Splice Variant Annotation
Splice Variant Annotation is a computational or bioinformatics methodology that systematically identifies, classifies, and characterizes alternatively spliced transcript isoforms by mapping exon-intron structures to genomic sequences and delineating their functional and structural distinctions.
302
Publications
43.2K
Citations
2.1K
Authors
640
Institutions
Publications per year
2017–2026
67
302
TopHat: discovering splice junctions with RNA-Seq
Cole Trapnell, Lior Pachter, Steven L. Salzberg · Bioinformatics · 2009 · 12.1K citations · Full text
AUGUSTUS: ab initio prediction of alternative transcripts
Mario Stanke, O. Keller, Irfan Gunduz et al. · Nucleic Acids Research · 2006 · 3K citations · Full text
Using native and syntenically mapped cDNA alignments to improve <i>de novo</i> gene finding
Mario Stanke, Mark Diekhans, Robert Baertsch et al. · Bioinformatics · 2008 · 2.6K citations · Full text
1–5 of 302
2.1K
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National and Kapodistrian University of Athens, Greece
4 publications · 95 citations
4
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4
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4
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1–5 of 2.1K
640
Inserm
Paris, France
10 h-index
75 publications
5.2K citations

European Bioinformatics Institute
Cambridge, United Kingdom
10 h-index
46 publications
9K citations

Johns Hopkins University
Baltimore, United States
9 h-index
55 publications
4.2K citations

Johns Hopkins Medicine
Baltimore, United States
8 h-index
31 publications
1.8K citations

University of Toronto
Toronto, Canada
8 h-index
29 publications
5.3K citations
National Institutes of Health
Bethesda, United States
8 h-index
34 publications
3K citations

The University of Queensland
Brisbane, Australia
7 h-index
31 publications
3.3K citations
University of Michigan
Ann Arbor, United States
7 h-index
21 publications
1.4K citations
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34 publications · 8.4K citations
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19 publications · 15.7K citations
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14 publications · 827 citations
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11 publications · 612 citations
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11 publications · 852 citations
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