Dear Scientist:
The Bioinformatics Training and Education Program (BTEP) is pleased to present
a workshop on “Variant Analysis: SNVs, CNVs and Structural Variants in WGS and
WES”.
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
Date: October 26, 2018
Time: 9 AM - 11 AM
Location: NIH, Bldg 37, Rm 6041/6107
Presenter(s): Keyur Talsania, NCI-SF IFX Group
Registration is required:
https://btep.ccr.cancer.gov/classes/btep-analysis-snv-cnv-structural-variants-wgs-wes
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Visit the BTEP website:
https://btep.ccr.cancer.gov<https://btep.ccr.cancer.gov/>
Questions/Comments and/or suggestions may be directed to:
[email protected]<mailto:[email protected]>
Dr. Amy Stonelake 240-760-6314
Dr. Peter FitzGerald 240-760-7181
Amy Stonelake, Ph.D. [Contractor]
Scientific Manager, Bioinformatics Training & Education Program (BTEP)
Leidos Biomedical Research
Frederick National Laboratory for Cancer Research
Email: [email protected]<mailto:[email protected]>
Phone: (240) 760-6314
Location: NIH, Bldg 37, Rm 3035
