Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux
Cancer genomics is a rapidly evolving field that utilizes next-generation sequencing (NGS) technologies to better understand the genetic basis of
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Cancer genomics
Cancer data brings its own problems: tumour heterogeneity and somatic variants and matched normals. These courses run exome and genome pipelines built for that.
- 2courses
- 86video lessons
- $149.99cheapest paid course
- $21.74a month for everything
What you will learn here
- Somatic variant calling
- Tumour and normal comparisons
- Exome workflows for cancer
- Whole genome workflows
- Variant annotation
- Interpreting cancer variants
Who takes these courses. Researchers working on tumour sequencing data.
The courses
Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux
In the field of cancer genomics, the analysis of NGS/whole genome data has become an integral part of cancer research.
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