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SnpReportR: A Tool for Clinical Reporting of RNAseq Expression and Variants
preprintposted on 16.09.2021, 21:11 by Ahmad Al Khleifat, Jenny Leopoldina Smith, Brandon M. Blobner, Sierra D. Miller, Kymberleigh Pagel, Annie Nadkarni, Melanie GaineyMelanie Gainey, Patrick CampbellPatrick Campbell, Olaitan I. Awe, Manuel Belmadani, Alan M. Cleary, Nicholas P. Cooley, Shamika Dhuri, Virginie Grosboillot, Brian Haas, Samuel Hokin, Ekaterina Orlova, Meghana Pagadala, Stephen Price, Adelaide Rhodes, Janice Kyla Nascimento Smith, Chaitanya Srinivasan, Barry Zorman, Ben Busby
In January 2021, four teams of scientists, clinicians, and developers from around the world worked collaboratively in a virtual hackathon to create a framework for the automated analysis and interpretation of RNA sequencing data in the clinic. This preprint in BioHackrXiv describes SnpReportR: A Tool for Clinical Reporting of RNAseq Expression and Variants aimed for use by clinicians and others without in-depth knowledge of genetics.