I would like to suggest a section of courses!
1. Welcome and Introduction to the Course
Eric Green, M.D., Ph.D.
Director, National Human Genome Research Institute
2. Whole-Exome Sequencing: Technical Details
James Mullikin, Ph.D.
Director, NIH Intramural Sequencing Center
Mullikin Citations
3. Variant Annotation and Viewing Exome Sequencing Data
Jamie K. Teer, Ph.D.
Genetic Disease Research Branch, NHGRI
Teer Citations
4. Filtering Strategies for Identifying Germline Variants that Cause Disease
Leslie Biesecker, M.D.
Chief, Genetic Disease Research Branch, NHGRI
Biesecker Citations
5. Whole-Exome Sequencing to Identify Somatic Variants in Cancer
Yardena Samuels, Ph.D.
Cancer Genetics Branch, NHGRI
Samuels Citations
6. Morning Speakers Q&A Panel
7. Integrating Exome Variants with Other Genomic Data and Functional Annotations
David Adams, M.D., Ph.D.
Medical Genetics Branch, NHGRI
8. Secondary or Incidental Findings from Exome Sequence Data
Jennifer Johnston, Ph.D.
Genetic Disease Research Branch, NHGRI
Johnston Citations
9. Ethics and IRB Issues Related to Whole-Exome Sequencing
Sara Hull, Ph.D.
NHGRI and Department of Bioethics, NIH Clinical Center
Hull Citations
10. Informed Consent and Returning Results in Whole-Exome Sequencing Protocols
Julie Sapp, Sc.M., C.G.C.
Genetic Disease Research Branch, NHGRI
Sapp Citations
11. Afternoon Speakers Q&A Panel
