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.
176 related articles for article (PubMed ID: 32293520)
1. Obstacles to detecting isoforms using full-length scRNA-seq data. Westoby J; Artemov P; Hemberg M; Ferguson-Smith A Genome Biol; 2020 Mar; 21(1):74. PubMed ID: 32293520 [TBL] [Abstract][Full Text] [Related]
2. Detecting differential alternative splicing events in scRNA-seq with or without Unique Molecular Identifiers. Hu Y; Wang K; Li M PLoS Comput Biol; 2020 Jun; 16(6):e1007925. PubMed ID: 32502143 [TBL] [Abstract][Full Text] [Related]
3. Simulation-based benchmarking of isoform quantification in single-cell RNA-seq. Westoby J; Herrera MS; Ferguson-Smith AC; Hemberg M Genome Biol; 2018 Nov; 19(1):191. PubMed ID: 30404663 [TBL] [Abstract][Full Text] [Related]
4. Using BRIE to Detect and Analyze Splicing Isoforms in scRNA-Seq Data. Huang Y; Sanguinetti G Methods Mol Biol; 2019; 1935():175-185. PubMed ID: 30758827 [TBL] [Abstract][Full Text] [Related]
5. BRIE: transcriptome-wide splicing quantification in single cells. Huang Y; Sanguinetti G Genome Biol; 2017 Jun; 18(1):123. PubMed ID: 28655331 [TBL] [Abstract][Full Text] [Related]
6. Coverage-dependent bias creates the appearance of binary splicing in single cells. Buen Abad Najar CF; Yosef N; Lareau LF Elife; 2020 Jun; 9():. PubMed ID: 32597758 [TBL] [Abstract][Full Text] [Related]
7. A convex formulation for joint RNA isoform detection and quantification from multiple RNA-seq samples. Bernard E; Jacob L; Mairal J; Viara E; Vert JP BMC Bioinformatics; 2015 Aug; 16():262. PubMed ID: 26286719 [TBL] [Abstract][Full Text] [Related]
8. A multitask clustering approach for single-cell RNA-seq analysis in Recessive Dystrophic Epidermolysis Bullosa. Zhang H; Lee CAA; Li Z; Garbe JR; Eide CR; Petegrosso R; Kuang R; Tolar J PLoS Comput Biol; 2018 Apr; 14(4):e1006053. PubMed ID: 29630593 [TBL] [Abstract][Full Text] [Related]
9. TIGAR: transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference. Nariai N; Hirose O; Kojima K; Nagasaki M Bioinformatics; 2013 Sep; 29(18):2292-9. PubMed ID: 23821651 [TBL] [Abstract][Full Text] [Related]
10. Mining alternative splicing patterns in scRNA-seq data using scASfind. Song Y; Parada G; Lee JTH; Hemberg M Genome Biol; 2024 Jul; 25(1):197. PubMed ID: 39075577 [TBL] [Abstract][Full Text] [Related]
11. IUTA: a tool for effectively detecting differential isoform usage from RNA-Seq data. Niu L; Huang W; Umbach DM; Li L BMC Genomics; 2014 Oct; 15(1):862. PubMed ID: 25283306 [TBL] [Abstract][Full Text] [Related]
12. Bulk and single-cell alternative splicing analyses reveal roles of TRA2B in myogenic differentiation. Chen G; Chen J; Qi L; Yin Y; Lin Z; Wen H; Zhang S; Xiao C; Bello SF; Zhang X; Nie Q; Luo W Cell Prolif; 2024 Feb; 57(2):e13545. PubMed ID: 37705195 [TBL] [Abstract][Full Text] [Related]
13. Multiplexed primer extension sequencing: A targeted RNA-seq method that enables high-precision quantitation of mRNA splicing isoforms and rare pre-mRNA splicing intermediates. Gildea MA; Dwyer ZW; Pleiss JA Methods; 2020 Apr; 176():34-45. PubMed ID: 31121301 [TBL] [Abstract][Full Text] [Related]
14. Robustness and applicability of transcription factor and pathway analysis tools on single-cell RNA-seq data. Holland CH; Tanevski J; Perales-Patón J; Gleixner J; Kumar MP; Mereu E; Joughin BA; Stegle O; Lauffenburger DA; Heyn H; Szalai B; Saez-Rodriguez J Genome Biol; 2020 Feb; 21(1):36. PubMed ID: 32051003 [TBL] [Abstract][Full Text] [Related]
15. Mapping and modeling the genomic basis of differential RNA isoform expression at single-cell resolution with LR-Split-seq. Rebboah E; Reese F; Williams K; Balderrama-Gutierrez G; McGill C; Trout D; Rodriguez I; Liang H; Wold BJ; Mortazavi A Genome Biol; 2021 Oct; 22(1):286. PubMed ID: 34620214 [TBL] [Abstract][Full Text] [Related]
16. A novel method for single-cell data imputation using subspace regression. Tran D; Tran B; Nguyen H; Nguyen T Sci Rep; 2022 Feb; 12(1):2697. PubMed ID: 35177662 [TBL] [Abstract][Full Text] [Related]
17. SCC: an accurate imputation method for scRNA-seq dropouts based on a mixture model. Zheng Y; Zhong Y; Hu J; Shang X BMC Bioinformatics; 2021 Jan; 22(1):5. PubMed ID: 33407064 [TBL] [Abstract][Full Text] [Related]
18. Studying Isoform-Specific mRNA Recruitment to Polyribosomes with Frac-seq. Martinez-Nunez RT; Sanford JR Methods Mol Biol; 2016; 1358():99-108. PubMed ID: 26463379 [TBL] [Abstract][Full Text] [Related]
19. IsoCell: An Approach to Enhance Single Cell Clustering by Integrating Isoform-Level Expression Through Orthogonal Projection. Liu Y; Li HD; Xu Y; Liu YW; Peng X; Wang J IEEE/ACM Trans Comput Biol Bioinform; 2023; 20(1):465-475. PubMed ID: 35100120 [TBL] [Abstract][Full Text] [Related]
20. Isoform Evolution in Primates through Independent Combination of Alternative RNA Processing Events. Zhang SJ; Wang C; Yan S; Fu A; Luan X; Li Y; Sunny Shen Q; Zhong X; Chen JY; Wang X; Chin-Ming Tan B; He A; Li CY Mol Biol Evol; 2017 Oct; 34(10):2453-2468. PubMed ID: 28957512 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]