Karyosoft - Version Variants - Software for Mutation Discovery Made Easy
Easy to use with just a few clicks and web-based. Flexibility to use single or multiple samples. 41 to 168 days saving for 96 samples. A simple report for whole-genome variant distribution. All your genomic variants information at your fingertips.
How do I use it?
- Open Variants on any browser
- Upload the reference genome data and gff of your interest
- Upload the raw data of your sample(s) of interest
- Follow the workflow by just clicking three buttons
- Get the results in 4 hours per 4 samples
What all do I get?
- A full report of whole-genome variant distribution.
- Annotations include genes, effect, regions, and more.
- Easy download of SNPs and In-dels with annotation and intermediate files such as indexed reference, samples, BAM files and more for other downstream applications.
- Integrated quality report of your fastq data.
What do I use it for?
- Mutation discovery for the traits of your interest
- Custom chip with desired variants for genotyping
- Direct genotyping of your population
- Flexibility to trace back the workflow steps at any time
- Correlating variants with phenotypes