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

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...

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Bibliographic Details
Main Authors: In-Pyo Baek, Yong-Bok Jeong, Seung-Hyun Jung, Yeun-Jun Chung
Format: Article
Language:English
Published: BioMed Central 2014-12-01
Series:Genomics & Informatics
Subjects:
cancer
mutation
next-generation sequencing (NGS)
sequence snalysis
single-nucleotide variant (SNV)
software
Online Access:http://genominfo.org/upload/pdf/gni-12-289.pdf
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http://genominfo.org/upload/pdf/gni-12-289.pdf

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