347 related articles for article (PubMed ID: 17138589)
1. Visualization of genomic aberrations using Affymetrix SNP arrays.
Müller A; Holzmann K; Kestler HA
Bioinformatics; 2007 Feb; 23(4):496-7. PubMed ID: 17138589
[TBL] [Abstract][Full Text] [Related]
2. SNP mining porcine ESTs with MAVIANT, a novel tool for SNP evaluation and annotation.
Panitz F; Stengaard H; Hornshøj H; Gorodkin J; Hedegaard J; Cirera S; Thomsen B; Madsen LB; Høj A; Vingborg RK; Zahn B; Wang X; Wang X; Wernersson R; Jørgensen CB; Scheibye-Knudsen K; Arvin T; Lumholdt S; Sawera M; Green T; Nielsen BJ; Havgaard JH; Brunak S; Fredholm M; Bendixen C
Bioinformatics; 2007 Jul; 23(13):i387-91. PubMed ID: 17646321
[TBL] [Abstract][Full Text] [Related]
3. VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles.
La Rosa P; Viara E; Hupé P; Pierron G; Liva S; Neuvial P; Brito I; Lair S; Servant N; Robine N; Manié E; Brennetot C; Janoueix-Lerosey I; Raynal V; Gruel N; Rouveirol C; Stransky N; Stern MH; Delattre O; Aurias A; Radvanyi F; Barillot E
Bioinformatics; 2006 Sep; 22(17):2066-73. PubMed ID: 16820431
[TBL] [Abstract][Full Text] [Related]
4. MSQT for choosing SNP assays from multiple DNA alignments.
Warthmann N; Fitz J; Weigel D
Bioinformatics; 2007 Oct; 23(20):2784-7. PubMed ID: 17785349
[TBL] [Abstract][Full Text] [Related]
5. IntegratedMap: a Web interface for integrating genetic map data.
Yang H; Wang H; Gingle AR
Bioinformatics; 2005 May; 21(9):2126-7. PubMed ID: 15657101
[TBL] [Abstract][Full Text] [Related]
6. Combo: a whole genome comparative browser.
Engels R; Yu T; Burge C; Mesirov JP; DeCaprio D; Galagan JE
Bioinformatics; 2006 Jul; 22(14):1782-3. PubMed ID: 16709588
[TBL] [Abstract][Full Text] [Related]
7. 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; 7():470. PubMed ID: 17062145
[TBL] [Abstract][Full Text] [Related]
8. ALOHOMORA: a tool for linkage analysis using 10K SNP array data.
Rüschendorf F; Nürnberg P
Bioinformatics; 2005 May; 21(9):2123-5. PubMed ID: 15647291
[TBL] [Abstract][Full Text] [Related]
9. 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; 22(14):e523-9. PubMed ID: 16873516
[TBL] [Abstract][Full Text] [Related]
10. SNP-PHAGE--High throughput SNP discovery pipeline.
Matukumalli LK; Grefenstette JJ; Hyten DL; Choi IY; Cregan PB; Van Tassell CP
BMC Bioinformatics; 2006 Oct; 7():468. PubMed ID: 17059604
[TBL] [Abstract][Full Text] [Related]
11. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.
Ting JC; Ye Y; Thomas GH; Ruczinski I; Pevsner J
BMC Bioinformatics; 2006 Jan; 7():25. PubMed ID: 16420694
[TBL] [Abstract][Full Text] [Related]
12. CGHAnalyzer: a stand-alone software package for cancer genome analysis using array-based DNA copy number data.
Margolin AA; Greshock J; Naylor TL; Mosse Y; Maris JM; Bignell G; Saeed AI; Quackenbush J; Weber BL
Bioinformatics; 2005 Aug; 21(15):3308-11. PubMed ID: 15905276
[TBL] [Abstract][Full Text] [Related]
13. AutoGRAPH: an interactive web server for automating and visualizing comparative genome maps.
Derrien T; André C; Galibert F; Hitte C
Bioinformatics; 2007 Feb; 23(4):498-9. PubMed ID: 17145741
[TBL] [Abstract][Full Text] [Related]
14. SNPNB: analyzing neighboring-nucleotide biases on single nucleotide polymorphisms (SNPs).
Zhang F; Zhao Z
Bioinformatics; 2005 May; 21(10):2517-9. PubMed ID: 15769840
[TBL] [Abstract][Full Text] [Related]
15. Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.
Di X; Matsuzaki H; Webster TA; Hubbell E; Liu G; Dong S; Bartell D; Huang J; Chiles R; Yang G; Shen MM; Kulp D; Kennedy GC; Mei R; Jones KW; Cawley S
Bioinformatics; 2005 May; 21(9):1958-63. PubMed ID: 15657097
[TBL] [Abstract][Full Text] [Related]
16. ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.
Rigaill G; Hupé P; Almeida A; La Rosa P; Meyniel JP; Decraene C; Barillot E
Bioinformatics; 2008 Mar; 24(6):768-74. PubMed ID: 18252739
[TBL] [Abstract][Full Text] [Related]
17. GenomeDiagram: a python package for the visualization of large-scale genomic data.
Pritchard L; White JA; Birch PR; Toth IK
Bioinformatics; 2006 Mar; 22(5):616-7. PubMed ID: 16377612
[TBL] [Abstract][Full Text] [Related]
18. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.
Karchin R; Diekhans M; Kelly L; Thomas DJ; Pieper U; Eswar N; Haussler D; Sali A
Bioinformatics; 2005 Jun; 21(12):2814-20. PubMed ID: 15827081
[TBL] [Abstract][Full Text] [Related]
19. Panta rhei (QAlign2): an open graphical environment for sequence analysis.
Sammeth M; Griebel T; Tille F; Stoye J
Bioinformatics; 2006 Apr; 22(7):889-90. PubMed ID: 16418234
[TBL] [Abstract][Full Text] [Related]
20. SEAN: SNP prediction and display program utilizing EST sequence clusters.
Huntley D; Baldo A; Johri S; Sergot M
Bioinformatics; 2006 Feb; 22(4):495-6. PubMed ID: 16357032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
