Event box

This training will provide an introduction to exome sequencing data analysis followed by tutorials showing the use of exome analysis workflow and preparing participants to independently run basic exome analysis for variant detection using a “point and click” approach on a public Galaxy platform.

The hands-on exercise will run on a Galaxy platform using Illumina paired-end exome sequencing data. Participants will have a chance to:

1. Run quality control check on sequencing data
2. Align the sequencing reads to a reference genome
3. Generate alignment statistics and check mapping quality
4. Identify variants
5. Visualize the exome sequencing data and variants

To register for this in-person fill out the form below.

10:00am - 4:00pm
Training Room
NIH Library
Bioinformatics Curriculum
Registration has closed.

Event Organizer

Medha Bhagwat