Lasergene Weekly: Supplement your variant analysis using VCF files


VCF files can be used to enhance a variety of variant analysis workflows. In this week’s video, learn how to use VCF files for SNP analysis in Lasergene Genomics Suite. Explore the contents of a VCF file and learn how to load VCF files into SeqMan NGen prior to assembly, analyze the variants in SeqMan Pro, and utilize VCF files for large multi-sample variant analysis projects in ArrayStar.