85 related articles for article (PubMed ID: 30039362)
1. Statistical Detection of Genome Differences Based on CNV Segments.
Zhou Y; Bickhart DM; Liu GE
Methods Mol Biol; 2018; 1833():49-59. PubMed ID: 30039362
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Detection of copy number variations in brown and white layers based on genotyping panels with different densities.
Drobik-Czwarno W; Wolc A; Fulton JE; Dekkers JCM
Genet Sel Evol; 2018 Nov; 50(1):54. PubMed ID: 30400769
[TBL] [Abstract][Full Text] [Related]
5. Family-Based Benchmarking of Copy Number Variation Detection Software.
Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
[TBL] [Abstract][Full Text] [Related]
6. On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.
Ionita-Laza I; Perry GH; Raby BA; Klanderman B; Lee C; Laird NM; Weiss ST; Lange C
Genet Epidemiol; 2008 Apr; 32(3):273-84. PubMed ID: 18228561
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
[TBL] [Abstract][Full Text] [Related]
8. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
[TBL] [Abstract][Full Text] [Related]
9. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Wang K; Li M; Hadley D; Liu R; Glessner J; Grant SF; Hakonarson H; Bucan M
Genome Res; 2007 Nov; 17(11):1665-74. PubMed ID: 17921354
[TBL] [Abstract][Full Text] [Related]
10. A novel scatterplot-based method to detect copy number variation (CNV).
Qiao JL; Levinson RT; Chen B; Engelter ST; Erhart P; Gaynor BJ; McArdle PF; Schlicht K; Krawczak M; Stenman M; Lindgren AG; Cole JW; Grond-Ginsbach C
Front Genet; 2023; 14():1166972. PubMed ID: 37485343
[No Abstract] [Full Text] [Related]
11. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
12. An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.
Zare F; Dow M; Monteleone N; Hosny A; Nabavi S
BMC Bioinformatics; 2017 May; 18(1):286. PubMed ID: 28569140
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.
Castellani CA; Melka MG; Wishart AE; Locke ME; Awamleh Z; O'Reilly RL; Singh SM
BMC Bioinformatics; 2014 Apr; 15():114. PubMed ID: 24750645
[TBL] [Abstract][Full Text] [Related]
15. A robust statistical method for case-control association testing with copy number variation.
Barnes C; Plagnol V; Fitzgerald T; Redon R; Marchini J; Clayton D; Hurles ME
Nat Genet; 2008 Oct; 40(10):1245-52. PubMed ID: 18776912
[TBL] [Abstract][Full Text] [Related]
16. Copy number polymorphisms and anticancer pharmacogenomics.
Gamazon ER; Huang RS; Dolan ME; Cox NJ
Genome Biol; 2011; 12(5):R46. PubMed ID: 21609475
[TBL] [Abstract][Full Text] [Related]
17. New quality measure for SNP array based CNV detection.
Macé A; Tuke MA; Beckmann JS; Lin L; Jacquemont S; Weedon MN; Reymond A; Kutalik Z
Bioinformatics; 2016 Nov; 32(21):3298-3305. PubMed ID: 27402902
[TBL] [Abstract][Full Text] [Related]
18. Global variation in copy number in the human genome.
Redon R; Ishikawa S; Fitch KR; Feuk L; Perry GH; Andrews TD; Fiegler H; Shapero MH; Carson AR; Chen W; Cho EK; Dallaire S; Freeman JL; González JR; Gratacòs M; Huang J; Kalaitzopoulos D; Komura D; MacDonald JR; Marshall CR; Mei R; Montgomery L; Nishimura K; Okamura K; Shen F; Somerville MJ; Tchinda J; Valsesia A; Woodwark C; Yang F; Zhang J; Zerjal T; Zhang J; Armengol L; Conrad DF; Estivill X; Tyler-Smith C; Carter NP; Aburatani H; Lee C; Jones KW; Scherer SW; Hurles ME
Nature; 2006 Nov; 444(7118):444-54. PubMed ID: 17122850
[TBL] [Abstract][Full Text] [Related]
19. Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.
Bae JS; Cheong HS; Kim JO; Lee SO; Kim EM; Lee HW; Kim S; Kim JW; Cui T; Inoue I; Shin HD
Biochem Biophys Res Commun; 2008 Sep; 373(4):593-6. PubMed ID: 18601904
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]