273 related articles for article (PubMed ID: 22734463)
1. Cheek swabs, SNP chips, and CNVs: assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray.
Erickson SW; MacLeod SL; Hobbs CA
BMC Med Genet; 2012 Jun; 13():51. PubMed ID: 22734463
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide algorithm for detecting CNV associations with diseases.
Xu Y; Peng B; Fu Y; Amos CI
BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.
Shrine N; Tobin MD; Schurmann C; Soler Artigas M; Hui J; Lehtimäki T; Raitakari OT; Pennell CE; Ang QW; Strachan DP; Homuth G; Gläser S; Felix SB; Evans DM; Henderson J; Granell R; Palmer LJ; Huffman J; Hayward C; Scotland G; Malarstig A; Musk B; James AL; ; Wain LV
BMC Genet; 2016 Aug; 17(1):116. PubMed ID: 27514831
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. CNV Concordance in 1,097 MZ Twin Pairs.
Abdellaoui A; Ehli EA; Hottenga JJ; Weber Z; Mbarek H; Willemsen G; van Beijsterveldt T; Brooks A; Hudziak JJ; Sullivan PF; de Geus EJ; Davies GE; Boomsma DI
Twin Res Hum Genet; 2015 Feb; 18(1):1-12. PubMed ID: 25578775
[TBL] [Abstract][Full Text] [Related]
8. Fast detection of de novo copy number variants from SNP arrays for case-parent trios.
Scharpf RB; Beaty TH; Schwender H; Younkin SG; Scott AF; Ruczinski I
BMC Bioinformatics; 2012 Dec; 13():330. PubMed ID: 23234608
[TBL] [Abstract][Full Text] [Related]
9. Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies.
Zheng X; Shaffer JR; McHugh CP; Laurie CC; Feenstra B; Melbye M; Murray JC; Marazita ML; Feingold E
Genet Epidemiol; 2012 Apr; 36(3):253-62. PubMed ID: 22714937
[TBL] [Abstract][Full Text] [Related]
10. Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.
Marenne G; Rodríguez-Santiago B; Closas MG; Pérez-Jurado L; Rothman N; Rico D; Pita G; Pisano DG; Kogevinas M; Silverman DT; Valencia A; Real FX; Chanock SJ; Génin E; Malats N
Hum Mutat; 2011 Feb; 32(2):240-8. PubMed ID: 21089066
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.
Lin CF; Naj AC; Wang LS
Curr Protoc Hum Genet; 2013 Oct; 79():1.27.1-1.27.15. PubMed ID: 24510649
[TBL] [Abstract][Full Text] [Related]
14. Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs.
Seroussi E; Glick G; Shirak A; Yakobson E; Weller JI; Ezra E; Zeron Y
BMC Genomics; 2010 Nov; 11():673. PubMed ID: 21114805
[TBL] [Abstract][Full Text] [Related]
15. Assessing the reproducibility of exome copy number variations predictions.
Hong CS; Singh LN; Mullikin JC; Biesecker LG
Genome Med; 2016 Aug; 8(1):82. PubMed ID: 27503473
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
Zhao L; Bracken MB; DeWan AT
Ann Hum Genet; 2013 Jul; 77(4):277-87. PubMed ID: 23551011
[TBL] [Abstract][Full Text] [Related]
17. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Fromer M; Moran JL; Chambert K; Banks E; Bergen SE; Ruderfer DM; Handsaker RE; McCarroll SA; O'Donovan MC; Owen MJ; Kirov G; Sullivan PF; Hultman CM; Sklar P; Purcell SM
Am J Hum Genet; 2012 Oct; 91(4):597-607. PubMed ID: 23040492
[TBL] [Abstract][Full Text] [Related]
18. Twins, tissue, and time: an assessment of SNPs and CNVs.
Scheet P; Ehli EA; Xiao X; van Beijsterveldt CE; Abdellaoui A; Althoff RR; Hottenga JJ; Willemsen G; Nelson KA; Huizenga PE; Hu Y; Amos CI; Bartels M; Groen-Blokhuis MM; de Geus EJ; Hudziak JJ; Davies GE; Boomsma DI
Twin Res Hum Genet; 2012 Dec; 15(6):737-45. PubMed ID: 23021707
[TBL] [Abstract][Full Text] [Related]
19. Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.
Bae JS; Cheong HS; Chun JY; Park TJ; Kim JO; Kim EM; Park M; Kim DJ; Lee EJ; Kim EK; Lee JY; Shin HD
Ophthalmology; 2010 Jul; 117(7):1306-12.e4. PubMed ID: 20202685
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]