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.
151 related articles for article (PubMed ID: 37072822)
1. The ENCODE Imputation Challenge: a critical assessment of methods for cross-cell type imputation of epigenomic profiles. Schreiber J; Boix C; Wook Lee J; Li H; Guan Y; Chang CC; Chang JC; Hawkins-Hooker A; Schölkopf B; Schweikert G; Carulla MR; Canakoglu A; Guzzo F; Nanni L; Masseroli M; Carman MJ; Pinoli P; Hong C; Yip KY; Spence JP; Batra SS; Song YS; Mahony S; Zhang Z; Tan W; Shen Y; Sun Y; Shi M; Adrian J; Sandstrom R; Farrell N; Halow J; Lee K; Jiang L; Yang X; Epstein C; Strattan JS; Bernstein B; Snyder M; Kellis M; Stafford W; Kundaje A; Genome Biol; 2023 Apr; 24(1):79. PubMed ID: 37072822 [TBL] [Abstract][Full Text] [Related]
2. Molgenis-impute: imputation pipeline in a box. Kanterakis A; Deelen P; van Dijk F; Byelas H; Dijkstra M; Swertz MA BMC Res Notes; 2015 Aug; 8():359. PubMed ID: 26286716 [TBL] [Abstract][Full Text] [Related]
3. Direct prediction of regulatory elements from partial data without imputation. Zhang Y; Mahony S PLoS Comput Biol; 2019 Nov; 15(11):e1007399. PubMed ID: 31682602 [TBL] [Abstract][Full Text] [Related]
5. DNA Methylation Imputation Across Platforms. Li G; Zhang G; Li Y Methods Mol Biol; 2022; 2432():137-151. PubMed ID: 35505213 [TBL] [Abstract][Full Text] [Related]
6. Exome sequence genotype imputation in globally diverse hexaploid wheat accessions. Shi F; Tibbits J; Pasam RK; Kay P; Wong D; Petkowski J; Forrest KL; Hayes BJ; Akhunova A; Davies J; Webb S; Spangenberg GC; Akhunov E; Hayden MJ; Daetwyler HD Theor Appl Genet; 2017 Jul; 130(7):1393-1404. PubMed ID: 28378053 [TBL] [Abstract][Full Text] [Related]
7. Advanced methods for missing values imputation based on similarity learning. Fouad KM; Ismail MM; Azar AT; Arafa MM PeerJ Comput Sci; 2021; 7():e619. PubMed ID: 34395861 [TBL] [Abstract][Full Text] [Related]
9. Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies. Hao K; Chudin E; McElwee J; Schadt EE BMC Genet; 2009 Jun; 10():27. PubMed ID: 19531258 [TBL] [Abstract][Full Text] [Related]
10. Missing value imputation in high-dimensional phenomic data: imputable or not, and how? Liao SG; Lin Y; Kang DD; Chandra D; Bon J; Kaminski N; Sciurba FC; Tseng GC BMC Bioinformatics; 2014 Nov; 15(1):346. PubMed ID: 25371041 [TBL] [Abstract][Full Text] [Related]
11. Imputing missing values for genetic interaction data. Wang Y; Wang L; Yang D; Deng M Methods; 2014 Jun; 67(3):269-77. PubMed ID: 24718098 [TBL] [Abstract][Full Text] [Related]
12. Highly Accurate and Efficient Data-Driven Methods for Genotype Imputation. Choudhury O; Chakrabarty A; Emrich SJ IEEE/ACM Trans Comput Biol Bioinform; 2019; 16(4):1107-1116. PubMed ID: 28574365 [TBL] [Abstract][Full Text] [Related]
13. Integration of genetic and clinical information to improve imputation of data missing from electronic health records. Li R; Chen Y; Moore JH J Am Med Inform Assoc; 2019 Oct; 26(10):1056-1063. PubMed ID: 31329892 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Impact of imputation methods on the amount of genetic variation captured by a single-nucleotide polymorphism panel in soybeans. Xavier A; Muir WM; Rainey KM BMC Bioinformatics; 2016 Feb; 17():55. PubMed ID: 26830693 [TBL] [Abstract][Full Text] [Related]
17. Prioritizing transcriptomic and epigenomic experiments using an optimization strategy that leverages imputed data. Schreiber J; Bilmes J; Noble WS Bioinformatics; 2021 May; 37(4):439-447. PubMed ID: 32966546 [TBL] [Abstract][Full Text] [Related]
18. Impact of genetic similarity on imputation accuracy. Roshyara NR; Scholz M BMC Genet; 2015 Jul; 16():90. PubMed ID: 26193934 [TBL] [Abstract][Full Text] [Related]
19. I-Impute: a self-consistent method to impute single cell RNA sequencing data. Feng X; Chen L; Wang Z; Li SC BMC Genomics; 2020 Nov; 21(Suppl 10):618. PubMed ID: 33208097 [TBL] [Abstract][Full Text] [Related]
20. Decoding regulatory structures and features from epigenomics profiles: A Roadmap-ENCODE Variational Auto-Encoder (RE-VAE) model. Hu R; Pei G; Jia P; Zhao Z Methods; 2021 May; 189():44-53. PubMed ID: 31672653 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]