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.
495 related articles for article (PubMed ID: 36478271)
21. IDP-denovo: de novo transcriptome assembly and isoform annotation by hybrid sequencing. Fu S; Ma Y; Yao H; Xu Z; Chen S; Song J; Au KF Bioinformatics; 2018 Jul; 34(13):2168-2176. PubMed ID: 29905763 [TBL] [Abstract][Full Text] [Related]
22. Inference of isoforms from short sequence reads. Feng J; Li W; Jiang T J Comput Biol; 2011 Mar; 18(3):305-21. PubMed ID: 21385036 [TBL] [Abstract][Full Text] [Related]
24. A comprehensive long-read isoform analysis platform and sequencing resource for breast cancer. Veiga DFT; Nesta A; Zhao Y; Deslattes Mays A; Huynh R; Rossi R; Wu TC; Palucka K; Anczukow O; Beck CR; Banchereau J Sci Adv; 2022 Jan; 8(3):eabg6711. PubMed ID: 35044822 [TBL] [Abstract][Full Text] [Related]
25. Sparse linear modeling of next-generation mRNA sequencing (RNA-Seq) data for isoform discovery and abundance estimation. Li JJ; Jiang CR; Brown JB; Huang H; Bickel PJ Proc Natl Acad Sci U S A; 2011 Dec; 108(50):19867-72. PubMed ID: 22135461 [TBL] [Abstract][Full Text] [Related]
27. Exploring differential exon usage via short- and long-read RNA sequencing strategies. Leshkowitz D; Kedmi M; Fried Y; Pilzer D; Keren-Shaul H; Ainbinder E; Dassa B Open Biol; 2022 Sep; 12(9):220206. PubMed ID: 36168804 [TBL] [Abstract][Full Text] [Related]
28. Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer. Liu S; Wu I; Yu YP; Balamotis M; Ren B; Ben Yehezkel T; Luo JH Commun Biol; 2021 Apr; 4(1):506. PubMed ID: 33907296 [TBL] [Abstract][Full Text] [Related]
29. ORMAN: optimal resolution of ambiguous RNA-Seq multimappings in the presence of novel isoforms. Dao P; Numanagić I; Lin YY; Hach F; Karakoc E; Donmez N; Collins C; Eichler EE; Sahinalp SC Bioinformatics; 2014 Mar; 30(5):644-51. PubMed ID: 24130305 [TBL] [Abstract][Full Text] [Related]
30. Highly efficient clustering of long-read transcriptomic data with GeLuster. Ma J; Zhao X; Qi E; Han R; Yu T; Li G Bioinformatics; 2024 Feb; 40(2):. PubMed ID: 38310330 [TBL] [Abstract][Full Text] [Related]
31. Information transduction capacity reduces the uncertainties in annotation-free isoform discovery and quantification. Deng Y; Bao F; Yang Y; Ji X; Du M; Zhang Z; Wang M; Dai Q Nucleic Acids Res; 2017 Sep; 45(15):e143. PubMed ID: 28911101 [TBL] [Abstract][Full Text] [Related]
32. Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome. Tilgner H; Jahanbani F; Gupta I; Collier P; Wei E; Rasmussen M; Snyder M Genome Res; 2018 Feb; 28(2):231-242. PubMed ID: 29196558 [TBL] [Abstract][Full Text] [Related]
33. SplicingCompass: differential splicing detection using RNA-seq data. Aschoff M; Hotz-Wagenblatt A; Glatting KH; Fischer M; Eils R; König R Bioinformatics; 2013 May; 29(9):1141-8. PubMed ID: 23449093 [TBL] [Abstract][Full Text] [Related]
34. Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity. Miller AR; Wijeratne S; McGrath SD; Schieffer KM; Miller KE; Lee K; Mathew M; LaHaye S; Fitch JR; Kelly BJ; White P; Mardis ER; Wilson RK; Cottrell CE; Magrini V J Mol Diagn; 2022 Dec; 24(12):1292-1306. PubMed ID: 36191838 [TBL] [Abstract][Full Text] [Related]
35. Alternative Splicing Signatures in RNA-seq Data: Percent Spliced in (PSI). Schafer S; Miao K; Benson CC; Heinig M; Cook SA; Hubner N Curr Protoc Hum Genet; 2015 Oct; 87():11.16.1-11.16.14. PubMed ID: 26439713 [TBL] [Abstract][Full Text] [Related]
36. ASGAL: aligning RNA-Seq data to a splicing graph to detect novel alternative splicing events. Denti L; Rizzi R; Beretta S; Vedova GD; Previtali M; Bonizzoni P BMC Bioinformatics; 2018 Nov; 19(1):444. PubMed ID: 30458725 [TBL] [Abstract][Full Text] [Related]
37. SpliceNet: recovering splicing isoform-specific differential gene networks from RNA-Seq data of normal and diseased samples. Yalamanchili HK; Li Z; Wang P; Wong MP; Yao J; Wang J Nucleic Acids Res; 2014 Sep; 42(15):e121. PubMed ID: 25034693 [TBL] [Abstract][Full Text] [Related]
38. IFDlong: an isoform and fusion detector for accurate annotation and quantification of long-read RNA-seq data. Wang W; Li Y; Ko S; Feng N; Zhang M; Liu JJ; Zheng S; Ren B; Yu YP; Luo JH; Tseng GC; Liu S bioRxiv; 2024 May; ():. PubMed ID: 38798496 [TBL] [Abstract][Full Text] [Related]
39. Comprehensive assessment of mRNA isoform detection methods for long-read sequencing data. Su Y; Yu Z; Jin S; Ai Z; Yuan R; Chen X; Xue Z; Guo Y; Chen D; Liang H; Liu Z; Liu W Nat Commun; 2024 May; 15(1):3972. PubMed ID: 38730241 [TBL] [Abstract][Full Text] [Related]
40. Nanoblot: an R-package for visualization of RNA isoforms from long-read RNA-sequencing data. DeMario S; Xu K; He K; Chanfreau GF RNA; 2023 Aug; 29(8):1099-1107. PubMed ID: 37137666 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]