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...
| Main Authors: | , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Korea Genome Organization
2014
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330268/ |