ncibtep@nih.gov

Bioinformatics Training and Education Program

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

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

 When: Apr. 10th, 2019 9:00 am - 11:00 am

To Know

Where:
Ft. Detrick, Bldg. 549, Auditorium
Organizer:
BTEP
This class has ended.
Video Archive *Class recordings may take ~48 hours to become available.

About this Class

BTEP
Wednesday, April 10, 2019
9:00 am  |  Eastern Daylight Time (New York, GMT-04:00)  |  2 hrs
Meeting number (access code): 738 427 711
Meeting password: zPJpWP$6
    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