These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
127 related articles for article (PubMed ID: 22289434)
21. Exome-wide DNA capture and next generation sequencing in domestic and wild species. Cosart T; Beja-Pereira A; Chen S; Ng SB; Shendure J; Luikart G BMC Genomics; 2011 Jul; 12():347. PubMed ID: 21729323 [TBL] [Abstract][Full Text] [Related]
22. Weighted single-step genomic best linear unbiased prediction integrating variants selected from sequencing data by association and bioinformatics analyses. Liu A; Lund MS; Boichard D; Karaman E; Guldbrandtsen B; Fritz S; Aamand GP; Nielsen US; Sahana G; Wang Y; Su G Genet Sel Evol; 2020 Aug; 52(1):48. PubMed ID: 32799816 [TBL] [Abstract][Full Text] [Related]
23. Combining SNP discovery from next-generation sequencing data with bulked segregant analysis (BSA) to fine-map genes in polyploid wheat. Trick M; Adamski NM; Mugford SG; Jiang CC; Febrer M; Uauy C BMC Plant Biol; 2012 Jan; 12():14. PubMed ID: 22280551 [TBL] [Abstract][Full Text] [Related]
24. Integrating pathway analysis and genetics of gene expression for genome-wide association studies. Zhong H; Yang X; Kaplan LM; Molony C; Schadt EE Am J Hum Genet; 2010 Apr; 86(4):581-91. PubMed ID: 20346437 [TBL] [Abstract][Full Text] [Related]
25. A beginners guide to SNP calling from high-throughput DNA-sequencing data. Altmann A; Weber P; Bader D; Preuss M; Binder EB; Müller-Myhsok B Hum Genet; 2012 Oct; 131(10):1541-54. PubMed ID: 22886560 [TBL] [Abstract][Full Text] [Related]
26. Assessing statistical significance in multivariable genome wide association analysis. Buzdugan L; Kalisch M; Navarro A; Schunk D; Fehr E; Bühlmann P Bioinformatics; 2016 Jul; 32(13):1990-2000. PubMed ID: 27153677 [TBL] [Abstract][Full Text] [Related]
27. 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Huang J; Ellinghaus D; Franke A; Howie B; Li Y Eur J Hum Genet; 2012 Jul; 20(7):801-5. PubMed ID: 22293688 [TBL] [Abstract][Full Text] [Related]
28. SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS. Merelli I; Calabria A; Cozzi P; Viti F; Mosca E; Milanesi L BMC Bioinformatics; 2013; 14 Suppl 1(Suppl 1):S9. PubMed ID: 23369106 [TBL] [Abstract][Full Text] [Related]
29. Targeted single nucleotide polymorphism (SNP) discovery in a highly polyploid plant species using 454 sequencing. Bundock PC; Eliott FG; Ablett G; Benson AD; Casu RE; Aitken KS; Henry RJ Plant Biotechnol J; 2009 May; 7(4):347-54. PubMed ID: 19386042 [TBL] [Abstract][Full Text] [Related]
30. A method for discovery of genome-wide SNP between any two genotypes from whole-genome re-sequencing data. Krishnan SG; Waters DL; Henry RJ Methods Mol Biol; 2014; 1099():287-94. PubMed ID: 24243213 [TBL] [Abstract][Full Text] [Related]
31. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]. Zhang DL; Ji L; Li YD Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601 [TBL] [Abstract][Full Text] [Related]
32. Global inference of disease-causing single nucleotide variants from exome sequencing data. Wu M; Chen T; Jiang R BMC Bioinformatics; 2016 Dec; 17(Suppl 17):468. PubMed ID: 28155632 [TBL] [Abstract][Full Text] [Related]
33. Functional annotation of sixty-five type-2 diabetes risk SNPs and its application in risk prediction. Wu Y; Jing R; Dong Y; Kuang Q; Li Y; Huang Z; Gan W; Xue Y; Li Y; Li M Sci Rep; 2017 Mar; 7():43709. PubMed ID: 28262806 [TBL] [Abstract][Full Text] [Related]
34. SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries. Van Tassell CP; Smith TP; Matukumalli LK; Taylor JF; Schnabel RD; Lawley CT; Haudenschild CD; Moore SS; Warren WC; Sonstegard TS Nat Methods; 2008 Mar; 5(3):247-52. PubMed ID: 18297082 [TBL] [Abstract][Full Text] [Related]
35. Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design. Field HI; Scollen SA; Luccarini C; Baynes C; Morrison J; Dunning AM; Easton DF; Pharoah PD BMC Bioinformatics; 2009 Jun; 10():180. PubMed ID: 19523221 [TBL] [Abstract][Full Text] [Related]
36. Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology. Oliver RE; Lazo GR; Lutz JD; Rubenfield MJ; Tinker NA; Anderson JM; Wisniewski Morehead NH; Adhikary D; Jellen EN; Maughan PJ; Brown Guedira GL; Chao S; Beattie AD; Carson ML; Rines HW; Obert DE; Bonman JM; Jackson EW BMC Genomics; 2011 Jan; 12():77. PubMed ID: 21272354 [TBL] [Abstract][Full Text] [Related]
37. Prediction of disease-associated single nucleotide polymorphisms using virtual genomes constructed from a public haplotype database. Toyabe S; Miyashita A; Kitamura N; Kuwano R; Akazawa K Methods Inf Med; 2008; 47(6):522-8. PubMed ID: 19057809 [TBL] [Abstract][Full Text] [Related]
38. The sequence of the human genome. Venter JC; Adams MD; Myers EW; Li PW; Mural RJ; Sutton GG; Smith HO; Yandell M; Evans CA; Holt RA; Gocayne JD; Amanatides P; Ballew RM; Huson DH; Wortman JR; Zhang Q; Kodira CD; Zheng XH; Chen L; Skupski M; Subramanian G; Thomas PD; Zhang J; Gabor Miklos GL; Nelson C; Broder S; Clark AG; Nadeau J; McKusick VA; Zinder N; Levine AJ; Roberts RJ; Simon M; Slayman C; Hunkapiller M; Bolanos R; Delcher A; Dew I; Fasulo D; Flanigan M; Florea L; Halpern A; Hannenhalli S; Kravitz S; Levy S; Mobarry C; Reinert K; Remington K; Abu-Threideh J; Beasley E; Biddick K; Bonazzi V; Brandon R; Cargill M; Chandramouliswaran I; Charlab R; Chaturvedi K; Deng Z; Di Francesco V; Dunn P; Eilbeck K; Evangelista C; Gabrielian AE; Gan W; Ge W; Gong F; Gu Z; Guan P; Heiman TJ; Higgins ME; Ji RR; Ke Z; Ketchum KA; Lai Z; Lei Y; Li Z; Li J; Liang Y; Lin X; Lu F; Merkulov GV; Milshina N; Moore HM; Naik AK; Narayan VA; Neelam B; Nusskern D; Rusch DB; Salzberg S; Shao W; Shue B; Sun J; Wang Z; Wang A; Wang X; Wang J; Wei M; Wides R; Xiao C; Yan C; Yao A; Ye J; Zhan M; Zhang W; Zhang H; Zhao Q; Zheng L; Zhong F; Zhong W; Zhu S; Zhao S; Gilbert D; Baumhueter S; Spier G; Carter C; Cravchik A; Woodage T; Ali F; An H; Awe A; Baldwin D; Baden H; Barnstead M; Barrow I; Beeson K; Busam D; Carver A; Center A; Cheng ML; Curry L; Danaher S; Davenport L; Desilets R; Dietz S; Dodson K; Doup L; Ferriera S; Garg N; Gluecksmann A; Hart B; Haynes J; Haynes C; Heiner C; Hladun S; Hostin D; Houck J; Howland T; Ibegwam C; Johnson J; Kalush F; Kline L; Koduru S; Love A; Mann F; May D; McCawley S; McIntosh T; McMullen I; Moy M; Moy L; Murphy B; Nelson K; Pfannkoch C; Pratts E; Puri V; Qureshi H; Reardon M; Rodriguez R; Rogers YH; Romblad D; Ruhfel B; Scott R; Sitter C; Smallwood M; Stewart E; Strong R; Suh E; Thomas R; Tint NN; Tse S; Vech C; Wang G; Wetter J; Williams S; Williams M; Windsor S; Winn-Deen E; Wolfe K; Zaveri J; Zaveri K; Abril JF; Guigó R; Campbell MJ; Sjolander KV; Karlak B; Kejariwal A; Mi H; Lazareva B; Hatton T; Narechania A; Diemer K; Muruganujan A; Guo N; Sato S; Bafna V; Istrail S; Lippert R; Schwartz R; Walenz B; Yooseph S; Allen D; Basu A; Baxendale J; Blick L; Caminha M; Carnes-Stine J; Caulk P; Chiang YH; Coyne M; Dahlke C; Deslattes Mays A; Dombroski M; Donnelly M; Ely D; Esparham S; Fosler C; Gire H; Glanowski S; Glasser K; Glodek A; Gorokhov M; Graham K; Gropman B; Harris M; Heil J; Henderson S; Hoover J; Jennings D; Jordan C; Jordan J; Kasha J; Kagan L; Kraft C; Levitsky A; Lewis M; Liu X; Lopez J; Ma D; Majoros W; McDaniel J; Murphy S; Newman M; Nguyen T; Nguyen N; Nodell M; Pan S; Peck J; Peterson M; Rowe W; Sanders R; Scott J; Simpson M; Smith T; Sprague A; Stockwell T; Turner R; Venter E; Wang M; Wen M; Wu D; Wu M; Xia A; Zandieh A; Zhu X Science; 2001 Feb; 291(5507):1304-51. PubMed ID: 11181995 [TBL] [Abstract][Full Text] [Related]
39. Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. Uimari O; Rahmioglu N; Nyholt DR; Vincent K; Missmer SA; Becker C; Morris AP; Montgomery GW; Zondervan KT Hum Reprod; 2017 Apr; 32(4):780-793. PubMed ID: 28333195 [TBL] [Abstract][Full Text] [Related]
40. Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases. Cavalli M; Baltzer N; Pan G; Bárcenas Walls JR; Smolinska Garbulowska K; Kumar C; Skrtic S; Komorowski J; Wadelius C Hum Genomics; 2019 Apr; 13(1):20. PubMed ID: 31036066 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]