These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
132 related articles for article (PubMed ID: 26954760)
21. 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]
22. 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]
23. Stochastic segmentation models for array-based comparative genomic hybridization data analysis. Lai TL; Xing H; Zhang N Biostatistics; 2008 Apr; 9(2):290-307. PubMed ID: 17855472 [TBL] [Abstract][Full Text] [Related]
24. [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]
25. 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]
26. DNA Copy Number Selection Using Robust Structured Sparsity-Inducing Norms. Metsis V; Makedon F; Shen D; Huang H IEEE/ACM Trans Comput Biol Bioinform; 2014; 11(1):168-81. PubMed ID: 26355516 [TBL] [Abstract][Full Text] [Related]
27. iSeg: an efficient algorithm for segmentation of genomic and epigenomic data. Girimurugan SB; Liu Y; Lung PY; Vera DL; Dennis JH; Bass HW; Zhang J BMC Bioinformatics; 2018 Apr; 19(1):131. PubMed ID: 29642840 [TBL] [Abstract][Full Text] [Related]
28. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization. Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374 [TBL] [Abstract][Full Text] [Related]
29. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses. Machado IN; Heinrich JK; Barini R; Peralta CF Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218 [TBL] [Abstract][Full Text] [Related]
30. A fused lasso latent feature model for analyzing multi-sample aCGH data. Nowak G; Hastie T; Pollack JR; Tibshirani R Biostatistics; 2011 Oct; 12(4):776-91. PubMed ID: 21642389 [TBL] [Abstract][Full Text] [Related]
31. Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH. Hackmann K; Kuhlee F; Betcheva-Krajcir E; Kahlert AK; Mackenroth L; Klink B; Di Donato N; Tzschach A; Kast K; Wimberger P; Schrock E; Rump A Breast Cancer Res Treat; 2016 Oct; 159(3):585-90. PubMed ID: 27581129 [TBL] [Abstract][Full Text] [Related]
32. A stepwise framework for the normalization of array CGH data. Khojasteh M; Lam WL; Ward RK; MacAulay C BMC Bioinformatics; 2005 Nov; 6():274. PubMed ID: 16297240 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization. Repnikova EA; Rosenfeld JA; Bailes A; Weber C; Erdman L; McKinney A; Ramsey S; Hashimoto S; Lamb Thrush D; Astbury C; Reshmi SC; Shaffer LG; Gastier-Foster JM; Pyatt RE Forensic Sci Int Genet; 2013 Sep; 7(5):475-81. PubMed ID: 23948316 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. Classification of array CGH data using smoothed logistic regression model. Huang J; Salim A; Lei K; O'Sullivan K; Pawitan Y Stat Med; 2009 Dec; 28(30):3798-810. PubMed ID: 19856275 [TBL] [Abstract][Full Text] [Related]
37. PCR-Based Detection of DNA Copy Number Variation. Mehrotra M Methods Mol Biol; 2016; 1392():27-32. PubMed ID: 26843043 [TBL] [Abstract][Full Text] [Related]
38. Array CGH analysis of a cohort of Russian patients with intellectual disability. Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026 [TBL] [Abstract][Full Text] [Related]
39. Identification of significant regional genetic variations using continuous CNV values in aCGH data. Kim KY; Lee GY; Kim J; Jeung HC; Chung HC; Rha SY Genomics; 2009 Nov; 94(5):317-23. PubMed ID: 19699295 [TBL] [Abstract][Full Text] [Related]
40. Chromosomal copy number analysis in melanoma diagnostics. North JP; Vemula SS; Bastian BC Methods Mol Biol; 2014; 1102():199-226. PubMed ID: 24258981 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]