NGSAP-VC : Genomic Variant Calling as an Installable GALAXY Workflow Using NGS data.

Implementation of genomic variants calling as an installable GALAXY workflows using NGS data. Repository contains two separate sets of simulated ebola test data. One for SNPs and INDELs calling and another for Structural Variants calling.基于二代测序（Next-Generation Sequencing, NGS）数据实现可部署的Galaxy工作流以完成基因组变异检测。本代码存储库包含两套独立的模拟埃博拉病毒检测数据集，其中一套用于单核苷酸多态性（Single Nucleotide Polymorphisms, SNPs）与插入缺失变异（insertions-deletions, INDELs）检测，另一套用于结构变异（Structural Variants）检测。