| Tuesday, October 13, 2015 @ 09:00 am EDT — Tuesday, October 13, 2015 @ 04:00 pm EDT | ||||
| NCI Frederick - Building 549 Library Training Room | ||||
| chenx3@mail.nih.gov | ||||
| Bioinformatics Hands-On Training: Whole Exome and Amplicon Panel NGS Sequence Analysis using the CLC BioMedical Genomics Workbench CLCBio Biomedical Workbench experts from Qiagen will conduct a training in the NIH Frederick campus. Please register by Friday, October 9 2015. Registration is limited to the capacity of the training room; if the response is overwhelming we shall schedule another session and registrants shall be accordingly informed. Trainees will have computers in the training room with the application setup. Agenda: 1. Basic Introduction to the software including reference data setup, NGS data import/export, screen elements and display setup. 2. Working with the integrated genome browser and tracks. 3. Mapping reads to reference sequences and variant calling, filtering, annotation and comparison tools. Copy number variants, Indel & Structural Variant analysis also. 4. Batch processing and Workflow automation. Ready-to-Run Workflows. 5. Introduction to Ingenuity Variant Analysis – Short list your candidates for causal variants. 6. Extended Q & A |
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