MAP: Mutation Arranger for Defining Phenotype-Related Single-Nucleotide Variant

Next-generation sequencing (NGS) is widely used to identify the causative mutations underlying diverse human diseases, including cancers, which can be useful for discovering the diagnostic and therapeutic targets. Currently, a number of single-nucleotide variant (SNV)-calling algorithms are availabl...

詳細記述

書誌詳細

主要な著者:	In-Pyo Baek, Yong-Bok Jeong, Seung-Hyun Jung, Yeun-Jun Chung
フォーマット:	Artigo
言語:	Inglês
出版事項:	BioMed Central 2014-12-01
シリーズ:	Genomics & Informatics
主題:	cancer mutation next-generation sequencing (NGS) sequence snalysis single-nucleotide variant (SNV) software
オンライン･アクセス:	http://genominfo.org/upload/pdf/gni-12-289.pdf
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