Would someone with RAP experience working on annotating VCF files for loss-of-function variants be willing to connect and offer tips/advice? I am new to the field and am feeling rather overwhelmed!

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Hey all,   I am a graduate student at Queen's University and am beginning my thesis research using the RAP. While I have a background in biomedical and genomic computing I am finding defining the pipeline I need to create for my project a rather tricky task. I am looking to investigate the association between loss of function in specific genes and certain phenotypic outcomes.   Please reach out to me if you feel like you would want to connect!

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