Analyzing ChIP sequencing data using Qiagen's CLC Genomics Workbench

About this Class

Qiagen CLC Genomics Workbench is a point-and-click bioinformatics software that runs on a personal computer and enables bulk RNA sequencing, ChIP sequencing, long reads, and variant analysis. NCI scientists can use CLC Genomics Workbench through the NCI institutional license, just submit a ticket with service.cancer.gov to get it installed on personal computer. Others at NIH can inquire with the NIH Library (https://www.nihlibrary.nih.gov/resources/tools/clc-genomics-workbench) about using this package.

This class will guide participants through a complete ChIP sequencing analysis workflow using CLC Genomics Workbench. At the end of the session, participants will know how to:
 
·      Import and prepare the raw sequencing data for analysis.
·      Map the reads to a reference genome.
·      Call peaks.
·      Visualize results.
·      Extract sequences within peak region.
 
Experience using CLC Genomics Workbench is not required for participation.
 
Meeting link:
https://cbiit.webex.com/cbiit/j.php?MTID=mc1865c293c813a1e3dfbb239518d370a 
Meeting number:
2319 733 9579
Password:
CHbX8Gwv3*2

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Dial 23197339579@cbiit.webex.com
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