Course Details

  • Date: October 26th, 2018 - October 26th, 2018
  • Time: 9:00 am - 11:00 am
  • Location: NIH Bldg 37, Rm 6041, Rm 6107
  • Presenter(s):
  • Course Number: 1007

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

Course Material 1:  BTEP_26thOct_update.pptx