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.
125 related articles for article (PubMed ID: 19384415)
1. Genetic structures of copy number variants revealed by genotyping single sperm. Luo M; Cui X; Fredman D; Brookes AJ; Azaro MA; Greenawalt DM; Hu G; Wang HY; Tereshchenko IV; Lin Y; Shentu Y; Gao R; Shen L; Li H PLoS One; 2009; 4(4):e5236. PubMed ID: 19384415 [TBL] [Abstract][Full Text] [Related]
2. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle. Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735 [TBL] [Abstract][Full Text] [Related]
3. Haplotype phasing and inheritance of copy number variants in nuclear families. Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576 [TBL] [Abstract][Full Text] [Related]
4. Systematic assessment of copy number variant detection via genome-wide SNP genotyping. Cooper GM; Zerr T; Kidd JM; Eichler EE; Nickerson DA Nat Genet; 2008 Oct; 40(10):1199-203. PubMed ID: 18776910 [TBL] [Abstract][Full Text] [Related]
5. Integrated detection and population-genetic analysis of SNPs and copy number variation. McCarroll SA; Kuruvilla FG; Korn JM; Cawley S; Nemesh J; Wysoker A; Shapero MH; de Bakker PI; Maller JB; Kirby A; Elliott AL; Parkin M; Hubbell E; Webster T; Mei R; Veitch J; Collins PJ; Handsaker R; Lincoln S; Nizzari M; Blume J; Jones KW; Rava R; Daly MJ; Gabriel SB; Altshuler D Nat Genet; 2008 Oct; 40(10):1166-74. PubMed ID: 18776908 [TBL] [Abstract][Full Text] [Related]
6. A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation events. Kukita Y; Yahara K; Tahira T; Higasa K; Sonoda M; Yamamoto K; Kato K; Wake N; Hayashi K Am J Hum Genet; 2010 Jun; 86(6):918-28. PubMed ID: 20537301 [TBL] [Abstract][Full Text] [Related]
7. MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data. Kato M; Nakamura Y; Tsunoda T Bioinformatics; 2008 Jul; 24(14):1645-6. PubMed ID: 18492685 [TBL] [Abstract][Full Text] [Related]
8. Population-genetic nature of copy number variations in the human genome. Kato M; Kawaguchi T; Ishikawa S; Umeda T; Nakamichi R; Shapero MH; Jones KW; Nakamura Y; Aburatani H; Tsunoda T Hum Mol Genet; 2010 Mar; 19(5):761-73. PubMed ID: 19966329 [TBL] [Abstract][Full Text] [Related]
9. Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes. Shen F; Huang J; Fitch KR; Truong VB; Kirby A; Chen W; Zhang J; Liu G; McCarroll SA; Jones KW; Shapero MH BMC Genet; 2008 Mar; 9():27. PubMed ID: 18373861 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084 [TBL] [Abstract][Full Text] [Related]
12. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117 [TBL] [Abstract][Full Text] [Related]
13. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Korn JM; Kuruvilla FG; McCarroll SA; Wysoker A; Nemesh J; Cawley S; Hubbell E; Veitch J; Collins PJ; Darvishi K; Lee C; Nizzari MM; Gabriel SB; Purcell S; Daly MJ; Altshuler D Nat Genet; 2008 Oct; 40(10):1253-60. PubMed ID: 18776909 [TBL] [Abstract][Full Text] [Related]
14. An accurate method for quantifying and analyzing copy number variation in porcine KIT by an oligonucleotide ligation assay. Seo BY; Park EW; Ahn SJ; Lee SH; Kim JH; Im HT; Lee JH; Cho IC; Kong IK; Jeon JT BMC Genet; 2007 Nov; 8():81. PubMed ID: 18036219 [TBL] [Abstract][Full Text] [Related]
16. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533 [TBL] [Abstract][Full Text] [Related]
17. Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes. Wu YL; Savelli SL; Yang Y; Zhou B; Rovin BH; Birmingham DJ; Nagaraja HN; Hebert LA; Yu CY J Immunol; 2007 Sep; 179(5):3012-25. PubMed ID: 17709516 [TBL] [Abstract][Full Text] [Related]
18. CNV discovery using SNP genotyping arrays. Yau C; Holmes CC Cytogenet Genome Res; 2008; 123(1-4):307-12. PubMed ID: 19287169 [TBL] [Abstract][Full Text] [Related]
19. High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians. Matsuzaki H; Wang PH; Hu J; Rava R; Fu GK Genome Biol; 2009; 10(11):R125. PubMed ID: 19900272 [TBL] [Abstract][Full Text] [Related]
20. Identification of Copy Number Variants from SNP Arrays Using PennCNV. Fang L; Wang K Methods Mol Biol; 2018; 1833():1-28. PubMed ID: 30039360 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]