BTEP, Frederick: Variant Analysis: SNVs, CNVs and Structural Variants in WGS and WES – CANCELLED

THIS EVENT HAS BEEN CANCELLED
10x Genomics: Whole Exome and Whole Genome Analysis

• How 10x Genomics linked reads works
• SNVs, copy number variations, structural variants and phasing of the variants from linked read data
• Walk through of 10x Genomics WGS results
• Integration of linked reads data with other platforms/technologies

All Structural Variants:

• CCR Sequencing Facility analysis pipelines of structural variants from Illumina, linked reads, long reads and optical mapping
• Walk through of SV/CNV pipelines, how they work and results from the SV pipelines