Variant effect predictions capture some aspects of deep mutational scanning experiments

Variant effect predictions capture some aspects of deep mutational scanning experiments

Abstract Background Deep mutational scanning (DMS) studies exploit the mutational landscape of sequence variation by systematically and comprehensively assaying the effect of single amino acid variants (SAVs; also referred to as missense mutations, or non-synonymous Single Nucleotide Variants – miss...

詳細記述

書誌詳細
主要な著者: Jonas Reeb, Theresa Wirth, Burkhard Rost
フォーマット: 論文
言語:English
出版事項: BMC 2020-03-01
シリーズ:BMC Bioinformatics
主題:
Sequence variation
Variant effect prediction
Deep mutational scanning
Non-synonymous sequence variant
Missense variant
Single nucleotide variant
オンライン･アクセス:http://link.springer.com/article/10.1186/s12859-020-3439-4

インターネット

http://link.springer.com/article/10.1186/s12859-020-3439-4

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