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Karyosoft -Model Variants -Software for Mutation Discovery Made Easy

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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.

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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