Qiagen CLC Genomics Workbench: De Novo Assembly Using Long Reads and Short Read Polishing
When: Jul. 18th, 2024 1:00 pm - 2:30 pm
Learning Level: Beginner
To Know
About this Class
Long read sequencing holds an advantage over short read sequencing in areas such as structural variant and transcript isoform discovery. This class will demonstrate long read analysis using Qiagen’s CLC Genomics Workbench, a point-and-click software for analyzing multi-omics sequencing data including RNA and ChIP. 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 reach out to the NIH Library (https://www.nihlibrary.nih.gov/resources/tools/clc-genomics-workbench) After this class, participants will be able to 1) perform de novo assembly as well as map high-quality long reads to reference and 2) polish de novo assembly of poor-quality long reads using high-quality short reads. Experience using and installation of this software is not needed to attend.
Meeting link:
https://cbiit.webex.com/cbiit/j.php?MTID=mc5699a15ca783a3a62a9ce26be123337
Meeting number:
2319 610 3073
Password:
YbMHySw*425
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Dial 23196103073@cbiit.webex.com
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Access code: 2319 610 3073