BTEP, Frederick: Variant Analysis: SNVs, CNVs and Structural Variants in WGS and WES
When: Apr. 10th, 2019 9:00 am - 11:00 am
This class has ended.
Video Archive
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To Know
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Where: Ft. Detrick, Bldg. 549, Auditorium
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Organized By: BTEP
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