Published October 4, 2018
| Version v5
Lesson
Open
Variant Calling Analysis
Description
Msc in Computational Biology of Universidad Politécnica de Madrid (UPM)
Course: Genomics Data Analysis and Visualization
Lesson 1: Read mapping and variant calling
This tutorial is designed to introduce the tools, data types and workflow of variant detection. We will align reads to the genome, look for differences between reads and reference genome sequence, and filter the detected genomic variation manually to understand the computational basis of variant calling.
Files
Lesson_2_variant_calling.pdf
Files
(233.3 MB)
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