NGSEP is an integrated framework for analysis of high throughput sequencing (HTS) reads. The main functionality of NGSEP is the variants detector, which allows to make integrated discovery and genotyping of Single Nucleotide Variants (SNVs), insertions, deletions, and genomic regions with copy number variation (CNVs).
Added a workaround for CORS policies that wouldn't let the .html file access the .tsv files. Everything is now on a javascript file, on separate javascript objects.
Added a workaround for CORS policies that wouldn't let the .html file access the .tsv files. Everything is now on a javascript file, on separate javascript objects.