942 related articles for article (PubMed ID: 28438122)
1. 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]
2. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
[TBL] [Abstract][Full Text] [Related]
3. Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis.
Zhou B; Ho SS; Zhang X; Pattni R; Haraksingh RR; Urban AE
J Med Genet; 2018 Nov; 55(11):735-743. PubMed ID: 30061371
[TBL] [Abstract][Full Text] [Related]
4. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
[TBL] [Abstract][Full Text] [Related]
7. Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays.
Oldridge DA; Banerjee S; Setlur SR; Sboner A; Demichelis F
Nucleic Acids Res; 2010 Jun; 38(10):3275-86. PubMed ID: 20156996
[TBL] [Abstract][Full Text] [Related]
8. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
Tucker T; Montpetit A; Chai D; Chan S; Chénier S; Coe BP; Delaney A; Eydoux P; Lam WL; Langlois S; Lemyre E; Marra M; Qian H; Rouleau GA; Vincent D; Michaud JL; Friedman JM
BMC Med Genomics; 2011 Mar; 4():25. PubMed ID: 21439053
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays.
Goodman CW; Major HJ; Walls WD; Sheffield VC; Casavant TL; Darbro BW
J Biomed Inform; 2015 Apr; 54():106-13. PubMed ID: 25595567
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Copy number variants in the sheep genome detected using multiple approaches.
Jenkins GM; Goddard ME; Black MA; Brauning R; Auvray B; Dodds KG; Kijas JW; Cockett N; McEwan JC
BMC Genomics; 2016 Jun; 17():441. PubMed ID: 27277319
[TBL] [Abstract][Full Text] [Related]
16. An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.
Huang MC; Chuang TP; Chen CH; Wu JY; Chen YT; Li LH; Yang HC
BMC Genomics; 2016 Mar; 17():266. PubMed ID: 27029637
[TBL] [Abstract][Full Text] [Related]
17. Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms.
Rao J; Peng L; Liang X; Jiang H; Geng C; Zhao X; Liu X; Fan G; Chen F; Mu F
BMC Bioinformatics; 2020 Nov; 21(1):518. PubMed ID: 33176676
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive characterization of copy number variation (CNV) called from array, long- and short-read data.
Lavrichenko K; Johansson S; Jonassen I
BMC Genomics; 2021 Nov; 22(1):826. PubMed ID: 34789167
[TBL] [Abstract][Full Text] [Related]
19. Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
Valsesia A; Stevenson BJ; Waterworth D; Mooser V; Vollenweider P; Waeber G; Jongeneel CV; Beckmann JS; Kutalik Z; Bergmann S
BMC Genomics; 2012 Jun; 13():241. PubMed ID: 22702538
[TBL] [Abstract][Full Text] [Related]
20. Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.
Wong G; Leckie C; Gorringe KL; Haviv I; Campbell IG; Kowalczyk A
Bioinformatics; 2010 Apr; 26(8):1007-14. PubMed ID: 20189937
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
