199 related articles for article (PubMed ID: 30039360)
1. 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]
2. 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]
3. 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]
4. Evaluation of copy number variation detection for a SNP array platform.
Zhang X; Du R; Li S; Zhang F; Jin L; Wang H
BMC Bioinformatics; 2014 Feb; 15():50. PubMed ID: 24555668
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Copy Number Variation Detection via High-Density SNP Genotyping.
Wang K; Bucan M
CSH Protoc; 2008 Jun; 2008():pdb.top46. PubMed ID: 21356857
[TBL] [Abstract][Full Text] [Related]
8. HaplotypeCN: copy number haplotype inference with Hidden Markov Model and localized haplotype clustering.
Lin YJ; Chen YT; Hsu SN; Peng CH; Tang CY; Yen TC; Hsieh WP
PLoS One; 2014; 9(5):e96841. PubMed ID: 24849202
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genomic and genetic variability of six chicken populations using single nucleotide polymorphism and copy number variants as markers.
Strillacci MG; Cozzi MC; Gorla E; Mosca F; Schiavini F; Román-Ponce SI; Ruiz López FJ; Schiavone A; Marzoni M; Cerolini S; Bagnato A
Animal; 2017 May; 11(5):737-745. PubMed ID: 27819220
[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. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. Accuracy of CNV Detection from GWAS Data.
Zhang D; Qian Y; Akula N; Alliey-Rodriguez N; Tang J; ; Gershon ES; Liu C
PLoS One; 2011 Jan; 6(1):e14511. PubMed ID: 21249187
[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. Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
Lin CH; Huang MC; Li LH; Wu JY; Chen YT; Fann CS
Hum Mutat; 2008 Aug; 29(8):1055-62. PubMed ID: 18470944
[TBL] [Abstract][Full Text] [Related]
20. CNstream: a method for the identification and genotyping of copy number polymorphisms using Illumina microarrays.
Alonso A; Julià A; Tortosa R; Canaleta C; Cañete JD; Ballina J; Balsa A; Tornero J; Marsal S
BMC Bioinformatics; 2010 May; 11():264. PubMed ID: 20482829
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
