Date: 20 - 21 November 2017

This two day course serves as the first in a larger two-part course in conjunction with our Exome Variants, Copy Number Calling, Variant Annotation and Reporting workshop in December 2017, as well as a standalone introduction to DNA-seq. Attendees will receive an introduction to next generation sequencing (NGS) platforms, data analysis and tools for data quality control, read alignment (mapping) and refinement using DNA-seq data. The course will conclude with a basic introduction to variant calling as a lead-in to the December workshop.

Keywords: DNA-seq, bioinformatics

Venue: College Court

City: Leicester

Region: Leicestershire

Country: United Kingdom

Postcode: LE2 3UF

Organizer: University of Leicester BBASH

Host institutions: University of Leicester

Target audience: Academics, postdocs, PhD students, Clinical Scientists

Event types:

  • Workshops and courses

Scientific topics: Genetics, Bioinformatics


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