Abstract
In this work we describe IGV-plus, a software for next-generation sequencing (NGS) data analysis and visualization. It integrates de facto standard tools for the discovery of genetic mutations in genomic-wide association studies. We describe the software specification that led to the development of IGV-plus. Finally, we show how we integrate a single-nucleotide polymorphism (SNP) calling software of the genome analysis toolkit (GATK) in the genome browser integrative genomics viewer (IGV), in order to create a centralized platform, as a possible one-stop shop for biologists dealing with NGS data.
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