389 related articles for article (PubMed ID: 21787409)
1. Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
Bainbridge MN; Wang M; Wu Y; Newsham I; Muzny DM; Jefferies JL; Albert TJ; Burgess DL; Gibbs RA
Genome Biol; 2011 Jul; 12(7):R68. PubMed ID: 21787409
[TBL] [Abstract][Full Text] [Related]
2. The GENCODE exome: sequencing the complete human exome.
Coffey AJ; Kokocinski F; Calafato MS; Scott CE; Palta P; Drury E; Joyce CJ; Leproust EM; Harrow J; Hunt S; Lehesjoki AE; Turner DJ; Hubbard TJ; Palotie A
Eur J Hum Genet; 2011 Jul; 19(7):827-31. PubMed ID: 21364695
[TBL] [Abstract][Full Text] [Related]
3. A comparative analysis of exome capture.
Parla JS; Iossifov I; Grabill I; Spector MS; Kramer M; McCombie WR
Genome Biol; 2011 Sep; 12(9):R97. PubMed ID: 21958622
[TBL] [Abstract][Full Text] [Related]
4. Comparison of solution-based exome capture methods for next generation sequencing.
Sulonen AM; Ellonen P; Almusa H; Lepistö M; Eldfors S; Hannula S; Miettinen T; Tyynismaa H; Salo P; Heckman C; Joensuu H; Raivio T; Suomalainen A; Saarela J
Genome Biol; 2011 Sep; 12(9):R94. PubMed ID: 21955854
[TBL] [Abstract][Full Text] [Related]
5. Variant detection sensitivity and biases in whole genome and exome sequencing.
Meynert AM; Ansari M; FitzPatrick DR; Taylor MS
BMC Bioinformatics; 2014 Jul; 15(1):247. PubMed ID: 25038816
[TBL] [Abstract][Full Text] [Related]
6. High throughput exome coverage of clinically relevant cardiac genes.
Manase D; D'Alessandro LC; Manickaraj AK; Al Turki S; Hurles ME; Mital S
BMC Med Genomics; 2014 Dec; 7():67. PubMed ID: 25496018
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive comparison of three commercial human whole-exome capture platforms.
Asan ; Xu Y; Jiang H; Tyler-Smith C; Xue Y; Jiang T; Wang J; Wu M; Liu X; Tian G; Wang J; Wang J; Yang H; Zhang X
Genome Biol; 2011 Sep; 12(9):R95. PubMed ID: 21955857
[TBL] [Abstract][Full Text] [Related]
8. Whole human exome capture for high-throughput sequencing.
Kim DW; Nam SH; Kim RN; Choi SH; Park HS
Genome; 2010 Jul; 53(7):568-74. PubMed ID: 20616878
[TBL] [Abstract][Full Text] [Related]
9. New insights into the performance of human whole-exome capture platforms.
Meienberg J; Zerjavic K; Keller I; Okoniewski M; Patrignani A; Ludin K; Xu Z; Steinmann B; Carrel T; Röthlisberger B; Schlapbach R; Bruggmann R; Matyas G
Nucleic Acids Res; 2015 Jun; 43(11):e76. PubMed ID: 25820422
[TBL] [Abstract][Full Text] [Related]
10. An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia.
Dias C; Sincan M; Cherukuri PF; Rupps R; Huang Y; Briemberg H; Selby K; Mullikin JC; Markello TC; Adams DR; Gahl WA; Boerkoel CF
Hum Mutat; 2012 Apr; 33(4):614-26. PubMed ID: 22311686
[TBL] [Abstract][Full Text] [Related]
11. Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.
Ramos E; Levinson BT; Chasnoff S; Hughes A; Young AL; Thornton K; Li A; Vallania FL; Province M; Druley TE
BMC Genomics; 2012 Dec; 13():683. PubMed ID: 23216810
[TBL] [Abstract][Full Text] [Related]
12. Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.
Lelieveld SH; Spielmann M; Mundlos S; Veltman JA; Gilissen C
Hum Mutat; 2015 Aug; 36(8):815-22. PubMed ID: 25973577
[TBL] [Abstract][Full Text] [Related]
13. Exome sequencing: capture and sequencing of all human coding regions for disease gene discovery.
Priya RR; Rajasimha HK; Brooks MJ; Swaroop A
Methods Mol Biol; 2012; 884():335-51. PubMed ID: 22688718
[TBL] [Abstract][Full Text] [Related]
14. A flexible approach for highly multiplexed candidate gene targeted resequencing.
Natsoulis G; Bell JM; Xu H; Buenrostro JD; Ordonez H; Grimes S; Newburger D; Jensen M; Zahn JM; Zhang N; Ji HP
PLoS One; 2011; 6(6):e21088. PubMed ID: 21738606
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes.
Pruitt KD; Harrow J; Harte RA; Wallin C; Diekhans M; Maglott DR; Searle S; Farrell CM; Loveland JE; Ruef BJ; Hart E; Suner MM; Landrum MJ; Aken B; Ayling S; Baertsch R; Fernandez-Banet J; Cherry JL; Curwen V; Dicuccio M; Kellis M; Lee J; Lin MF; Schuster M; Shkeda A; Amid C; Brown G; Dukhanina O; Frankish A; Hart J; Maidak BL; Mudge J; Murphy MR; Murphy T; Rajan J; Rajput B; Riddick LD; Snow C; Steward C; Webb D; Weber JA; Wilming L; Wu W; Birney E; Haussler D; Hubbard T; Ostell J; Durbin R; Lipman D
Genome Res; 2009 Jul; 19(7):1316-23. PubMed ID: 19498102
[TBL] [Abstract][Full Text] [Related]
17. Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling.
Zhang G; Wang J; Yang J; Li W; Deng Y; Li J; Huang J; Hu S; Zhang B
BMC Genomics; 2015 Aug; 16(1):581. PubMed ID: 26242175
[TBL] [Abstract][Full Text] [Related]
18. Targeted analysis of nucleotide and copy number variation by exon capture in allotetraploid wheat genome.
Saintenac C; Jiang D; Akhunov ED
Genome Biol; 2011 Sep; 12(9):R88. PubMed ID: 21917144
[TBL] [Abstract][Full Text] [Related]
19. Design and application of a target capture sequencing of exons and conserved non-coding sequences for the rat.
Yoshihara M; Saito D; Sato T; Ohara O; Kuramoto T; Suyama M
BMC Genomics; 2016 Aug; 17():593. PubMed ID: 27506932
[TBL] [Abstract][Full Text] [Related]
20. The functional spectrum of low-frequency coding variation.
Marth GT; Yu F; Indap AR; Garimella K; Gravel S; Leong WF; Tyler-Smith C; Bainbridge M; Blackwell T; Zheng-Bradley X; Chen Y; Challis D; Clarke L; Ball EV; Cibulskis K; Cooper DN; Fulton B; Hartl C; Koboldt D; Muzny D; Smith R; Sougnez C; Stewart C; Ward A; Yu J; Xue Y; Altshuler D; Bustamante CD; Clark AG; Daly M; DePristo M; Flicek P; Gabriel S; Mardis E; Palotie A; Gibbs R;
Genome Biol; 2011 Sep; 12(9):R84. PubMed ID: 21917140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
