Transcript Variant Calling is a computational method within transcript sequence analysis that identifies and characterizes alternative splicing events and nucleotide-level variations in RNA sequences relative to a reference genome or transcriptome.
14
Publications
1.4K
Citations
66
Authors
28
Institutions
Publications per year
2017–2026
6
Parents
Publications
14
Genetic Architecture of Transcript-Level Variation in Humans
Shiwei Duan, R. Stephanie Huang, Wei Zhang et al. · The American Journal of Human Genetics · 2008 · 134 citations · Full text
RVboost: RNA-seq variants prioritization using a boosting method
Chen Wang, Jaime Davila, Saurabh Baheti et al. · Bioinformatics · 2014 · 67 citations · Full text
1–5 of 14
Authors
66
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- RG
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1–5 of 66
Institutions
28
Centre for Human Genetics
Oxford, United Kingdom
2 h-index
2 publications
66 citations
Johns Hopkins University
Baltimore, United States
2 h-index
6 publications
300 citations
Johns Hopkins Medicine
Baltimore, United States
2 h-index
4 publications
272 citations
Pfizer (United States)
New York, United States
2 h-index
2 publications
66 citations
University of Turin
Turin, Italy
2 h-index
2 publications
66 citations
University of Oxford
Oxford, United Kingdom
2 h-index
2 publications
66 citations
Institute of Cancer Research
London, United Kingdom
2 h-index
2 publications
66 citations
UNSW Sydney
Sydney, Australia
1 h-index
1 publications
30 citations
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Venues
- PLoS ONE
2 publications · 38 citations
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- Wellcome Open Research
2 publications · 66 citations
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- Bioinformatics
1 publications · 67 citations
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- Nature
1 publications · 828 citations
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- bioRxiv (Cold Spring Harbor Laboratory)
Repository · 1 publications · 14 citations
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