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Items: 1 to 20 of 96


SigCS base: an integrated genetic information resource for human cerebral stroke.

Park YK, Bang OS, Cha MH, Kim J, Cole JW, Lee D, Kim YJ.

BMC Syst Biol. 2011;5 Suppl 2:S10. doi: 10.1186/1752-0509-5-S2-S10. Epub 2011 Dec 14.


CGKB: an annotation knowledge base for cowpea (Vigna unguiculata L.) methylation filtered genomic genespace sequences.

Chen X, Laudeman TW, Rushton PJ, Spraggins TA, Timko MP.

BMC Bioinformatics. 2007 Apr 19;8:129.


An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.

Yang JO, Hwang S, Oh J, Bhak J, Sohn TK.

BMC Bioinformatics. 2008 Dec 12;9 Suppl 12:S19. doi: 10.1186/1471-2105-9-S12-S19.


WeGAS: a web-based microbial genome annotation system.

Lee D, Seo H, Park C, Park K.

Biosci Biotechnol Biochem. 2009 Jan;73(1):213-6. Epub 2009 Jan 7.


Rat Genome Database (RGD): mapping disease onto the genome.

Twigger S, Lu J, Shimoyama M, Chen D, Pasko D, Long H, Ginster J, Chen CF, Nigam R, Kwitek A, Eppig J, Maltais L, Maglott D, Schuler G, Jacob H, Tonellato PJ.

Nucleic Acids Res. 2002 Jan 1;30(1):125-8.


DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis.

Sherman BT, Huang da W, Tan Q, Guo Y, Bour S, Liu D, Stephens R, Baseler MW, Lane HC, Lempicki RA.

BMC Bioinformatics. 2007 Nov 2;8:426.


RASOnD-a comprehensive resource and search tool for RAS superfamily oncogenes from various species.

Kulsum U, Singh V, Sharma S, Srinivasan A, Singh TP, Kaur P.

BMC Genomics. 2011 Jul 5;12:341. doi: 10.1186/1471-2164-12-341.


GeneTools--application for functional annotation and statistical hypothesis testing.

Beisvag V, Jünge FK, Bergum H, Jølsum L, Lydersen S, Günther CC, Ramampiaro H, Langaas M, Sandvik AK, Laegreid A.

BMC Bioinformatics. 2006 Oct 24;7:470.


Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project.

Clifford R, Edmonson M, Hu Y, Nguyen C, Scherpbier T, Buetow KH.

Genome Res. 2000 Aug;10(8):1259-65.


GarlicESTdb: an online database and mining tool for garlic EST sequences.

Kim DW, Jung TS, Nam SH, Kwon HR, Kim A, Chae SH, Choi SH, Kim DW, Kim RN, Park HS.

BMC Plant Biol. 2009 May 18;9:61. doi: 10.1186/1471-2229-9-61.


BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

Moore CB, Wallace JR, Frase AT, Pendergrass SA, Ritchie MD.

BMC Med Genomics. 2013;6 Suppl 2:S6. doi: 10.1186/1755-8794-6-S2-S6. Epub 2013 May 7.


The Pain Genes Database: An interactive web browser of pain-related transgenic knockout studies.

Lacroix-Fralish ML, Ledoux JB, Mogil JS.

Pain. 2007 Sep;131(1-2):3.e1-4. Epub 2007 Jun 14. Review.


Non-coding sequence retrieval system for comparative genomic analysis of gene regulatory elements.

Doh ST, Zhang Y, Temple MH, Cai L.

BMC Bioinformatics. 2007 Mar 15;8:94.


SNP Function Portal: a web database for exploring the function implication of SNP alleles.

Wang P, Dai M, Xuan W, McEachin RC, Jackson AU, Scott LJ, Athey B, Watson SJ, Meng F.

Bioinformatics. 2006 Jul 15;22(14):e523-9.


SNP2NMD: a database of human single nucleotide polymorphisms causing nonsense-mediated mRNA decay.

Han A, Kim WY, Park SM.

Bioinformatics. 2007 Feb 1;23(3):397-9. Epub 2006 Nov 22.


HOWDY: an integrated database system for human genome research.

Hirakawa M.

Nucleic Acids Res. 2002 Jan 1;30(1):152-7.


Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline.

Lee IH, Lee K, Hsing M, Choe Y, Park JH, Kim SH, Bohn JM, Neu MB, Hwang KB, Green RC, Kohane IS, Kong SW.

Hum Mutat. 2014 May;35(5):537-47. doi: 10.1002/humu.22520. Epub 2014 Mar 6.


SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes.

Packer BR, Yeager M, Staats B, Welch R, Crenshaw A, Kiley M, Eckert A, Beerman M, Miller E, Bergen A, Rothman N, Strausberg R, Chanock SJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D528-32.

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