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PMID: 24681721 Published · ppublish English Letter Research Support, Non-U.S. Gov't

MutationTaster2: mutation prediction for the deep-sequencing age.

Nature methods ·Vol. 11 ·No. 4 ·2014-04-00 ·Pages 361-2

Schwarz JM, Cooper DN, Schuelke M, Seelow D

Abstract

暂无摘要

MeSH Terms
Base Sequence DNA/genetics DNA Barcoding, Taxonomic Mutation Software
Chemicals
DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schwarz Jana Marie
1] Department of Neuropediatrics, Charité - Universitätsmedizin Berlin, Berlin, Germany. [2] NeuroCure Clinical Research Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Cooper David N
Institute of Medical Genetics, Cardiff University, Cardiff, UK.
Schuelke Markus
1] Department of Neuropediatrics, Charité - Universitätsmedizin Berlin, Berlin, Germany. [2] NeuroCure Clinical Research Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Seelow Dominik
1] Department of Neuropediatrics, Charité - Universitätsmedizin Berlin, Berlin, Germany. [2] NeuroCure Clinical Research Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
References (8)
8 references, click to expand
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    PLoS One. 2008;3(12):e3874 PMID: 19057649
  7. ClinVar: public archive of relationships among sequence variation and human phenotype.
    Nucleic Acids Res. 2014 Jan;42(Database issue):D980-5 PMID: 24234437
  8. The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine.
    Hum Genet. 2014 Jan;133(1):1-9 PMID: 24077912
Article Info
Journal
Nature methods
Abbr.
Nat Methods
ISSN
1548-7105
DOI
10.1038/nmeth.2890
Published
2014-04-00
Pages
361-2
Language
English
Region
United States
NLM ID
101215604
Subset
IM
External Links
PubMed source DOI: 10.1038/nmeth.2890 View journal details
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