| 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
