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Nucleic Acids Res. 2014 Jul;42(12):e99. doi: 10.1093/nar/gku356. Epub 2014 May 6.

Realistic artificial DNA sequences as negative controls for computational genomics.

Author information

1
Institute for Systems Biology, 401 Terry Ave. N, Seattle, WA 98109, USA.
2
Institute for Systems Biology, 401 Terry Ave. N, Seattle, WA 98109, USA gustavo@systemsbiology.org.

Abstract

A common practice in computational genomic analysis is to use a set of 'background' sequences as negative controls for evaluating the false-positive rates of prediction tools, such as gene identification programs and algorithms for detection of cis-regulatory elements. Such 'background' sequences are generally taken from regions of the genome presumed to be intergenic, or generated synthetically by 'shuffling' real sequences. This last method can lead to underestimation of false-positive rates. We developed a new method for generating artificial sequences that are modeled after real intergenic sequences in terms of composition, complexity and interspersed repeat content. These artificial sequences can serve as an inexhaustible source of high-quality negative controls. We used artificial sequences to evaluate the false-positive rates of a set of programs for detecting interspersed repeats, ab initio prediction of coding genes, transcribed regions and non-coding genes. We found that RepeatMasker is more accurate than PClouds, Augustus has the lowest false-positive rate of the coding gene prediction programs tested, and Infernal has a low false-positive rate for non-coding gene detection. A web service, source code and the models for human and many other species are freely available at http://repeatmasker.org/garlic/.

PMID:
24803667
PMCID:
PMC4081056
DOI:
10.1093/nar/gku356
[Indexed for MEDLINE]
Free PMC Article

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