NGSEP/NGSEPcore
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).
JavaGPL-3.0
Stargazers
- alceballosa
- alejorojas2Michigan State University
- avinashkarnCornell University
- c4ts0upUniversidad de los Andes
- comeryBGI
- davidecarlson
- dcgerardAmerican University
- denise0593
- emricos
- ferrolad
- gastonlp
- hdescobarhNational University of Colombia
- helenwsungUniversity of Hawaii at Manoa
- kfuku52National Institute of Genetics
- llq0325
- LQHHHHHNanjing Agricultural University
- mariamadrid19Leuven, Belgium
- maypoleflynBeijing Agro-biotechnology Research Center
- nmacneilGraduate Student @ MUN
- pascalangstUniversity of Basel
- peterdfieldsUniversity of Basel
- qclian
- QinZhen1995
- Rem1burwell
- rgarcia11
- sardila13
- seb-muellerAlva Genomics
- SethMusker
- shanwai1234Fargo, ND
- shulp2211
- slemus947 Degrees
- steff456@Open-Craft
- TheOafidianUAntwerpen
- villegarUniversity of Liverpool | @groundswelluk
- waldeyrPresidência da República
- zuber-bioinfoIndia