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Results: 16

Related Articles by Review for PubMed (Select 20175920)

1.

DraGnET: software for storing, managing and analyzing annotated draft genome sequence data.

Duncan S, Sirkanungo R, Miller L, Phillips GJ.

BMC Bioinformatics. 2010 Feb 22;11:100. doi: 10.1186/1471-2105-11-100.

2.

The Genome Sequencer FLX System--longer reads, more applications, straight forward bioinformatics and more complete data sets.

Droege M, Hill B.

J Biotechnol. 2008 Aug 31;136(1-2):3-10. doi: 10.1016/j.jbiotec.2008.03.021. Epub 2008 Jun 21. Review.

PMID:
18616967
3.

Automated querying of genome databases.

Schattner P.

PLoS Comput Biol. 2007 Jan 26;3(1):e1. Review. No abstract available.

4.

UCSC genome browser: deep support for molecular biomedical research.

Mangan ME, Williams JM, Lathe SM, Karolchik D, Lathe WC 3rd.

Biotechnol Annu Rev. 2008;14:63-108. doi: 10.1016/S1387-2656(08)00003-3. Review.

PMID:
18606360
5.

Advances in the Exon-Intron Database (EID).

Shepelev V, Fedorov A.

Brief Bioinform. 2006 Jun;7(2):178-85. Epub 2006 Mar 9. Review.

6.

Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing.

Dolled-Filhart MP, Lee M Jr, Ou-Yang CW, Haraksingh RR, Lin JC.

ScientificWorldJournal. 2013;2013:730210. doi: 10.1155/2013/730210. Epub 2013 Jan 13. Review.

7.

Visualization techniques for genomic data.

Loraine AE, Helt GA.

Proc IEEE Comput Soc Bioinform Conf. 2002;1:321-6. Review.

PMID:
15838148
8.

Sequencing and genome assembly using next-generation technologies.

Nagarajan N, Pop M.

Methods Mol Biol. 2010;673:1-17. doi: 10.1007/978-1-60761-842-3_1. Review.

PMID:
20835789
9.

Genome mapping statistics and bioinformatics.

Mychaleckyj JC.

Methods Mol Biol. 2007;404:461-88. doi: 10.1007/978-1-59745-530-5_22. Review.

PMID:
18450063
10.

An introduction to the informatics of "next-generation" sequencing.

Stein LD.

Curr Protoc Bioinformatics. 2011 Dec;Chapter 11:Unit 11.1.. doi: 10.1002/0471250953.bi1101s36. Review.

PMID:
22161566
11.

Bioinformatics tools and databases for analysis of next-generation sequence data.

Lee HC, Lai K, Lorenc MT, Imelfort M, Duran C, Edwards D.

Brief Funct Genomics. 2012 Jan;11(1):12-24. doi: 10.1093/bfgp/elr037. Epub 2011 Dec 19. Review.

PMID:
22184335
12.

Next-generation sequence assembly: four stages of data processing and computational challenges.

El-Metwally S, Hamza T, Zakaria M, Helmy M.

PLoS Comput Biol. 2013;9(12):e1003345. doi: 10.1371/journal.pcbi.1003345. Epub 2013 Dec 12. Review.

13.

[Bioinformatics and GenEnv database in biological risk management].

Romano Spica V, Santoni D, Paparini A, Giammanco GM, Canali A, Orsini M, Castrignanò T.

Ig Sanita Pubbl. 2004 Nov-Dec;60(6):401-20. Review. Italian.

PMID:
17206231
14.

To detect and analyze sequence repeats whatever be their origin.

Nicolas J.

Methods Mol Biol. 2012;859:69-90. doi: 10.1007/978-1-61779-603-6_4. Review.

PMID:
22367866
15.

The expanding scope of DNA sequencing.

Shendure J, Lieberman Aiden E.

Nat Biotechnol. 2012 Nov;30(11):1084-94. doi: 10.1038/nbt.2421. Epub 2012 Nov 8. Review.

16.

Analysing and interpreting DNA methylation data.

Bock C.

Nat Rev Genet. 2012 Oct;13(10):705-19. doi: 10.1038/nrg3273. Review.

PMID:
22986265
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