492 related articles for article (PubMed ID: 20482838)
1. Towards a comprehensive structural variation map of an individual human genome.
Pang AW; MacDonald JR; Pinto D; Wei J; Rafiq MA; Conrad DF; Park H; Hurles ME; Lee C; Venter JC; Kirkness EF; Levy S; Feuk L; Scherer SW
Genome Biol; 2010; 11(5):R52. PubMed ID: 20482838
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
[TBL] [Abstract][Full Text] [Related]
3. Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.
Waszak SM; Hasin Y; Zichner T; Olender T; Keydar I; Khen M; Stütz AM; Schlattl A; Lancet D; Korbel JO
PLoS Comput Biol; 2010 Nov; 6(11):e1000988. PubMed ID: 21085617
[TBL] [Abstract][Full Text] [Related]
4. The diploid genome sequence of an individual human.
Levy S; Sutton G; Ng PC; Feuk L; Halpern AL; Walenz BP; Axelrod N; Huang J; Kirkness EF; Denisov G; Lin Y; MacDonald JR; Pang AW; Shago M; Stockwell TB; Tsiamouri A; Bafna V; Bansal V; Kravitz SA; Busam DA; Beeson KY; McIntosh TC; Remington KA; Abril JF; Gill J; Borman J; Rogers YH; Frazier ME; Scherer SW; Strausberg RL; Venter JC
PLoS Biol; 2007 Sep; 5(10):e254. PubMed ID: 17803354
[TBL] [Abstract][Full Text] [Related]
5. Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.
Shen H; Li J; Zhang J; Xu C; Jiang Y; Wu Z; Zhao F; Liao L; Chen J; Lin Y; Tian Q; Papasian CJ; Deng HW
PLoS One; 2013; 8(4):e59494. PubMed ID: 23577066
[TBL] [Abstract][Full Text] [Related]
6. High-resolution structural variants catalogue in a large-scale whole genome sequenced bovine family cohort data.
Lee YL; Bosse M; Takeda H; Moreira GCM; Karim L; Druet T; Oget-Ebrad C; Coppieters W; Veerkamp RF; Groenen MAM; Georges M; Bouwman AC; Charlier C
BMC Genomics; 2023 May; 24(1):225. PubMed ID: 37127590
[TBL] [Abstract][Full Text] [Related]
7. [DNA polymorphisms].
Suehiro Y; Furuya T; Sasaki K; Hinota Y
Rinsho Byori; 2013 Nov; 61(11):1001-7. PubMed ID: 24450105
[TBL] [Abstract][Full Text] [Related]
8. KoVariome: Korean National Standard Reference Variome database of whole genomes with comprehensive SNV, indel, CNV, and SV analyses.
Kim J; Weber JA; Jho S; Jang J; Jun J; Cho YS; Kim HM; Kim H; Kim Y; Chung O; Kim CG; Lee H; Kim BC; Han K; Koh I; Chae KS; Lee S; Edwards JS; Bhak J
Sci Rep; 2018 Apr; 8(1):5677. PubMed ID: 29618732
[TBL] [Abstract][Full Text] [Related]
9. Comprehensive DNA copy number profile and BAC library construction of an Indian individual.
Chakrabarty S; D'Souza RR; Bellampalli R; Rotti H; Saadi AV; Gopinath PM; Acharya RV; Govindaraj P; Thangaraj K; Satyamoorthy K
Gene; 2012 Jun; 500(2):186-93. PubMed ID: 22465536
[TBL] [Abstract][Full Text] [Related]
10. Detection of copy number variation using SNP genotyping.
Cooper GM; Mefford HC
Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
[TBL] [Abstract][Full Text] [Related]
11. A highly annotated whole-genome sequence of a Korean individual.
Kim JI; Ju YS; Park H; Kim S; Lee S; Yi JH; Mudge J; Miller NA; Hong D; Bell CJ; Kim HS; Chung IS; Lee WC; Lee JS; Seo SH; Yun JY; Woo HN; Lee H; Suh D; Lee S; Kim HJ; Yavartanoo M; Kwak M; Zheng Y; Lee MK; Park H; Kim JY; Gokcumen O; Mills RE; Zaranek AW; Thakuria J; Wu X; Kim RW; Huntley JJ; Luo S; Schroth GP; Wu TD; Kim H; Yang KS; Park WY; Kim H; Church GM; Lee C; Kingsmore SF; Seo JS
Nature; 2009 Aug; 460(7258):1011-5. PubMed ID: 19587683
[TBL] [Abstract][Full Text] [Related]
12. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
Shaikh TH; Gai X; Perin JC; Glessner JT; Xie H; Murphy K; O'Hara R; Casalunovo T; Conlin LK; D'Arcy M; Frackelton EC; Geiger EA; Haldeman-Englert C; Imielinski M; Kim CE; Medne L; Annaiah K; Bradfield JP; Dabaghyan E; Eckert A; Onyiah CC; Ostapenko S; Otieno FG; Santa E; Shaner JL; Skraban R; Smith RM; Elia J; Goldmuntz E; Spinner NB; Zackai EH; Chiavacci RM; Grundmeier R; Rappaport EF; Grant SF; White PS; Hakonarson H
Genome Res; 2009 Sep; 19(9):1682-90. PubMed ID: 19592680
[TBL] [Abstract][Full Text] [Related]
13. CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.
Falque M; Jebreen K; Paux E; Knaak C; Mezmouk S; Martin OC
Genetics; 2020 Mar; 214(3):561-576. PubMed ID: 31882400
[TBL] [Abstract][Full Text] [Related]
14. Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.
Zhan B; Fadista J; Thomsen B; Hedegaard J; Panitz F; Bendixen C
BMC Genomics; 2011 Nov; 12():557. PubMed ID: 22082336
[TBL] [Abstract][Full Text] [Related]
15. Whole-genome sequencing and genetic variant analysis of a Quarter Horse mare.
Doan R; Cohen ND; Sawyer J; Ghaffari N; Johnson CD; Dindot SV
BMC Genomics; 2012 Feb; 13():78. PubMed ID: 22340285
[TBL] [Abstract][Full Text] [Related]
16. Strategies for the detection of copy number and other structural variants in the human genome.
Carson AR; Feuk L; Mohammed M; Scherer SW
Hum Genomics; 2006 Jun; 2(6):403-14. PubMed ID: 16848978
[TBL] [Abstract][Full Text] [Related]
17. Origins and functional impact of copy number variation in the human genome.
Conrad DF; Pinto D; Redon R; Feuk L; Gokcumen O; Zhang Y; Aerts J; Andrews TD; Barnes C; Campbell P; Fitzgerald T; Hu M; Ihm CH; Kristiansson K; Macarthur DG; Macdonald JR; Onyiah I; Pang AW; Robson S; Stirrups K; Valsesia A; Walter K; Wei J; ; Tyler-Smith C; Carter NP; Lee C; Scherer SW; Hurles ME
Nature; 2010 Apr; 464(7289):704-12. PubMed ID: 19812545
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
Haraksingh RR; Abyzov A; Urban AE
BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
[TBL] [Abstract][Full Text] [Related]
19. Sensitive and accurate detection of copy number variants using read depth of coverage.
Yoon S; Xuan Z; Makarov V; Ye K; Sebat J
Genome Res; 2009 Sep; 19(9):1586-92. PubMed ID: 19657104
[TBL] [Abstract][Full Text] [Related]
20. Current analysis platforms and methods for detecting copy number variation.
Li W; Olivier M
Physiol Genomics; 2013 Jan; 45(1):1-16. PubMed ID: 23132758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
