225 related articles for article (PubMed ID: 22046040)
1. Comparative genomic hybridization to detect variation in the copy number of large DNA segments.
Holcomb IN; Trask BJ
Cold Spring Harb Protoc; 2011 Nov; 2011(11):1323-33. PubMed ID: 22046040
[TBL] [Abstract][Full Text] [Related]
2. [Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].
Wang Y; Ma DY; Yang YQ; Zhou J; Zhou XY; Ji XQ; Chen J; Cao L; Hu P; Xu ZF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):439-42. PubMed ID: 22875502
[TBL] [Abstract][Full Text] [Related]
3. CNVDetector: locating copy number variations using array CGH data.
Chen PA; Liu HF; Chao KM
Bioinformatics; 2008 Dec; 24(23):2773-5. PubMed ID: 18842603
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of the efficacy of constitutional array-based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA.
Tan NH; Palmer R; Wang R
J Obstet Gynaecol Res; 2010 Feb; 36(1):19-26. PubMed ID: 20178523
[TBL] [Abstract][Full Text] [Related]
5. Multiplex Amplifiable Probe Hybridization (MAPH) methodology as an alternative to comparative genomic hybridization (CGH).
Kousoulidou L; Sismani C; Patsalis PC
Methods Mol Biol; 2010; 653():47-71. PubMed ID: 20721737
[TBL] [Abstract][Full Text] [Related]
6. Interpretation of array comparative genome hybridization data: a major challenge.
Gijsbers AC; Schoumans J; Ruivenkamp CA
Cytogenet Genome Res; 2011; 135(3-4):222-7. PubMed ID: 22086107
[TBL] [Abstract][Full Text] [Related]
7. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
[TBL] [Abstract][Full Text] [Related]
8. SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization data.
Chi B; DeLeeuw RJ; Coe BP; MacAulay C; Lam WL
BMC Bioinformatics; 2004 Feb; 5():13. PubMed ID: 15040819
[TBL] [Abstract][Full Text] [Related]
9. The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome.
Przybytkowski E; Ferrario C; Basik M
BMC Med Genomics; 2011 Jan; 4():16. PubMed ID: 21272361
[TBL] [Abstract][Full Text] [Related]
10. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
11. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
[TBL] [Abstract][Full Text] [Related]
12. CAM: a web tool for combining array CGH and microarray gene expression data from multiple samples.
Oh M; Song B; Lee H
Comput Biol Med; 2010 Sep; 40(9):781-5. PubMed ID: 20728879
[TBL] [Abstract][Full Text] [Related]
13. Across array comparative genomic hybridization: a strategy to reduce reference channel hybridizations.
Buffart TE; Israeli D; Tijssen M; Vosse SJ; Mrsić A; Meijer GA; Ylstra B
Genes Chromosomes Cancer; 2008 Nov; 47(11):994-1004. PubMed ID: 18663753
[TBL] [Abstract][Full Text] [Related]
14. Computational methods for identification of recurrent copy number alteration patterns by array CGH.
Shah SP
Cytogenet Genome Res; 2008; 123(1-4):343-51. PubMed ID: 19287173
[TBL] [Abstract][Full Text] [Related]
15. Pharmacogenetics: technologies to detect copy number variations.
Dhawan D; Padh H
Curr Opin Mol Ther; 2009 Dec; 11(6):670-80. PubMed ID: 20072944
[TBL] [Abstract][Full Text] [Related]
16. Array-based comparative genomic hybridization as a tool for analyzing the leukemia genome.
Strefford JC; Parker H
Methods Mol Biol; 2009; 538():151-77. PubMed ID: 19277573
[TBL] [Abstract][Full Text] [Related]
17. Genetic predisposition in degenerative lumbar scoliosis due to the copy number variation.
Shin JH; Ha KY; Jung SH; Chung YJ
Spine (Phila Pa 1976); 2011 Oct; 36(21):1782-93. PubMed ID: 21587107
[TBL] [Abstract][Full Text] [Related]
18. CGcgh: a tool for molecular karyotyping using DNA microarray-based comparative genomic hybridization (array-CGH).
Lee YS; Chao A; Chao AS; Chang SD; Chen CH; Wu WM; Wang TH; Wang HS
J Biomed Sci; 2008 Nov; 15(6):687-96. PubMed ID: 18712492
[TBL] [Abstract][Full Text] [Related]
19. Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.
Aboura A; Dupas C; Tachdjian G; Portnoï MF; Bourcigaux N; Dewailly D; Frydman R; Fauser B; Ronci-Chaix N; Donadille B; Bouchard P; Christin-Maitre S
J Clin Endocrinol Metab; 2009 Nov; 94(11):4540-6. PubMed ID: 19837940
[TBL] [Abstract][Full Text] [Related]
20. Genomic changes detected by array CGH in human embryos with developmental defects.
Rajcan-Separovic E; Qiao Y; Tyson C; Harvard C; Fawcett C; Kalousek D; Stephenson M; Philipp T
Mol Hum Reprod; 2010 Feb; 16(2):125-34. PubMed ID: 19778950
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
