Pengfei Liu will present on anoverworkflow forrare disease diagnostics using RNA-seq.The workflow leverages patient cell transdifferentiation into induced neurons to improve molecular diagnostic yield of neurological genetic disorders。

This webinar series will describe responsible and meaningful community engagement approaches across the research lifecycle，ina manner that addresses health inequalities，avoids potential harms，builds trustworthy relationships，and increases the representation of underrepresented comnimuties and netis。

Dr.Appelbaum will discuss findings from a series of focus groups with patients，clinicians，and IRB members on return of polygenic risk scores in research.Despite strong interest in such results，they found multiple barriers to their effective use to improve health。

Dr.Gabrielle Lemire will discuss exome copy number variant（CNV）detection，analysis and classification on a cohort of 6633 families with undiagnosed rare genetic disorders.With the resolution provided by exome sequencing，they identified a causative CNV in2.6%of families and assessed CNV pathogenicityby applying an advanced classification approach。

This workshop is intended for anybody interested in learning CRISPR-based technologies。

This workshop will showcase new data types and new features of the UCSC Genome Browser。

The goal of this session will be to review the process of developing and submitting trainee grants。

Hear from leaders on an appropriate framework for the use of germline genome editing。