In this 2-hour workshop, you will have hands-on experience on SNV calling and analysis. You will be provided toy short-read sequencing samples, followed by read alignments, variant calling and pathogenicity analysis.
This workshop will guide you through the workflow of a simple genomic SNV analysis.
This is a hands-on workshop, which means you will be given time to get the tools running.
For each task, you will be given a brief instruction prior to getting your hands dirty. At the end of the given time, there will be a brief summary.
Basic knowledge of using command line and Rstudio is ideal. Although strictly speaking, no prior knowledge is required to attend this workshop.
The workshop runs for 2 hours. You will find tasks and related information in the worksheet.
If you run into any problems, please describe the issue and send via zoom chat. The instructors will be monitoring the chat panel and answer any question in real time.
For this 120-minute workshop:
| Activity | Time |
|---|---|
| Introduction | 5m |
| Working Environment: command line and Rstudio | 15m |
| Read Alignment: bwa and samtools | 20m |
| SNV calling: Strelka2 | 20m |
| Pathogenicity analysis | 50m |
| Summary | 10m |
Variant calling is a vital component of genomics studies. Genomic variants have been found in various structures and sizes, including single-nucleotide variants (SNVs), small insertion and deletions (INDELs), copy number variants (CNVs) and structural variants (SVs). Computational tools for detecting these variants are developed with different underlying approaches.
This workshop is designed to offer a hands-on experience on genomic variant calling and analysis. The tasks are designed to guide you through the key steps of SNV analysis on a tumour/normal paired sample.