File(s) stored somewhere else

Please note: Linked content is NOT stored on Carnegie Mellon University and we can't guarantee its availability, quality, security or accept any liability.

SnpReportR: A Tool for Clinical Reporting of RNAseq Expression and Variants

preprint
posted 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.

History

Date

29/06/2021

Usage metrics

Categories

Licence

Exports