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