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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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014-12-01
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| Colecção: | Genomics & Informatics |
| Assuntos: | |
| Acesso em linha: | http://genominfo.org/upload/pdf/gni-12-289.pdf |
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