572 related articles for article (PubMed ID: 26197066)
1. 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]
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. 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]
4. 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]
5. An integrative segmentation method for detecting germline copy number variations in SNP arrays.
Shi J; Li P
Genet Epidemiol; 2012 May; 36(4):373-83. PubMed ID: 22539397
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Characterization of copy number variants in a large multibreed population of beef and dairy cattle using high-density single nucleotide polymorphism genotype data.
Rafter P; Purfield DC; Berry DP; Parnell AC; Gormley IC; Kearney JF; Coffey MP; Carthy TR
J Anim Sci; 2018 Sep; 96(10):4112-4124. PubMed ID: 30239746
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of copy number variation using SNP genotyping.
Cooper GM; Mefford HC
Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
[TBL] [Abstract][Full Text] [Related]
11. Copy number variation accuracy in genome-wide association studies.
Lin P; Hartz SM; Wang JC; Krueger RF; Foroud TM; Edenberg HJ; Nurnberger JI; Brooks AI; Tischfield JA; Almasy L; Webb BT; Hesselbrock VM; Porjesz B; Goate AM; Bierut LJ; Rice JP; ; ;
Hum Hered; 2011; 71(3):141-7. PubMed ID: 21778733
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. PennCNV in whole-genome sequencing data.
de Araújo Lima L; Wang K
BMC Bioinformatics; 2017 Oct; 18(Suppl 11):383. PubMed ID: 28984186
[TBL] [Abstract][Full Text] [Related]
15. Application of Nexus copy number software for CNV detection and analysis.
Darvishi K
Curr Protoc Hum Genet; 2010 Apr; Chapter 4():Unit 4.14.1-28. PubMed ID: 20373515
[TBL] [Abstract][Full Text] [Related]
16. COKGEN: a software for the identification of rare copy number variation from SNP microarrays.
Yavaş G; Koyutürk M; Ozsoyoğlu M; Gould MP; Laframboise T
Pac Symp Biocomput; 2010; ():371-82. PubMed ID: 19908389
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. X-CNV: genome-wide prediction of the pathogenicity of copy number variations.
Zhang L; Shi J; Ouyang J; Zhang R; Tao Y; Yuan D; Lv C; Wang R; Ning B; Roberts R; Tong W; Liu Z; Shi T
Genome Med; 2021 Aug; 13(1):132. PubMed ID: 34407882
[TBL] [Abstract][Full Text] [Related]
19. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing.
Onsongo G; Baughn LB; Bower M; Henzler C; Schomaker M; Silverstein KA; Thyagarajan B
J Mol Diagn; 2016 Nov; 18(6):872-881. PubMed ID: 27597741
[TBL] [Abstract][Full Text] [Related]
20. Noise cancellation using total variation for copy number variation detection.
Zare F; Hosny A; Nabavi S
BMC Bioinformatics; 2018 Oct; 19(Suppl 11):361. PubMed ID: 30343665
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
