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.
140 related articles for article (PubMed ID: 30796811)
21. A comprehensive evaluation of alignment software for reduced representation bisulfite sequencing data. Sun X; Han Y; Zhou L; Chen E; Lu B; Liu Y; Pan X; Cowley AW; Liang M; Wu Q; Lu Y; Liu P Bioinformatics; 2018 Aug; 34(16):2715-2723. PubMed ID: 29579198 [TBL] [Abstract][Full Text] [Related]
22. A hybrid imputation approach for microarray missing value estimation. Li H; Zhao C; Shao F; Li GZ; Wang X BMC Genomics; 2015; 16 Suppl 9(Suppl 9):S1. PubMed ID: 26330180 [TBL] [Abstract][Full Text] [Related]
23. Tumor purity and differential methylation in cancer epigenomics. Wang F; Zhang N; Wang J; Wu H; Zheng X Brief Funct Genomics; 2016 Nov; 15(6):408-419. PubMed ID: 27199459 [TBL] [Abstract][Full Text] [Related]
24. Higher order methylation features for clustering and prediction in epigenomic studies. Kapourani CA; Sanguinetti G Bioinformatics; 2016 Sep; 32(17):i405-i412. PubMed ID: 27587656 [TBL] [Abstract][Full Text] [Related]
25. D3M: detection of differential distributions of methylation levels. Matsui Y; Mizuta M; Ito S; Miyano S; Shimamura T Bioinformatics; 2016 Aug; 32(15):2248-55. PubMed ID: 27153581 [TBL] [Abstract][Full Text] [Related]
26. Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA. Kennedy DW; White NM; Benton MC; Fox A; Scott RJ; Griffiths LR; Mengersen K; Lea RA PLoS One; 2018; 13(12):e0208915. PubMed ID: 30571772 [TBL] [Abstract][Full Text] [Related]
28. Complete deconvolution of DNA methylation signals from complex tissues: a geometric approach. Zhang W; Wu H; Li Z Bioinformatics; 2021 May; 37(8):1052-1059. PubMed ID: 33135072 [TBL] [Abstract][Full Text] [Related]
29. The influence of missing value imputation on detection of differentially expressed genes from microarray data. Scheel I; Aldrin M; Glad IK; Sørum R; Lyng H; Frigessi A Bioinformatics; 2005 Dec; 21(23):4272-9. PubMed ID: 16216830 [TBL] [Abstract][Full Text] [Related]
30. Collateral missing value imputation: a new robust missing value estimation algorithm for microarray data. Sehgal MS; Gondal I; Dooley LS Bioinformatics; 2005 May; 21(10):2417-23. PubMed ID: 15731210 [TBL] [Abstract][Full Text] [Related]
31. Imputation of missing covariate values in epigenome-wide analysis of DNA methylation data. Wu C; Demerath EW; Pankow JS; Bressler J; Fornage M; Grove ML; Chen W; Guan W Epigenetics; 2016; 11(2):132-9. PubMed ID: 26890800 [TBL] [Abstract][Full Text] [Related]
33. Differential methylation values in differential methylation analysis. Xie C; Leung YK; Chen A; Long DX; Hoyo C; Ho SM Bioinformatics; 2019 Apr; 35(7):1094-1097. PubMed ID: 30184051 [TBL] [Abstract][Full Text] [Related]
34. seqlm: an MDL based method for identifying differentially methylated regions in high density methylation array data. Kolde R; Märtens K; Lokk K; Laur S; Vilo J Bioinformatics; 2016 Sep; 32(17):2604-10. PubMed ID: 27187204 [TBL] [Abstract][Full Text] [Related]
35. Global analysis of methylation profiles from high resolution CpG data. Zhao N; Bell DA; Maity A; Staicu AM; Joubert BR; London SJ; Wu MC Genet Epidemiol; 2015 Feb; 39(2):53-64. PubMed ID: 25537884 [TBL] [Abstract][Full Text] [Related]
36. Human age estimation from blood using mRNA, DNA methylation, DNA rearrangement, and telomere length. Zubakov D; Liu F; Kokmeijer I; Choi Y; van Meurs JBJ; van IJcken WFJ; Uitterlinden AG; Hofman A; Broer L; van Duijn CM; Lewin J; Kayser M Forensic Sci Int Genet; 2016 Sep; 24():33-43. PubMed ID: 27288716 [TBL] [Abstract][Full Text] [Related]
37. Methylation-level inferences and detection of differential methylation with MeDIP-seq data. Zhou Y; Zhu J; Zhao M; Zhang B; Jiang C; Yang X PLoS One; 2018; 13(8):e0201586. PubMed ID: 30086146 [TBL] [Abstract][Full Text] [Related]
38. Evaluation of cross-platform and interlaboratory concordance via consensus modelling of genomic measurements. Peters TJ; French HJ; Bradford ST; Pidsley R; Stirzaker C; Varinli H; Nair S; Qu W; Song J; Giles KA; Statham AL; Speirs H; Speed TP; Clark SJ Bioinformatics; 2019 Feb; 35(4):560-570. PubMed ID: 30084929 [TBL] [Abstract][Full Text] [Related]
39. Ranking genomic features using an information-theoretic measure of epigenetic discordance. Jenkinson G; Abante J; Koldobskiy MA; Feinberg AP; Goutsias J BMC Bioinformatics; 2019 Apr; 20(1):175. PubMed ID: 30961526 [TBL] [Abstract][Full Text] [Related]
40. CopyNumber450kCancer: baseline correction for accurate copy number calling from the 450k methylation array. Marzouka NA; Nordlund J; Bäcklin CL; Lönnerholm G; Syvänen AC; Carlsson Almlöf J Bioinformatics; 2016 Apr; 32(7):1080-2. PubMed ID: 26553913 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]