Introduction to the bioinformatics of cancer: high-throughput sequencing of the genome, epigenome and transcriptome

author: Valentina Boeva, Institut Curie
published: Feb. 17, 2015,   recorded: September 2014,   views: 2104
Categories

Slides

Related Open Educational Resources

Related content

Report a problem or upload files

If you have found a problem with this lecture or would like to send us extra material, articles, exercises, etc., please use our ticket system to describe your request and upload the data.
Enter your e-mail into the 'Cc' field, and we will keep you updated with your request's status.
Lecture popularity: You need to login to cast your vote.
  Bibliography

Description

In this presentation, I will introduce bioinformatics approaches to study genetic, epigenetic and transcriptome variations in cancer. I demonstrate how we can analyze whole genome, exome sequencing and amplicon sequencing data in order to find small mutations, copy number changes and large structural variants in cancer DNA. I will talk about the analysis of RNA-seq and ChIP-seq data in cancer studies.

Link this page

Would you like to put a link to this lecture on your homepage?
Go ahead! Copy the HTML snippet !

Write your own review or comment:

make sure you have javascript enabled or clear this field: