Expanded carrier screening in an infertile/affected Couple for determining carrier status for genetic mutations - VarSeq Couple carrier Workflow
Presented By: Dr. Muthukumaran, Team Lead, Clinical Bioinformatician, Anderson Diagnostics & Lab
VarSeq proves to be an invaluable asset for biologists, geneticists, researchers, and bioinformaticians by streamlining the process of filtering thousands of variants down to a critical few through its filtering cascade and information tracks. Please enjoy this webcast recording. Should you have any questions about the content covered, please reach out to our team here. Popular Products SNP & Variation Suite is a powerful analytic tool that allows biologists and other researchers to easily perform complex analyses and visualizations on genomic and phenotypic data. VarSeq is an intuitive, integrated software solution for tertiary analysis. With VarSeq you can automate your workflows and analyze variants for gene panels, exomes, and whole genomes. Built on the same algorithms of Varseq, VSWarehouse is a scalable, multi-project warehouse for NGS variant call sets, clinical reports, and catalogs of variant assessments.
In this presentation, Dr. Muthukumaran dives into the integral role VarSeq plays in Expanded Carrier Screening among infertile or affected Couople for determining carrier status for genetic mutations.
Watch as Dr. Muthukumaran discusses and displays the VarSeq Couple carrier workflow.
Watch on demand
