Complete Genomics Webinar Series

Join us for three webinars in December

First learn how our new cancer service can addresses the challenges associated with sequencing cancer samples.  Two additional webinars will discuss common analysis workflows used by our customers.

1 - New Cancer Sequencing Service

2 - Case-Control Analysis Workflow

3 - Family-Based Analysis Workflow

1 - New Cancer Sequencing Service

In this 30-minute webinar, learn how our unique cancer sequencing service provides the most comprehensive reporting of somatic and germline variants across the human genome.  Hear how Complete Genomics has addressed the challenges associated with cancer samples. Find out the details on the advancements to our bioinformatics pipeline and see data and results from our new cancer sequencing service.

Speaker: Sharoni Jacobs, PhD, Senior Product Manager, Complete Genomics

Date: Thursday, December 8th

Time: 8 am PST

Register now!

2 - Case-Control Analysis Workflow

Case-control studies are an important part of statistically significant sequencing studies. One key factor is proper experimental design, and to accomplish this effectively, analytical methods must be robust/impressive enough to detect low frequency variants. In this 30-minute webinar, hear about case-control analysis and how you can apply it to your research study.

Speaker: Jason Laramie, PhD, Principal Applications Scientist, Complete Genomics

Date: Wednesday, December 14th - NOTE change in date!

Time: 8 am PST

Register now!

3 - Family-Based Analysis Workflow

The use of family-based association studies offers the advantage of having a common genetic background from which to infer/discover variant information. In this 30-minute webinar, learn how to design and perform family-bases analyses and identify causative variants from whole genome data.

Speaker: Rick Tearle, PhD, Senior Applications Scientist, Complete Genomics

Date: Thursday, December 15th

Time: 8 am PST

Register now!