Variant Analysis
Variations in nucleotide sequence, in the form of single nucleotide variants (SNVs) and insertion and deletion events (INDELs), can either be neutral in nature or can have functional effects. Partek Flow provides all the tools necessary to interrogate and prioritize variants for further analysis. Variants stored in Variant Call Format (vcf) files can be analyzed to filter, annotate, summarize, visualize, and validate your panel of identified variants. Multiple vcf processing tools are available under the Variant analysis section of the context sensitive menu
Additional Assistance
If you need additional assistance, please visit our support page to submit a help ticket or find phone numbers for regional support.
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