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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Detalles Bibliográficos
Publicado en:Genomics Inform
Main Authors: Baek, In-Pyo, Jeong, Yong-Bok, Jung, Seung-Hyun, Chung, Yeun-Jun
Formato: Artigo
Idioma:Inglês
Publicado: Korea Genome Organization 2014
Assuntos:
Application Note
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4330268/
https://ncbi.nlm.nih.gov/pubmed/25705172
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2014.12.4.289
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