Key Benefits

​​

• Easy to use with just a few clicks and web-based

 

• Cost-effective

 

• A secured permanent repository for all your SNP and In-del variants either on-premise or any cloud servers

 

• A simple report for whole-genome variant distribution

 

• All your genomic variants information at your fingertips

What all do I get?

​​

• A comprehensive Variant report across all genomic regions for your publication

 

• Annotations include genes, effect, regions, and more   

 

• All SNP and In-del variants across 

 

• A user-friendly database to manage and mine all your millions of variants at anytime and anywhere

How do I use it?

​​

• Open variant calling software on any browser

 

• Upload the reference genome sequences of your interest

​

• Upload the raw data of your sample(s) of interest

 

• Follow the workflow by just clicking a few buttons 

​

• Get the comprehensive variant report and all variants

​

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​