MAP: Mutation Arranger for Defining Phenotype-Related Single-Nucleotide Variant
نویسندگان
چکیده
منابع مشابه
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 available; however, there is no tool for visualizing the recurrent and phenotype-specific mutations for g...
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ژورنال
عنوان ژورنال: Genomics & Informatics
سال: 2014
ISSN: 2234-0742
DOI: 10.5808/gi.2014.12.4.289