391 related articles for article (PubMed ID: 20373515)
1. 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]
2. 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]
3. 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]
4. 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]
5. Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.
Wiszniewska J; Bi W; Shaw C; Stankiewicz P; Kang SH; Pursley AN; Lalani S; Hixson P; Gambin T; Tsai CH; Bock HG; Descartes M; Probst FJ; Scaglia F; Beaudet AL; Lupski JR; Eng C; Cheung SW; Bacino C; Patel A
Eur J Hum Genet; 2014 Jan; 22(1):79-87. PubMed ID: 23695279
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Array-Based Comparative Genomic Hybridization (aCGH).
Zhang C; Cerveira E; Romanovitch M; Zhu Q
Methods Mol Biol; 2017; 1541():167-179. PubMed ID: 27910023
[TBL] [Abstract][Full Text] [Related]
8. Copy number variations and stroke.
Colaianni V; Mazzei R; Cavallaro S
Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation.
Karimpour-Fard A; Dumas L; Phang T; Sikela JM; Hunter LE
Hum Genomics; 2010 Aug; 4(6):421-7. PubMed ID: 20846932
[TBL] [Abstract][Full Text] [Related]
13. Novel applications of array comparative genomic hybridization in molecular diagnostics.
Cheung SW; Bi W
Expert Rev Mol Diagn; 2018 Jun; 18(6):531-542. PubMed ID: 29848116
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Array comparative genomic hybridization (array CGH) for detection of genomic copy number variants.
Ahn JW; Coldwell M; Bint S; Mackie Ogilvie C
J Vis Exp; 2015 Feb; (96):e51718. PubMed ID: 25742425
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Detection of copy number variations in melanocytic lesions utilising array based comparative genomic hybridisation.
Mesbah Ardakani N; Thomas C; Robinson C; Mina K; Harvey NT; Amanuel B; Wood BA
Pathology; 2017 Apr; 49(3):285-291. PubMed ID: 28274670
[TBL] [Abstract][Full Text] [Related]
19. SNP genotyping with the next generation of CGH microarray.
Burton R
MLO Med Lab Obs; 2013 Jul; 45(7):8, 10, 12 passim. PubMed ID: 24180067
[TBL] [Abstract][Full Text] [Related]
20. Current analysis platforms and methods for detecting copy number variation.
Li W; Olivier M
Physiol Genomics; 2013 Jan; 45(1):1-16. PubMed ID: 23132758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]