Course Details

  • Date: April 10th, 2019 - April 10th, 2019
  • Time: 9:00 am - 11:00 am
  • Location: Auditorium, Bldg. 549, Ft. Detrick
  • Presenter(s):
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