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
Autores principales: Baek, In-Pyo, Jeong, Yong-Bok, Jung, Seung-Hyun, Chung, Yeun-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2014
Materias:
Application Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330268/
https://www.ncbi.nlm.nih.gov/pubmed/25705172
http://dx.doi.org/10.5808/GI.2014.12.4.289

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330268/
https://www.ncbi.nlm.nih.gov/pubmed/25705172
http://dx.doi.org/10.5808/GI.2014.12.4.289

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