205 related articles for article (PubMed ID: 21179565)
1. Microarray-based maps of copy-number variant regions in European and sub-Saharan populations.
Vogler C; Gschwind L; Röthlisberger B; Huber A; Filges I; Miny P; Auschra B; Stetak A; Demougin P; Vukojevic V; Kolassa IT; Elbert T; de Quervain DJ; Papassotiropoulos A
PLoS One; 2010 Dec; 5(12):e15246. PubMed ID: 21179565
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide identification of copy number variation using high-density single-nucleotide polymorphism array in Japanese Black cattle.
Sasaki S; Watanabe T; Nishimura S; Sugimoto Y
BMC Genet; 2016 Jan; 17():26. PubMed ID: 26809925
[TBL] [Abstract][Full Text] [Related]
3. Copy number variants in the sheep genome detected using multiple approaches.
Jenkins GM; Goddard ME; Black MA; Brauning R; Auvray B; Dodds KG; Kijas JW; Cockett N; McEwan JC
BMC Genomics; 2016 Jun; 17():441. PubMed ID: 27277319
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Analysis of copy number variations in the sheep genome using 50K SNP BeadChip array.
Liu J; Zhang L; Xu L; Ren H; Lu J; Zhang X; Zhang S; Zhou X; Wei C; Zhao F; Du L
BMC Genomics; 2013 Apr; 14():229. PubMed ID: 23565757
[TBL] [Abstract][Full Text] [Related]
6. CNV analysis in the Lithuanian population.
Urnikyte A; Domarkiene I; Stoma S; Ambrozaityte L; Uktveryte I; Meskiene R; Kasiulevičius V; Burokiene N; Kučinskas V
BMC Genet; 2016 May; 17(1):64. PubMed ID: 27142071
[TBL] [Abstract][Full Text] [Related]
7. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
[TBL] [Abstract][Full Text] [Related]
8. Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array.
Ma Q; Liu X; Pan J; Ma L; Ma Y; He X; Zhao Q; Pu Y; Li Y; Jiang L
Sci Rep; 2017 Apr; 7(1):912. PubMed ID: 28424525
[TBL] [Abstract][Full Text] [Related]
9. Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
Eckel-Passow JE; Atkinson EJ; Maharjan S; Kardia SL; de Andrade M
BMC Bioinformatics; 2011 May; 12():220. PubMed ID: 21627824
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.
Salomón-Torres R; González-Vizcarra VM; Medina-Basulto GE; Montaño-Gómez MF; Mahadevan P; Yaurima-Basaldúa VH; Villa-Angulo C; Villa-Angulo R
Genet Mol Res; 2015 Oct; 14(4):11848-59. PubMed ID: 26436509
[TBL] [Abstract][Full Text] [Related]
11. A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH data.
Park C; Ahn J; Yoon Y; Park S
PLoS One; 2011; 6(10):e26975. PubMed ID: 22073121
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide copy number profiling using high-density SNP array in chickens.
Yi G; Qu L; Chen S; Xu G; Yang N
Anim Genet; 2015 Apr; 46(2):148-57. PubMed ID: 25662183
[TBL] [Abstract][Full Text] [Related]
13. Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array.
Hou Y; Bickhart DM; Hvinden ML; Li C; Song J; Boichard DA; Fritz S; Eggen A; DeNise S; Wiggans GR; Sonstegard TS; Van Tassell CP; Liu GE
BMC Genomics; 2012 Aug; 13():376. PubMed ID: 22866901
[TBL] [Abstract][Full Text] [Related]
14. The effect of algorithms on copy number variant detection.
Tsuang DW; Millard SP; Ely B; Chi P; Wang K; Raskind WH; Kim S; Brkanac Z; Yu CE
PLoS One; 2010 Dec; 5(12):e14456. PubMed ID: 21209939
[TBL] [Abstract][Full Text] [Related]
15. Detection and analysis of genome-wide copy number variation in the pig genome using an 80 K SNP Beadchip.
Wang Y; Zhang T; Wang C
J Anim Breed Genet; 2020 Mar; 137(2):166-176. PubMed ID: 31506991
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Analysis of copy number variation in dogs implicates genomic structural variation in the development of anterior cruciate ligament rupture.
Binversie EE; Baker LA; Engelman CD; Hao Z; Moran JJ; Piazza AM; Sample SJ; Muir P
PLoS One; 2020; 15(12):e0244075. PubMed ID: 33382735
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide elucidation of CNV regions and their association with production and reproduction traits in composite Vrindavani cattle.
Ahmad SF; Singh A; Panda S; Malla WA; Kumar A; Dutt T
Gene; 2022 Jul; 830():146510. PubMed ID: 35447249
[TBL] [Abstract][Full Text] [Related]
19. Copy number variations (CNVs) identified in Korean individuals.
Kang TW; Jeon YJ; Jang E; Kim HJ; Kim JH; Park JL; Lee S; Kim YS; Kim JY; Kim SY
BMC Genomics; 2008 Oct; 9():492. PubMed ID: 18928558
[TBL] [Abstract][Full Text] [Related]
20. Copy number variations in the genome of the Qatari population.
Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]