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Analyzing Short/Long read sequencing results and interpreting splicing events.
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.
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.
Answered on April 1st, 2021 by email@example.com