ncibtep@nih.gov

Bioinformatics Training and Education Program

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

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

 When: Oct. 26th, 2018 9:00 am - 11:00 am

This class has ended.
Video Archive *Class recordings may take ~48 hours to become available.
To Know
  • Where: Rm 6041, NIH Bldg 37, Rm 6107
  • Organized By: BTEP
  • Files

About this Class

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

Files

  • BTEP_26thOct_update.pptx: |