In this webinar, you will learn about the latest bioinformatics analysis tools for analyzing DNA-Seq data, including practical applications for identifying and interpreting candidate functional variants. We will take a closer look at VarSeq, a DNA-seq analysis tool offered by Golden Helix. Topics covered will include: Rare variant analysis and prioritization with cancer gene panels, single exomes and exome trios. We will also cover visualization of VCF & BAM files in GenomeBrowse. Dr. Ahmed Alfares will kick off the event with a look at his VarSeq workflow used at Qassim University Hospital for analyzing consanguine family data. Hauwa Yusuf from Golden Helix will then present an in-depth overview of VarSeq showcasing analysis workflows, data visualization, and available clinical reporting options.

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