Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products
-
Updated
Oct 31, 2024 - JavaScript
Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products
A tool for analysis of genomic variants in human genomes.
A Node.js library for reading and filtering variant call data using streams
Integrated tool for prediction of potential neoantigens - A fork from our original publication @ neoanthill/neoANT-HILL
Slides for presentation to the Queensland Mycobacterium Reference Laboratory 24/02/2022
Add a description, image, and links to the variant-calling topic page so that developers can more easily learn about it.
To associate your repository with the variant-calling topic, visit your repo's landing page and select "manage topics."