Questions › Analyzing Short/Long read sequencing results and interpreting splicing events.
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owensvv@nih.gov asked 6 months ago

I am a post-bac in DCEG. I am using sequencing data to analyze functional consequences of Insilico discovered novel variants in our patient cohort. I’d like help in using software to analyze the sequencing data and splicing events.

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stonelakeak@nih.gov Staff answered 6 months ago

Hi Valencia,
Welcome to the Bioinformatics for Beginners Class – we are happy to have you here. We will be working with sequence data in this course. We’ll work with STAR- a splicing aware aligner that runs on Unix systems in the second part to this course.