When:
Wednesday, December 7, 2016
11:30 AM - 1:00 PM CT
Where: Ward Building, Galter Library, Learning Resources Center, 303 E. Chicago Avenue, Chicago, IL 60611 map it
Audience: Faculty/Staff - Student - Post Docs/Docs - Graduate Students
Cost: Free
Contact:
Melanie Wilson
Group: Northwestern Information Technology
Category: Training
Following quality control, alignment of sequence reads to a reference genome (or generating a de novo assembly) is one of the first steps of sequence data analysis. This session will provide details and recommendations on tools and techniques for sequence read alignment and visualization of the aligned reads against a reference genome.
Users are encouraged to bring laptops to this session.