characters, 10 clusters of 40 sequences each were generated using Seq-Gen [46] under the JTT model [47] from each of the 200 model trees. Sequence lengths for each of these 10 sequence clusters were randomly drawn from 30 to 70 amino acids. On the other hand, in order to simulate uninformative/variable characters, amino acid sequences were generated in the same way from a 40-taxon star tree (i.e. a tree with 40 leaves and a unique internal node).

Following these two steps, for each of the 200 initial model trees, we generated 20 clusters of 40 amino acid sequences of lengths 50 ± 20, ten containing informative phylogenetic signal, and ten containing uninformative/variable signal. Finally, from each of these 200 sets of 20 sequence clusters, 10 clusters were randomly drawn and concatenated, in order to produce a dataset composed of 200 clusters of 40 sequences of 500-amino acid length on average, each containing an equal mixture of phylogenetically informative and uninformative regions.

This simulation procedure to generate 200 clusters of sequences containing 50% (on average) of uninformative/variable characters was repeated three times, each with initial model tree branch lengths (see [45,48] for more details) multiplied by a divergence factor of 1, 2 and 3, respectively, in order to mimic from closely- to distantly-related sequence clusters. Each of these (3 × 200=)600 clusters of simulated amino acid sequences were aligned with MUSCLE [49,50]. The average lengths of these multiple sequence alignments are 513, 561, and 573 for the levels of divergence ×1, ×2, and ×3, respectively.

The software BMGE was applied on these multiple sequence alignments with three similarity matrices: BLOSUM30, BLOSUM62 and BLOSUM95. As a comparison, character trimming was also performed by using three available softwares.

Gblocks (0.91 b) was used with 'strict' and 'relaxed' parameter sets (see [7] for a precise description of these two parameter sets). However, the 'strict' conditions (default parameters in Gblocks) are indeed very stringent (e.g. no character was selected in ≈40% of the multiple sequence alignments with level of divergence ×3), and phylogenetic trees inferred from the remaining blocks (when these existed) were always less accurate than those inferred from the blocks returned by the 'relaxed' conditions (results not shown). Worse results than those obtained with the 'relaxed' conditions were also observed with alternative parameter sets (e.g. those described by [12]; results not shown). Then, results from Gblocks presented below are only those obtained with the 'relaxed' conditions.

The software Noisy was used with the --nogap options. Several other options were tested (especially the --cutoff one; see [14] for more details) but the Noisy default options allows better results to be observed with our simulated datasets.

The software trimAl (1.2rev59) allows three trimming methods (among numerous ones) to be used: 'gappyout', 'strictplus' and 'automated1'. Since the 'gappyout' method mainly focuses on highly gapped regions, this approach removed too few characters in our poorly gapped simulated datasets. Consequently, the 'gappyout' results are not shown since they are very close to those observed with the initial (i.e. non-trimmed) multiple sequence alignments.

As expected in regard to the sequence simulation protocol (see above), initial multiple sequence alignments returned by MUSCLE are composed of approximately 50% phylogenetically informative characters (i.e. those characters that are not generated by Seq-Gen from the star tree). For each trimming method, the character set of an initial multiple sequence alignment is then partitioned into four subsets: true positives and false negatives (i.e. phylogenetically informative characters that are selected or not by the trimming method, respectively), false positives (i.e. characters selected by the trimming method and that are not phylogenetically informative), and true negatives (i.e. characters that are not phylogenetically informative and are indeed not selected by the trimming method). Denoting tp and tn , the number of true positive and negative characters, respectively, and fp and fn , the number of false positive and negative characters, respectively, the true positive rate tpr = tp/(tp + fn) and false positive rate fpr = fp/(fp + tn) were computed. For each trimming method and each of the three levels of divergence (i.e. ×1, ×2, ×3), a ROC graph (e.g. [51-54]) depicting the plot of the true (y-axis) and false (x-axis) positive rates for each of the 200 datasets is represented in Figure Figure11.

Figure 1
ROC graphs plotting true (y-axis) and false (x-axis) positive rates for seven character trimming methods. The best methods (i.e., that minimize both the number of true negative and false positive characters) are those with the corresponding cloud concentrated ...

All initial (i.e. non-trimmed) multiple sequence alignments (i.e. tn = fn = 0) correspond to the (1,1) point (i.e. fpr = fp/fp = tpr = tp/tp =1); reciprocally, the removal of all characters (i.e. tp = fp = 0) corresponds to the (0,0) point (i.e. fpr = 0/tn = tpr = 0/fn = 0). A cloud close to the (1,1) point in the ROC graph then indicates that the corresponding trimming method is liberal (i.e. it keeps too many uninformative/variable characters). Conversely, conservative trimming methods (i.e. that remove too many phylogenetically informative characters) correspond to clouds close to the (0,0) point. Ideally, the best method selects only those characters that are phylogenetically informative (i.e. fn = fp = 0), and then corresponds to the (0,1) point inside the ROC graph (i.e. fpr = 0/tn = 0 and tpr = tp/tp = 1). For each case in Figure Figure1,1, the L1 distance between each point and the (0,1) point (= 1-tpr+fpr ) was computed, averaged and written under its ROC graph. For each of the three levels of divergence (i.e. ×1, ×2, ×3), a sign test [55-57] was performed to assess the statistical significance between the best average L1 distance measure (i.e. the lowest) and the other ones. For each level of divergence in Figure Figure1,1, an average L1 distance measure is considered as non-significantly different to the best one if the p-value returned by the sign test is > 5%.

Figure Figure11 shows that, in all cases, trimAl has always tpr ≈ 1 but often fpr [dbl greater-than sign] 0, indicating that it is too liberal (i.e. fp [dbl greater-than sign] 0); moreover, L1 distances observed for trimAl are often among the worst, similarly to those observed for Noisy (except for the level of divergence ×3). We can also see from Figure Figure11 that Gblocks with relaxed conditions presents very good performance with closely related sequences (i.e. level of divergence ×1), but induces tpr «1 when the level of divergence increases (i.e. from ×1 to ×3), showing that it becomes too conservative (i.e. fn [dbl greater-than sign] 0). As expected, BMGE with stringent option (i.e. BLOSUM95) corresponds to points that are more concentrated around the y-axis as the level of sequence divergence increases, showing that the use of stringent similarity matrices such as ranging from BLOSUM80 to BLOSUM95 lead to conservative character trimming with distantly related sequences (e.g. level of divergence ×3). Reciprocally, the use of the similarity matrix BLOSUM30 leads to selecting too many characters (i.e. fpr [dbl greater-than sign] 0) with closely related sequences (i.e. level of divergence ×1). However, BMGE with BLOSUM30 allows minimizing both fn and fp when the level of divergence increases; indeed this last BMGE usage leads to the best average L1 distances for the levels of divergence ×2 and ×3.

Simulation results on phylogenetic tree accuracy

For each of the three levels of divergence and from each multiple sequence alignment (i.e. the initial one as well as those outputted by BMGE, Gblocks, Noisy and trimAl), phylogenetic trees were inferred with several approaches. Maximum Likelihood (ML) trees were inferred by PhyML [48] with model JTT-Γ4. BioNJ [58] trees were also inferred by PhyML with JTT distances. Maximum Parsimony (MP) trees were inferred by TNT [59] with TBR branch swapping and parsimony ratchet [60]. Bayesian inference was not performed because of the huge running time required by this approach. Moreover, Bayesian trees are expected to be very close to ML trees when inferred from our simulated datasets [3].

For each of the three levels of divergence, topological accuracy of the ML, BioNJ and MP trees inferred from the initial and the trimmed multiple sequence alignments was measured by the quartet distance [61] between each inferred tree and its corresponding model tree. All these distance measures are reported in Tables Tables2,2, ,33 and and44 for ML, BioNJ and MP trees, respectively, normalized in order to restrict these values to the interval [0,1], then averaged. For each of the three levels of divergence (i.e. ×1, ×2, ×3) and each of the three tree reconstruction methods (i.e. ML, BioNJ, MP), a sign test was performed to assess the statistical significance between the best average distance measure (i.e. the lowest) and the other ones. In each column of the Tables Tables2,2, ,33 and and4,4, an entry is considered as non-significantly different to the best one if the p-value returned by the sign test is > 5%.

Table 2
Average quartet distances between the model trees and the ML trees inferred from the different trimmed multiple sequence alignments
Table 3
Average quartet distances between the model trees and the BioNJ trees inferred from the different trimmed multiple sequence alignments
Table 4
Average quartet distances between the model trees and the MP trees inferred from the different trimmed multiple sequence alignments

Variable/uncertain characters contained in the initial multiple sequence alignments cause strong artefacts in the resulting phylogenetic trees, especially for BioNJ and MP trees (see Tables Tables2,2, ,3,and3,and ,and4).4). When character trimming softwares are used, almost all reconstructed phylogenetic trees are closer to their model tree (Tables (Tables2,2, ,3,3, and and4),4), showing that character trimming is a useful step prior any phylogenetic inference. However, it should be stressed that the ML approach is very robust to the noise introduced by uninformative/variable characters in our simulated datasets, mainly thanks to the Γ parameter. Even if our datasets were generated with equal rates across characters (see above), estimation of a Γ parameter was included in ML inference because preliminary tries without Γ parameter led to less accurate trees, especially those inferred from Noisy and trimAl outputs (results not shown). The Γ parameter then helps to compensate part of the phylogenetic noise contained in our datasets. However, when considering distantly-related sequences (e.g. level of divergence ×3), the ML approach (as well as the BioNJ and MP ones) needs a preliminary trimming step to infer significantly accurate trees, in agreement with results from previous simulation-based studies (e.g. [8]).

In general, BMGE (when used with a BLOSUM substitution matrix adequate to the level of sequence divergence) allows reconstructing among the most accurate trees for each of the three levels of divergence and every tree reconstruction method used (Tables (Tables2,2, ,33 and and4).4). trimAl and Noisy infer the worst BioNJ and MP trees, whereas Gblocks with relaxed conditions produces good results as long as sequences are not too divergent. To the minor exception of Noisy with ML trees, BMGE trimming with the (less stringent) BLOSUM30 matrix allows reconstructing the significantly best trees with level of divergence ×3.

Simulation results on phylogenetic tree branch support

In order to observe the impact of character trimming methods on branch supports inside phylogenetic trees, we have focused on two different approaches to estimate confidence values on the internal branches of a phylogenetic tree: the bootstrap-based support [62] with BioNJ trees, and the approximate likelihood ratio test (aLRT; [63]) as implemented by default in PhyML 3.0 [64].

For each of the three levels of divergence (i.e. ×1, ×2, ×3) and from each multiple sequence alignment (i.e. the initial as well as the seven outputted by BMGE, Gblocks, Noisy and trimAl; see above), 100 bootstrap-based replicates were generated, and 100 BioNJ trees were inferred from these multiple sequence alignment replicates. From these 100 BioNJ bootstrap-based trees, bootstrap proportions were assessed on the internal branches of the corresponding (true) model tree. For each character trimming method and each level of divergence, we computed the distribution of the so-obtained bootstrap-based confidence values, as well as its average value (Figure (Figure2).2). Similarly, we also computed the distributions of aLRT branch support estimated on the (true) branches of the model trees from the different multiple sequence alignments, as well as their average values (Figure (Figure3).3). For each way to estimate confidence values (i.e. BioNJ bootstrap-based and aLRT-based ones) and each level of divergence (i.e. ×1, ×2, ×3), a χ2 test was performed to assess whether distributions are significantly different. In Figures Figures22 and and3,3, a distribution is considered as non-significantly different to the best one (i.e. those corresponding to the highest average confidence value) if the p-value returned by the χ2 test is > 5%.

Figure 2
Distributions of the BioNJ bootstrap-based confidence values on the true branches of model trees estimated from initial (non-trimmed) multiple sequence alignments and from alignments returned by seven character trimming methods. Average confidence values ...
Figure 3
Distributions of the aLRT confidence values on the true branches of model trees estimated from initial (non-trimmed) multiple sequence alignments and from alignments returned by seven character trimming methods. See Figure 2.

For each of the three levels of divergence and from each multiple sequence alignment, BioNJ-based bootstrap proportions were also estimated on the branches of the phylogenetic trees inferred by BioNJ (i.e. those used to compute quartet distances in Table Table3).3). A bootstrap-based confidence value is then expected to be high when the corresponding branch is true (i.e. present in the model tree), and is expected to be low for false branches. Given a threshold τ, all branches of an inferred tree can be partitioned into four subsets: true positives or false negatives (i.e. true branches with confidence values ≥ τ or <τ, respectively), false positives or true negatives (i.e. false branches with confidence values ≥ τ or <τ, respectively). As a consequence, there exists a point in the ROC space (see above) that is associated to a threshold value τ, and plotting these points for a large number of possible threshold values τ results in a so-called ROC curve (see [52,54] for more details). ROC curves obtained by varying τ from 0 to 1 with 0.02-increment are displayed in Figure Figure4,4, where up-right head of each ROC curve corresponds to lowest τ values, whereas down-left tail corresponds to highest τ values. Figure Figure55 represents ROC curves built in the same way from aLRT-based confidence values on the branches of the inferred ML trees (i.e. those used to compute quartet distances in Table Table2).2). Figure Figure44 and and55 also display the area under each ROC curve (AUC) that corresponds to the probability that a confidence value will be higher for a true branch than for a false branch (see [65,54] for more details). For each of the three levels of divergence, a Z test (as described in [66]) was performed to assess the statistical significance between the best AUC (i.e. the highest) and the other ones. In Figures Figures44 and and5,5, an AUC is considered as non-significantly different to the best one if the p-value returned by the Z test is > 5%.

Figure 4
ROC curves constructed by thresholding BioNJ bootstrap-based confidence values. Best tree branch classifiers (i.e., that are able to associate higher confidence values to true branches than to false branches) are those that maximize the area under the ...
Figure 5
ROC curves constructed by thresholding aLRT-based confidence values. See Figure 4.

Broadly, Figure Figure22 shows that the estimate of BioNJ bootstrap proportions from the initial (non-trimmed) multiple sequence alignments leads to very biased values, with a proportion of true branches with bootstrap-based confidence values ≤ 0.1 varying from 31% to 47%, and those > 0.9 varying from 18% to 20%. Figure Figure22 also shows that the highest average bootstrap-based confidence values are obtained from the character-trimming methods that best optimize both tpr and fpr criteria (see above and Figure Figure1).1). The same conclusions hold for aLRT with level of divergence ×1 (Figure (Figure3),3), with (significantly) best average aLRT values observed with BMGE and Gblocks. Surprisingly, for level of divergence ×3, the best average aLRT values are obtained from the characters selected by the most liberal character trimming methods, i.e. initial alignments and trimAl (strictplus and automated1).

AUC values in Figures Figures44 and and55 show that initial (non-trimmed) multiple sequence alignments lead to more incorrect confidence values than those estimated from characters selected by trimming methods. Interestingly, Figures Figures44 and and55 show that aLRT-based ROC curves induce highest AUC values on average that bootstrap-based ones (with the slight exception of BMGE with BLOSUM95 for level of divergence ×3). This shows that aLRT-based confidence values are more able to discreminate true and false branches than BioNJ bootstrap-based ones. ROC curve shapes also show that trimming methods lead to more precise confidence values. Indeed, in Figure Figure4,4, the down-left tail point of each ROC curve (i.e. corresponding to threshold τ = 0.98) always has highest tpr (y-axis) for trimmed alignments than for initial ones; this shows that a larger proportion of true branches with BioNJ bootstrap-based confidence values >0.98 is observed with trimmed alignments than with initial alignments. For initial multiple sequence alignments and for level of divergence ×2 and ×3 in Figure Figure4,4, the up-right head points of these two ROC curves (i.e. each corresponding to threshold τ = 0.02) have tpr < 1; this means that there exists some true branches with BioNJ bootstrap-based confidence value < 0.02. Notably, this is not the case when using character trimming methods. These two tendencies on tpr values for both extremities of the ROC curves are in agreement with the distributions in Figure Figure2.2. Nevertheless, when observing the fpr ranges (x-axis) of the ROC curves in Figure Figure4,4, trimmed multiple sequence alignments all induce larger fpr values than initial ones; this shows that when using character trimming methods instead of initial multiple sequence alignments, there is an increase in the proportion of false branches in BioNJ trees with high confidence value (e.g. down-left tail of ROC curves corresponding to τ = 0.98) and a decrease of the proportion of false branches with low confidence values (e.g. up-right tail of ROC curves corresponding to τ = 0.02). This last tendency is clearly obvious with level of divergence ×3 (see Figure Figure4).4). However, shapes of ROC curves constructed by thresholding aLRT-based confidence values on ML trees do not seems to be strongly modified by trimming methods (see Figure Figure5).5). More precisely, for levels of divergence ×1 and ×2, Gblocks and BMGE (with BLOSUM62) present always among the best results. For level of divergence ×3, Noisy and BMGE with BLOSUM30 present the significantly best AUC values for aLRT-based confidence values.

To sum up, these simulation results show that, by selecting among variable characters those with biologically-relevant expected variability thanks to the use of similarity matrices, BMGE often presents results that are among the (significantly) best (e.g. phylogenetic accuracy, better confidence values for true branches) and leads to a less biased phylogenetic signal.

Entropy-based character trimming in a phylogenomics context

In order to illustrate the benefit of using character trimming approaches, we have re-analysed the multi-gene dataset used by Castresana (2000) to describe the usefulness of Gblocks [7] in selecting suited characters. This amino-acid dataset is composed by ten genes (i.e. three subsunits of cytochrome c oxidase CO1-CO3, one subunit of cytochrome c-ubiquinol oxidoreductase CYTb, and six subunits of NADH desydrogenase ND1-ND5 and ND4L) gathered from the complete mitochondrial genome of 16 eukaryotes (11 unikonts, 4 archaeplastida, 1 excavate), and from Paracoccus denitrificans, an α-proteobacterium used as outgroup (see [7] for more details).

Protein sequences were aligned with MUSCLE, and each of the 10 multiple sequence alignments were trimmed by BMGE, Gblocks, trimAl and Noisy with the same parameters used in the previous simulations. For each of these seven character trimming approaches as well as the initial (non-trimmed) multiple sequence alignment, the ten so-obtained character matrices were concatenated into a single character supermatrix with the software Concatenate [67]. Table Table55 shows the different number of characters of these eight supermatrices. ML trees were inferred with PhyML from each character supermatrix with the mtREV model of amino acid substitution [68]. Parameters defining the shape of the Γ distribution (8 categories) and the proportion of invariable characters were both left as free. The different log-likelihood (log-lk) estimated for each inferred ML trees were normalized by the total number of characters for better comparison and are shown in Table Table5.5. ML bootstrap-based (100 replicates) and aLRT confidence values were assessed on the branches of the different inferred trees.

Table 5
Lengths of the different character supermatrices, and average log-likelihood per character of the corresponding ML trees.

It should be stressed that our initial character supermatrix (i.e. 4,530 characters; see Table Table5)5) is slightly larger than the number of characters inside the original character supermatrix in [7] (i.e. 4,453); this is due to the use of different multiple sequence alignment softwares. It should also be stressed that the log-lk per character estimated from our initial character supermatrix (i.e. -21.07; see Table Table5)5) is higher than those provided in [7] (i.e. -22.71; see Table Table4,4, page 546 in [7]); this can be explained by the different number of characters but also by our use of the amino acid model mtREV+Γ8+I instead of just mtREV in [7]. However, the ML tree inferred from our initial character supermatrix has the same topology (left-hand tree in Figure Figure6)6) as the ML tree inferred by Castresana (2000; see Figure Figure5A,5A, page 545 in [7]). The use of BMGE (with default BLOSUM62 and liberal BLOSUM30 matrices), Gblocks (relaxed), trimAl (strictplus and automated1) and Noisy lead to the same phylogenetic tree (left-hand tree in Figure Figure6).6). However, BMGE with the stringent BLOSUM95 similarity matrix leads to a different ML phylogenetic tree (right-hand tree in Figure Figure6).6). These two trees agree on the monophyly of Unikonts (nodes 1 and 1' in Figure Figure6),6), but differ in the placement of the jacobid Reclinomonas americana, which is inside the Archaeplastida subtree in the left-hand tree of Figure Figure6.6. Knowing that Archaeplastida and Unikonts are each likely monophyletic, and that jacobids are phylogenetically distinct from Archaeplastida (e.g. [69-72]), the BMGE (with BLOSUM95) tree at the right-hand side in Figure Figure66 seems more accurate. Moreover, BLOSUM95-based character trimming in BMGE gives among the best confidence values for the monophyly of Unikonts whereas Gblocks and trimAl both weakly support this subtree (see confidence values for nodes 1 and 1' in Table Table6).6). The monophyly of Archaeplastida is weakly supported by all approaches, suggesting that this dataset does not induces sufficient phylogenetic signal for this particular node. However, BMGE with BLOSUM95 seems to provide a character trimming that leads to both accurate phylogenetic tree and confidence values, probably due to its ability to best minimize the number of false positive characters (see above and Figure Figure11).

Table 6
ML bootstrap-based (boot.) and aLRT-based confidence values derived from different character supermatrices.
Figure 6
Phylogenetic trees obtained from a non-trimmed character supermatrix (left) and from the concatenation of the multiple sequence alignments trimmed by BMGE with BLOSUM95 (right). These ML trees were inferred by PhyML with the model mtREV+Γ8+I. ...

This re-analysis of a known phylogenomic dataset shows that it is quite difficult to choose an appropriate similarity matrix with BMGE, knowing that, in the one hand, these mitochondrial amino acid sequences are distantly related (see [7]), and that, in the other hand, a less unrealistic tree is inferred when BMGE is used with the stringent BLOSUM95 similarity matrix. To deal with amino acid sequences and BLOSUM matrices, a trivial approach would be to use the sequence clustering rule defined by Henikoff and Henikoff [39]: to compute the BLOSUMη similarity matrix, they grouped amino acid sequences into clusters in such a way that each sequence in any cluster has at least η% identity to at least one other sequence in this cluster. Given an alignment with n amino acid sequences, a systematic procedure to choose the BLOSUM η similarity matrix is then to apply the following formula:

η=mini=1,2,,nmaxj=1,2,,i1,i+1,,n{%identitybetweensequencesiandj}
(4)

Unfortunately, this formula underestimates the value of η that best minimizes both the number of false positive and negative characters in our simulated datasets, e.g. η, as estimated by (4), varies from 16 to 71 with an average of 33 with level of divergence ×1, and varies from 10 to 62 with an average of 22 with level of divergence ×3, whereas simulation shows that best results are obtained with η = 95 and 30 for levels of divergence ×1 and ×3, respectively. Indeed, formula (4) on the Castresana (2000) phylogenomic dataset gives η values varying from 34 (ND3) to 64 (CO1), which shows that the amino acid sequences constituting these ten alignments are not closely related, whereas we have shown that the conservative BLOSUM95 similarity matrix is best adapted than BLOSUM62 and BLOSUM30 ones. Moreover, when estimated by (4) from the eight considered character supermatrices, η varies from 52 (concatenated initial multiple sequence alignments) to 60 (concatenated alignments trimmed by Noisy). A similar underestimation of η was also observed by averaging the n max values in formula (4), or by considering only characters with no gaps. Finally, even if formula (4) or related could give a suited approximate of the η value by using the building rules of BLOSUM matrices, it will be even more difficult to provide a similar formula for the PAM-η similarity matrices when dealing with DNA sequences.

Therefore, as maintained by Ewens and Grant (2005) for BLAST queries, we believe that "one often has prior knowledge about the evolutionary distance between the sequences of interest that helps one choose which BLOSUM matrix to use" (p. 244 in [73]). In practice, when inferring a particular gene tree, our opinion is to carefully examine the original multiple sequence alignment and those obtained by BMGE trimming with several similarity matrices (i.e. BLOSUM or PAM). On the contrary, when building a phylogenomic dataset, we believe, as Talavera and Castresana (2007), that "there is enough information from the concatenation of several genes" and then that "stringent conditions tend to give rise to the best phylogenetic trees" (p. 575 in [7]): the use of BMGE with stringent similarity matrices (e.g. BLOSUM95 or PAM-1) can strongly increase the number of false negatives (i.e. too many characters suited for phylogenetic inference are removed; see Figure Figure1)1) but systematic biases due to this conservative approach are often compensated by a sufficiently large number of genes used. Finally and in every case, we think that it is more relevant to deal with well-defined similarity matrices in order to choose among stringent to relaxed character trimming as in BMGE, rather than having to set several (and subjective) numerical parameters.

Simulation results with stationary-based character trimming

We illustrate the impact of compositional heterogeneity and stationary-based character trimming on the accuracy of phylogenetic tree inference with a simple computer simulation. Given the quartet tree in Figure Figure7,7, the evolution of a DNA sequence of length 10,000 with 25%-proportion of each nucleotide was simulated by Seq-Gen from the root to the four leaves u, v, x and y. To infer the evolution of this DNA sequence, the evolutionary model F81 [74] was chosen. On the one hand, Seq-Gen was used with equal relative character state frequencies to generate a compositionally homogeneous region (i.e. from 100% to 50% of the total length, with 10% increments). On the other hand, to generate a compositionally heterogeneous region (i.e. from 0% to 50% of the total length, respectively), DNA evolution was simulated with 80% GC-content for the external branches corresponding to the taxa u and x, and 20% GC-content for the two other external branches (i.e. taxa v and y). For each proportion of characters with heterogeneous composition (i.e. 0%, 10%, ..., 50% of the length of the alignment), 500 four-sequence alignments were generated following this procedure.

Figure 7
Phylogenetic tree used to simulate the non-stationary evolution of a DNA sequence. This tree and the different branch lengths are closely related to [24].

ML trees were inferred with PhyML (model F81) from all these simulated alignments. Stationary-based character trimming was applied with BMGE, and ML trees were inferred from the resulting compositionally homogeneous alignments. For each of the five proportions (i.e. 0%, 10%, ..., 50%) of unequal GC-content characters, the number of times that the model tree (Figure (Figure1)1) was correctly inferred from both initial and trimmed alignments is graphically represented in Figure Figure8.8. The average proportions of characters removed by the stationary-based trimming are also reported. As expected [24], the model tree is often recovered with the initial alignments when these contain no or a small proportion of compositionally heterogeneous characters (e.g. < 20% of the total length of the initial alignment; see Figure Figure8),8), whereas the model tree is much less or not recovered when there is a high overall GC-content in taxa u and x, causing a biased attraction between them [25]. Thanks to the stationary-based character trimming, BMGE detects and removes regions that are compositionally heterogeneous; then, as shown in Figure Figure8,8, the model tree is very often recovered (e.g. the model tree is correctly inferred from more than 90% of the trimmed alignments), even when the proportion of unequal GC-content characters across sequences is high (e.g. > 30% of the total length of the initial alignment).

Figure 8
Frequency of recovered model tree in function of the proportion of regions with heterogeneous composition inside an alignment of four DNA sequences.

There exist many alternative statistical solutions to compare the character state composition of two (or more) sequences. Each of these has its own strengths and weaknesses (see [24] for instructive survey and discussion). However, matched-pairs tests (such as Stuart's test [30]) are comparatively efficient, particularly because of their ability to consider aligned sequences on a site-by-site basis [24]. Albeit the stationary-based character trimming may be extended by the use of overall tests for marginal symmetry (i.e. assessing the compositional homogeneity in the complete multiple sequence alignment [75,31]), we think that using pairwise p-values allows more precise sorting of the characters c according to their σ(c) score value (see above). Moreover, such overall tests are more time consuming. It should also be stressed that the Bowker's [76] test (i.e. another matched-pairs test assessing the complete symmetry inside F) was tried instead of the Stuart's test in the stationary-based trimming, but it led to worse results in the simulation analysis (not shown). Finally, as stressed in [43], Stuart's test is based on ordinary χ2 approximation and is not appropriate for small samples, particularly when the number of categories (i.e. the row number in F) is not small. It is then strongly recommended to use the stationary-based character trimming on a large number of characters (e.g. ≥ 1, 000, such as in supermatrices of characters), especially when dealing with amino acid sequences.

Real case study with stationary-based character trimming

In order to illustrate the performance of the stationary-based character trimming, we applied it on the multi-gene dataset described in [77] (available at [78]), which is known to suffer from a GC-content bias. This phylogenomic dataset was built by concatenating 106 alignments of DNA sequences gathered from 7 Saccharomyces species and Candida albicans as outgroup (see [77] for more details). The so-obtained supermatrix contains 127,026 nucleotide characters.

By using on this character supermatrix the same methods and software as Phillips, Delsuc and Penny (2004; see [25] for more details), we retrieved the same phylogenetic tree (left-hand tree in Figure Figure9)9) by minimizing the Minimum Evolution (ME) criterion with both GTR [79-81] and LogDet [82-84] distance estimates. We also retrieved the same ME bootstrap-based confidence values as in [25], i.e. 100% bootstrap proportion at all branches. Nevertheless, as shown by numerous phylogenetic analyses of the same dataset (e.g. [77,25,85-89]), this tree is incorrect: the real evolutionary history of these 8 yeast taxa is in fact the right-hand tree in Figure Figure9,9, with no monophyletic relationship between S. kudriavzevii and S. bayanus. It was shown in [25] that this systematic bias is due to a GC-content compositional heterogeneity across sequences that is sufficiently important to mislead the ME criterion.

Figure 9
Phylogenetic trees inferred before (left) and after (right) stationary-based character trimming. Both trees are inferred by minimizing the Minimum Evolution criterion with GTR and LogDet distance estimations. ME bootstrap-based confidence values at branches ...

A subset of 114,105 characters was selected by stationary-based character trimming implemented in BMGE. These so-selected characters were used to infer ME trees following the same methods as described previously. As expected, the right-hand tree in Figure Figure99 was inferred from both GTR and LogDet distance estimates with 100% bootstrap-based confidence value at each branch. More precisely, pairwise Stuart's test p-values are all ≈ 0 in the initial character supermatrix (with the slight exception of the two sequence pairs S. cerevisiae - S. paradoxus and S. cerevisiae - S. mikatae with p-values of 0.0146 and 0.0868, respectively). After the stationary-based trimming performed by BMGE, all Saccharomyces sequences induce pairwise Stuart's test p-values > 0.85, the lowest p-values being induced by the outgroup species (i.e. varying from 0.1000 to 0.3675 for the sequence pairs C. albicans - S. kluyveri and C. albicans - S. castellii, respectively). This shows that by removing 10% characters, the stationary-based trimming is able to select a subset of compositionally homogeneous characters (as assessed by the pairwise Stuart's tests) that leads to unbiased ME phylogenetic inference.

Conclusions

There exists a real need for accurate bioinformatic tools to extract at best the phylogenetic information contained in the ever-growing amount of available genomic sequence data. BMGE allows accurate character trimming of multiple alignments of DNA, codon, or amino acid sequences based on entropy-like scores weighted with BLOSUM or PAM matrices. Thus, BMGE is able to identify and extract unambiguously aligned blocks of characters that contain biologically expected variability and are therefore suitable for phylogenetic analysis. Simulation studies show that the trimmed datasets returned by BMGE lead to inference of accurate trees, in particular when in presence of multiple alignments including distantly-related sequences. BMGE also allows a number of useful recoding and trimming aimed at minimizing compositional heterogeneity in the alignment dataset and therefore the risk of phylogenetic artefacts.

In conclusion, BMGE is an accurate tool that can have several applications in phylogenomics analyses. The software BMGE is freely available (see below), and can also be used online through the Mobyle Web Portal [90] at http://mobyle.pasteur.fr/cgi-bin/portal.py.

Availability and Requirements

• Project name: Block Mapping and Gathering with Entropy (BMGE)

• Project home page: ftp://ftp.pasteur.fr/pub/GenSoft/projects/BMGE/

• Operating systems: Platform independent

• Programming language: Java

• Other requirements: Java 1.6 or higher

• License: GNU General Public License (version 2)

• Any restrictions to use by non-academics: None

Authors' contributions

AC initiated the project, designed and implemented the different methods inside the software, performed the computer simulations, and wrote the manuscript. SG supervised the project, and participated in designing the entropy-based character trimming method and in writing the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We thank Céline Petitjean, Elie Desmond, Céline Brochier and two anonymous reviewers for their comments and for testing the program, as well as the BMGE team for support. Many thanks to Corrine Maufrais for providing us with an ftp home page, and for placing BMGE in the Mobyle portal. This research was supported by the PhyloCyano project of the Agence Nationale de la Recherche (ANR; 07-JCJC-0094-01).

References

  • Lake JA. The order of sequence alignment can bias the selection of tree topology. Mol Biol Evol. 1991;8:378–385. [PubMed]
  • Morrison DA, Ellis JT. Effects of nucleotide sequence alignment on phylogeny estimation: a case study on 18 S rDNAs of apicomplexa. Mol Biol Evol. 1997;14:428–441. [PubMed]
  • Ogden TH, Rosenberg MS. Multiple sequence alignment accuracy and phylogenetic inference. Syst Biol. 2006;55:314–328. doi: 10.1080/10635150500541730. [PubMed] [Cross Ref]
  • Wang L-S, Leebens-Mack J, Wall PK, Beckmann K, dePamphilis CW, Warnow T. The impact of multiple protein sequence alignment on phylogenetic estimation. IEEE/ACM Trans Comput Biol Bioinf. 2009. in press . [PubMed]
  • Edgar RC, Batzoglou S. Multiple sequence alignment. Curr Opin Struct Biol. 2006;16:368–373. doi: 10.1016/j.sbi.2006.04.004. [PubMed] [Cross Ref]
  • Notredame C. Recent evolutions of multiple sequence alignment algorithms. PLoS Comput Biol. 2007;3:e123. doi: 10.1371/journal.pcbi.0030123. [PMC free article] [PubMed] [Cross Ref]
  • Castresana J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol Biol Evol. 2000;17:540–552. [PubMed]
  • Talavera G, Castresana J. Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst Biol. 2007;56:564–577. doi: 10.1080/10635150701472164. [PubMed] [Cross Ref]
  • Olsen GJ, Woese CR. Ribosomal RNA: a key to phylogeny. FASEB J. 1993;7:113–123. [PubMed]
  • Rodrigo AG, Bergquist PR, Bergquist PL. Inadequate support for an evolutionary link between the Metazoa and the Fungi. Syst Biol. 1994;43:578–584.
  • Swofford DL, Olsen GJ, Waddell PJ, Hillis DM. In: Molecular Systematics. Hillis DM, Moritz C, Mable BK, editor. Sunderland: Sinauer Associates; 1996. Phylogenetic inference; pp. 407–514.
  • Rodríguez-Ezpeleta N, Brinkmann H, Burey SC, Roure B, Burger G, Löffelhardt W, Philippe H, Lang BF. Monophyly of primary photosynthetic eukaryotes: green plants, red algae, and glaucophytes. Curr Biol. 2005;15:1325–1330. doi: 10.1016/j.cub.2005.06.040. [PubMed] [Cross Ref]
  • Huerta-Cepas J, Bueno A, Dopazo J, Gabaldón T. PhylomeDB: a database for genome-wide collections of gene phylogenies. Nucleic Acids Res. 2008;36:D491–D496. doi: 10.1093/nar/gkm899. [PMC free article] [PubMed] [Cross Ref]
  • Dress AWM, Flamm C, Fritzsch G, Grünewald S, Kruspe M, Prohaska SJ, Stadler PF. Noisy: Identification of problematic columns in multiple sequence alignments. Algorithms for Molecular Biology. 2008;3:7. doi: 10.1186/1748-7188-3-7. [PMC free article] [PubMed] [Cross Ref]
  • Swingley WD, Blankenship RE, Raymond J. Integrating Markov clustering and molecular phylogenetics to reconstruct the cyanobacterial species tree from conserved protein families. Mol Biol Evol. 2008;25:643–654. doi: 10.1093/molbev/msn034. [PubMed] [Cross Ref]
  • Capella-Gutiérez S, Silla-Martínez JM, Gabaldón T. trimAl: a tool for automated alignment triming in large-scale phylogenetic analyses. Bioinformatics. 2009;25:1972–1973. doi: 10.1093/bioinformatics/btp348. [PMC free article] [PubMed] [Cross Ref]
  • Daubin V, Gouy M, Perrière G. A phylogenomic approach to bacterial phylogeny: evidence of a core of genes sharing a common history. Genome Res. 2002;12:1080–1090. doi: 10.1101/gr.187002. [PMC free article] [PubMed] [Cross Ref]
  • Ciccarelli FD, Doerks T, von Mering C, Creevey CJ, Snel B, Bork P. Toward automatic reconstruction of a highly resolved tree of life. Science. 2006;311:1283–1287. doi: 10.1126/science.1123061. [PubMed] [Cross Ref]
  • Adachi J, Waddell PJ, Martin W, Hasegawa M. Plastid genome phylogeny and a model of amino acid substitution for protein encoded by chloroplast DNA. J Mol Evol. 2000;50:348–358. [PubMed]
  • McMahon MM, Sanderson MJ. Phylogenetic supermatrix analysis of GenBank sequences from 2228 Papilionoid legumes. Syst Biol. 2006;55:818–836. doi: 10.1080/10635150600999150. [PubMed] [Cross Ref]
  • Schneider TD, Stephens RM. Sequence logos: a new way to display consensus sequences. Nucl Acids Res. 1990;18:6097–6100. doi: 10.1093/nar/18.20.6097. [PMC free article] [PubMed] [Cross Ref]
  • Jayaswal V, Jermiin LS, Robinson J. Estimation of phylogeny using a general Markov model. Evol Bioinf Online. 2005;1:62–80. [PMC free article] [PubMed]
  • Galtier N, Gouy M. Inferring pattern and process: maximum-likelihood implementation of a nonhomogeneous model of DNA sequence evolution for phylogenetic analysis. Mol Biol Evol. 1998;15:871–879. [PubMed]
  • Jermiin LS, Ho SYW, Ababneh F, Robinson J, Larkum AWD. The biasing effect of compositional heterogeneity on phylogenetic estimates may be underestimated. Syst Biol. 2004;53:638–643. doi: 10.1080/10635150490468648. [PubMed] [Cross Ref]
  • Phillips MJ, Delsuc F, Penny D. Genome-scale phylogeny and the detection of systematic biases. Mol Biol Evol. 2004;21:1455–1458. doi: 10.1093/molbev/msh137. [PubMed] [Cross Ref]
  • International Union of Pure and Applied Chemistery and International Union of Biochemistery (IUPAC-IUB) Commission on Biochemical Nomenclature. Abbreviations and symbols for nucleic acids, polynucleotides and their constituents. Biochem J. 1970;120:449–454. [PMC free article] [PubMed]
  • Dayhoff MO, Schwartz RM, Orcutt BD. In: Atlas of Protein Sequence and Structure. Suppl 3. Dayhoff MO, editor. Vol. 5. Washington: National Biomedical Research Foundation; 1978. A model of evolutionary change in proteins; pp. 345–352.
  • Embley TM, van der Giezen M, Horner DS, Dyal PL, Foster P. Mitochondria and hydrogenosomes are two forms of the same fundamental organelle. Philos Trans R Soc Lond B Biol Sci. 2003;358:191–203. doi: 10.1098/rstb.2002.1190. [PMC free article] [PubMed] [Cross Ref]
  • Susko E, Roger AJ. On reduced amino acid alphabets for phylogenetic inference. Mol Biol Evol. 2007;24:2139–2150. doi: 10.1093/molbev/msm144. [PubMed] [Cross Ref]
  • Stuart A. A test for homogeneity of the marginal distributions in a two-way classification. Biometrika. 1955;42:412–416.
  • Ababneh F, Jermiin LS, Ma C, Robinson J. Matched-pairs tests of homogeneity with applications to homologous nucleotide sequences. Bioinformatics. 2006;22:1225–1231. doi: 10.1093/bioinformatics/btl064. [PubMed] [Cross Ref]
  • International Union of Pure and Applied Chemistery and International Union of Biochemistery (IUPAC-IUB) Commission on Biochemical Nomenclature. A one-letter notation for amino acid sequences (definitive rules) Pure Appl Chem. 1972;31:639–645. doi: 10.1351/pac197231040639. [Cross Ref]
  • Von Neumann J. Mathematische Grundlagen der Quantenmechanik. Berlin: Springer; 1932.
  • Caffrey DR, Somaroo S, Hughes JD, Mintseris J, Huang ES. Are protein-protein interfaces more conserved in sequence than the rest of the protein surface? Protein Sci. 2004;13:190–202. doi: 10.1110/ps.03323604. [PMC free article] [PubMed] [Cross Ref]
  • JAMA: A Java Matrix Package. http://math.nist.gov/javanumerics/jama/
  • Shannon C. A mathematical theory of communication. Bell System Tech J. 1948;27:379–423. 623-656.
  • Taylor WR. The classification of amino acid conservation. J Theor Biol. 1986;119:205–218. doi: 10.1016/S0022-5193(86)80075-3. [PubMed] [Cross Ref]
  • Bordo D, Argos P. Suggestion for "safe" residue substitutions in site-directed mutagenesis. J mol Biol. 1991;217:721–729. doi: 10.1016/0022-2836(91)90528-E. [PubMed] [Cross Ref]
  • Henikoff S, Henikoff JG. Amino acid substitution matrices from protein blocks. Proc Natl Acad Sci. 1992;89:10915–10919. doi: 10.1073/pnas.89.22.10915. [PMC free article] [PubMed] [Cross Ref]
  • BLOSUM matrices. http://blocks.fhcrc.org/blocks/uploads/blosum/
  • Eddy SR. Where did the BLOSUM62 alignment score matrix come from? Nat Biotechnol. 2004;22:1035–1036. doi: 10.1038/nbt0804-1035. [PubMed] [Cross Ref]
  • States DJ, Gish W, Altschul SF. Improved sensitivity of nucleic acid database searches using application-specific scoring matrices. Methods: A Companion to Methods Enzymol. 1991;3:66–70. doi: 10.1016/S1046-2023(05)80165-3. [Cross Ref]
  • Uesaka H. Validity and applicability of several tests for comparing marginal distributions of a square table with ordered categories. Behaviormetrika. 1991;30:65–78. doi: 10.2333/bhmk.18.30_65. [Cross Ref]
  • Press WH, Teukolsky SA, Vetterling WT, Flannery BP. Numerical Recipes in C -- The Art of Scientific Computing. 2. Cambridge: Cambridge University Press; 1992.
  • Artificial datasets used in [48] http://www.atgc-montpellier.fr/phyml/datasets.php
  • Rambaut A, Grassly NC. Seq-Gen: an application for the Monte Carlo simulation of DNA sequence evolution along phylogenetic trees. Comput Appl Biosci. 1997;13:235–238. [PubMed]
  • Jones D, Taylor W, Thornton J. The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci. 1992;8:275–282. [PubMed]
  • Guindon S, Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003;52:696–704. doi: 10.1080/10635150390235520. [PubMed] [Cross Ref]
  • Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32:1792–1797. doi: 10.1093/nar/gkh340. [PMC free article] [PubMed] [Cross Ref]
  • Edgar RC. MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics. 2004;5:113. doi: 10.1186/1471-2105-5-113. [PMC free article] [PubMed] [Cross Ref]
  • Egan JP. Signal detection theory and ROC analysis, series in cognition and perception. New York: Academic Press; 1975.
  • Metz CE. Basic principles of ROC analysis. Semin Nucl Med. 1978;8:283–298. doi: 10.1016/S0001-2998(78)80014-2. [PubMed] [Cross Ref]
  • Swets J. Measuring the accuracy of diagnostic systems. Science. 1988;240:1285–1293. doi: 10.1126/science.3287615. [PubMed] [Cross Ref]
  • Fawcett T. An introduction to ROC analysis. Pattern Recogn Lett. 2006;27:861–874. doi: 10.1016/j.patrec.2005.10.010. [Cross Ref]
  • McStewart W. A note on the power of the sign test. Ann Math Stat. 1941;12:279–303. doi: 10.1214/aoms/1177731710. [Cross Ref]
  • Dixon WJ, Mood AM. The statistical sign test. J Am Statist Assoc. 1946;41:557–566. doi: 10.2307/2280577. [PubMed] [Cross Ref]
  • Hemelrijk J. A theorem on the sign test when ties are present. Proc Nederl Akad Weten Ser A. 1952;55:322.
  • Gascuel O. BIONJ: an improved version of the NJ algorithm based on a simple model of sequence data. Mol Biol Evol. 1997;14:685–695. [PubMed]
  • Goloboff P, Farris S, Nixon KC. TNT (Tree analysis using New Technology) ver. 1.0. Published by the authors, Tucumán, Argentina; 2000.
  • Nixon KC. The parsimony ratchet, a new method for rapid parsimony analysis. Cladistics. 1999;15:407–414. doi: 10.1111/j.1096-0031.1999.tb00277.x. [Cross Ref]
  • Estabrook GF, McMorris FR, Meacham CA. Comparison of undirected phylogenetic trees based on subtrees of four evolutionary units. Syst Zool. 1985;34:193–200. doi: 10.2307/2413326. [Cross Ref]
  • Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 1985;39:783–791. doi: 10.2307/2408678. [Cross Ref]
  • Anisimova M, Gascuel O. Approximate likelihood ratio test for branches: a fast, accurate and powerful alternative. Syst Biol. 2006;55:539–552. doi: 10.1080/10635150600755453. [PubMed] [Cross Ref]
  • Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010;59:307–321. doi: 10.1093/sysbio/syq010. [PubMed] [Cross Ref]
  • Hanley JA, McNeil BJ. The meaning and the use of the area under a receiver operating characteristic (ROC) curve. Radiology. 1982;143:29–36. [PubMed]
  • Fogarty J, Baker RS, Hudson SE. In: Proceedings of Graphics Interface (GI 2005): 09-11 May 2005; Victoria, British Columbia. Michael McCool, editor. University of Waterloo; 2005. Case studies in the use of ROC curve analysis for sensor-based estimates in human computer interaction; pp. 129–136.
  • Concatenate: a software to build supermatrices of characters. http://www.supertriplets.univ-montp2.fr/PhyloTools.php
  • Adachi J, Hasegawa M. Model of amino acid substitution in proteins encoded by mitochondrial DNA. J Mol Evol. 1996;42:459–468. doi: 10.1007/BF02498640. [PubMed] [Cross Ref]
  • Rodríguez-Ezpeleta N, Brinkmann H, Burey SC, Roure B, Burger G, Löffelhardt W, Bohnert HJ, Philippe H. Monophyly of Primary Photosynthetic Eukaryotes: Green Plants, Red Algae, and Glaucophytes. Curr Biol. 2005;15:1325–1330. doi: 10.1016/j.cub.2005.06.040. [PubMed] [Cross Ref]
  • Hackett JD, Yoon HS, Li S, Reyes-Prieto A, Rümmele SE, Bhattacharya D. Phylogenomic analysis supports the monophyly of Cryptophytes and Haptophytes and the association of Rhizaria with Chromalveolates. Mol Biol Evol. 2007;24:1702–1713. doi: 10.1093/molbev/msm089. [PubMed] [Cross Ref]
  • Burki F, Shalchian-Tabrizi K, Pawlowski J. Phylogenomics reveals a new 'metagroup' including most photosynthetic eukaryotes. Biol Lett. 2008;4:366–369. doi: 10.1098/rsbl.2008.0224. [PMC free article] [PubMed] [Cross Ref]
  • Hampl V, Hug L, Leigh JW, Dacks JB, Lang BF, Simpson AGB, Roger AJ. Phylogenomic analyses support the monophyly of Excavata and resolve relationships among eukaryotic "supergroups". Proc Natl Acad Sci USA. 2009;106:3859–3864. doi: 10.1073/pnas.0807880106. [PMC free article] [PubMed] [Cross Ref]
  • Ewens W, Grant G. Statistical methods in bioinformatics: an introduction. Second. New York: Springer; 2005.
  • Felsenstein J. Evolutionary tree from DNA sequences: a maximum likelihood approach. J Mol Evol. 1981;17:368–376. doi: 10.1007/BF01734359. [PubMed] [Cross Ref]
  • Rzhetsky A, Nei M. Tests of applicability of several substitution models for DNA sequence data. Mol Biol Evol. 1995;12:131–151. [PubMed]
  • Bowker AH. A test for symmetry in contingency tables. J Am Stat Assoc. 1948;43:572–574. doi: 10.2307/2280710. [PubMed] [Cross Ref]
  • Rokas A, Williams BL, King N, Carroll SB. Genome-scale approaches to resolving incongruence in molecular phylogenies. Nature. 2003;425:798–804. doi: 10.1038/nature02053. [PubMed] [Cross Ref]
  • Yeast multi-gene dataset. http://systbio.org/files/Ren_etal_Rokas2003data.txt
  • Lanave C, Preparata G, Saccone C, Serio G. A new method for calculating evolutionary substitution rates. J Mol Evol. 1984;20:86–93. doi: 10.1007/BF02101990. [PubMed] [Cross Ref]
  • Rodriguez R, Oliver JL, Marin A, Medina JR. The general stochastic model of nucleotide substitution. J Theor Biol. 1990;142:485–501. doi: 10.1016/S0022-5193(05)80104-3. [PubMed] [Cross Ref]
  • Yang Z. Estimating the pattern of nucleotide substitution. J Mol Evol. 1994;39:105–111. [PubMed]
  • Lake JA. Reconstructing evolutionary trees from DNA and protein sequences: paralinear distances. Proc Natl Acad Sci USA. 1994;91:1455–1459. doi: 10.1073/pnas.91.4.1455. [PMC free article] [PubMed] [Cross Ref]
  • Lockhart PJ, Steel MA, Hendy MD, Penny D. Recovering evolutionary trees under a more realistic model of sequence evolution. Mol Biol Evol. 1994;11:605–612. [PubMed]
  • Steel MA. Recovering a tree from the leaf colourations it generates under a Markov model. Appl Math Lett. 1994;7:19–23. doi: 10.1016/0893-9659(94)90024-8. [Cross Ref]
  • Taylor DJ, Piel WH. An assessment of accuracy, error, and conflict with support values from genome-scale phylogenetic data. Mol Biol Evol. 2004;21:1534–1537. doi: 10.1093/molbev/msh156. [PubMed] [Cross Ref]
  • Ren F, Tanaka H, Yang Z. An empirical examination of the utility of codon-substitution models in phylogeny reconstruction. Syst Biol. 2005;54:808–818. doi: 10.1080/10635150500354688. [PubMed] [Cross Ref]
  • Burleigh JG, Driskell AC, Sanderson MJ. Supertree bootstrapping methods for assessing phylogenetic variation among genes in genome-scale data sets. Syst Biol. 2006;55:426–440. doi: 10.1080/10635150500541722. [PubMed] [Cross Ref]
  • Ané C, Larget B, Baum DA, Smith SD, Rokas A. Bayesian estimation of concordance among gene trees. Mol Biol Evol. 2007;24:412–426. doi: 10.1093/molbev/msl170. [PubMed] [Cross Ref]
  • Criscuolo A, Michel CJ. Phylogenetic inference with weighted codon evolutionary distances. J Mol Evol. 2009;68:377–392. doi: 10.1007/s00239-009-9212-y. [PubMed] [Cross Ref]
  • Néron B, Ménager H, Maufrais C, Joly N, Maupetit J, Letort S, Carrere S, Tuffery P, Letondal C. Mobyle: a new full web bioinformatics framework. Bioinformatics. 2009;25:3005–3011. doi: 10.1093/bioinformatics/btp493. [PMC free article] [PubMed] [Cross Ref]

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