Making Sense of Genomic Variation: Part 2 Structural Variants (RESCHEDULED)
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Making Sense of Genomic Variation: Part 2 Structural Variants (RESCHEDULED) In-Person
Structural variation encompasses diverse types of genomic variants including deletions, duplications, inversions, transpositions, translocations, among others. In many cases, determining whether a particular genetic variant is pathogenic or benign and its correlation with respect to a patient's disease phenotype is challenging.
In this session we use online resources and tools to find, retrieve, annotate, and visualize structural variants
- NCBI’s database of genomic structural variants dbVar
- Database ofDatabasE of Chromosomal Imbalance and Phenotype in Humans
- Genomic Variants DGVa
- UCSC and Ensembl genome browsers
- Date:
- Thursday, October 6, 2016
- Time:
- 11:00am - 12:30pm
- Time Zone:
- Eastern Time - US & Canada (change)
- Location:
- SHM L 101A, Simbonis Conference Room, Cushing/Whitney Medical Library, 333 Cedar St
- Campus:
- Medical School
- Categories:
- Bioinformatics
Registration has closed.
Event Organizer
Rolando Garcia-Milian
