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

 

Speaker: Keyur Talsania, Bioinformatics Analyst, CCR-SF IFX Group

Date: Oct. 26, 2018

Time: 9 – 11 AM

Location: NIH Bldg. 37, Rm. 6041/6107

Categories: Uncategorized