ロード中...

A new tool for prioritization of sequence variants from whole exome sequencing data

BACKGROUND: Whole exome sequencing (WES) has provided a means for researchers to gain access to a highly enriched subset of the human genome in which to search for variants that are likely to be pathogenic and possibly provide important insights into disease mechanisms. In developing countries, bioi...

詳細記述

保存先:
書誌詳細
出版年:Source Code Biol Med
主要な著者: Glanzmann, Brigitte, Herbst, Hendri, Kinnear, Craig J., Möller, Marlo, Gamieldien, Junaid, Bardien, Soraya
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4929716/
https://ncbi.nlm.nih.gov/pubmed/27375772
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13029-016-0056-8
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!