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.
200 related articles for article (PubMed ID: 30096157)
1. iMapSplice: Alleviating reference bias through personalized RNA-seq alignment. Liu X; MacLeod JN; Liu J PLoS One; 2018; 13(8):e0201554. PubMed ID: 30096157 [TBL] [Abstract][Full Text] [Related]
2. Using RNA-Seq to Discover Genetic Polymorphisms That Produce Hidden Splice Variants. Stein S; Bahrami-Samani E; Xing Y Methods Mol Biol; 2017; 1648():129-142. PubMed ID: 28766294 [TBL] [Abstract][Full Text] [Related]
3. Discover hidden splicing variations by mapping personal transcriptomes to personal genomes. Stein S; Lu ZX; Bahrami-Samani E; Park JW; Xing Y Nucleic Acids Res; 2015 Dec; 43(22):10612-22. PubMed ID: 26578562 [TBL] [Abstract][Full Text] [Related]
4. Discerning novel splice junctions derived from RNA-seq alignment: a deep learning approach. Zhang Y; Liu X; MacLeod J; Liu J BMC Genomics; 2018 Dec; 19(1):971. PubMed ID: 30591034 [TBL] [Abstract][Full Text] [Related]
5. PASSion: a pattern growth algorithm-based pipeline for splice junction detection in paired-end RNA-Seq data. Zhang Y; Lameijer EW; 't Hoen PA; Ning Z; Slagboom PE; Ye K Bioinformatics; 2012 Feb; 28(4):479-86. PubMed ID: 22219203 [TBL] [Abstract][Full Text] [Related]
10. ASElux: an ultra-fast and accurate allelic reads counter. Miao Z; Alvarez M; Pajukanta P; Ko A Bioinformatics; 2018 Apr; 34(8):1313-1320. PubMed ID: 29186329 [TBL] [Abstract][Full Text] [Related]
11. JAGuaR: junction alignments to genome for RNA-seq reads. Butterfield YS; Kreitzman M; Thiessen N; Corbett RD; Li Y; Pang J; Ma YP; Jones SJ; Birol İ PLoS One; 2014; 9(7):e102398. PubMed ID: 25062255 [TBL] [Abstract][Full Text] [Related]