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.
23. Microarray comparative genomic hybridization reveals genome-wide patterns of DNA gains and losses in post-Chernobyl thyroid cancer. Kimmel RR; Zhao LP; Nguyen D; Lee S; Aronszajn M; Cheng C; Troshin VP; Abrosimov A; Delrow J; Tuttle RM; Tsyb AF; Kopecky KJ; Davis S; Neiman PE Radiat Res; 2006 Sep; 166(3):519-31. PubMed ID: 16953671 [TBL] [Abstract][Full Text] [Related]
24. Detection and validation of single gene inversions. Lefebvre JF; El-Mabrouk N; Tillier E; Sankoff D Bioinformatics; 2003; 19 Suppl 1():i190-6. PubMed ID: 12855457 [TBL] [Abstract][Full Text] [Related]
25. BioHMM: a heterogeneous hidden Markov model for segmenting array CGH data. Marioni JC; Thorne NP; Tavaré S Bioinformatics; 2006 May; 22(9):1144-6. PubMed ID: 16533818 [TBL] [Abstract][Full Text] [Related]
26. Fast and sensitive alignment of large genomic sequences. Brudno M; Morgenstern B Proc IEEE Comput Soc Bioinform Conf; 2002; 1():138-47. PubMed ID: 15838131 [TBL] [Abstract][Full Text] [Related]
27. Continuous-index hidden Markov modelling of array CGH copy number data. Stjernqvist S; Rydén T; Sköld M; Staaf J Bioinformatics; 2007 Apr; 23(8):1006-14. PubMed ID: 17309894 [TBL] [Abstract][Full Text] [Related]
30. A probe-density-based analysis method for array CGH data: simulation, normalization and centralization. Chen HI; Hsu FH; Jiang Y; Tsai MH; Yang PC; Meltzer PS; Chuang EY; Chen Y Bioinformatics; 2008 Aug; 24(16):1749-56. PubMed ID: 18603568 [TBL] [Abstract][Full Text] [Related]
31. Estimation of correlations between copy-number variants in non-coding DNA. Stamoulis C Annu Int Conf IEEE Eng Med Biol Soc; 2011; 2011():5563-6. PubMed ID: 22255599 [TBL] [Abstract][Full Text] [Related]
33. Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data. Lai WR; Johnson MD; Kucherlapati R; Park PJ Bioinformatics; 2005 Oct; 21(19):3763-70. PubMed ID: 16081473 [TBL] [Abstract][Full Text] [Related]
34. Efficient sorting of genomic permutations by translocation, inversion and block interchange. Yancopoulos S; Attie O; Friedberg R Bioinformatics; 2005 Aug; 21(16):3340-6. PubMed ID: 15951307 [TBL] [Abstract][Full Text] [Related]
35. Detection of low level genomic alterations by comparative genomic hybridization based on cDNA micro-arrays. Bilke S; Chen QR; Whiteford CC; Khan J Bioinformatics; 2005 Apr; 21(7):1138-45. PubMed ID: 15539449 [TBL] [Abstract][Full Text] [Related]
36. Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis. Kirchhoff M; Gerdes T; Maahr J; Rose H; Lundsteen C Cytometry; 1997 Jun; 28(2):130-4. PubMed ID: 9181302 [TBL] [Abstract][Full Text] [Related]
37. ArrayCyGHt: a web application for analysis and visualization of array-CGH data. Kim SY; Nam SW; Lee SH; Park WS; Yoo NJ; Lee JY; Chung YJ Bioinformatics; 2005 May; 21(10):2554-5. PubMed ID: 15746288 [TBL] [Abstract][Full Text] [Related]
38. Allelic dosage analysis with genotyping microarrays. Ishikawa S; Komura D; Tsuji S; Nishimura K; Yamamoto S; Panda B; Huang J; Fukayama M; Jones KW; Aburatani H Biochem Biophys Res Commun; 2005 Aug; 333(4):1309-14. PubMed ID: 15982637 [TBL] [Abstract][Full Text] [Related]
39. Detection of gene copy number changes in CGH microarrays using a spatially correlated mixture model. Broët P; Richardson S Bioinformatics; 2006 Apr; 22(8):911-8. PubMed ID: 16455750 [TBL] [Abstract][Full Text] [Related]
40. Discovering and detecting transposable elements in genome sequences. Bergman CM; Quesneville H Brief Bioinform; 2007 Nov; 8(6):382-92. PubMed ID: 17932080 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]