https://doi.org/10.7490/f1000research.1117641.1
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Oliver GR, Tang X, Schultz-Rogers LE et al. A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease [version 1; not peer reviewed]. F1000Research 2019, 8:1906 (poster) (https://doi.org/10.7490/f1000research.1117641.1)
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A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease

Gavin R. Oliver1, Xiaojia Tang, Laura E. Schultz-Rogers, Noemi Vidal-Folch, W. Garrett Jenkinson, Tanya L. Schwab, Krutika Gaonkar, Margot A. Cousin, Asha Nair, Shubham Basu, Pritha Chanana, Devin Oglesbee, Eric W. Klee
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Published 11 Nov 2019

A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease

[version 1; not peer reviewed]

Gavin R. Oliver1, Xiaojia Tang, Laura E. Schultz-Rogers, Noemi Vidal-Folch, W. Garrett Jenkinson, Tanya L. Schwab, Krutika Gaonkar, Margot A. Cousin, Asha Nair, Shubham Basu, Pritha Chanana, Devin Oglesbee, Eric W. Klee
Author Affiliations
1 Mayo Clinic in Rochester, USA
Presented at
Genome Informatics 2019
Abstract
Competing Interests

No competing interests were disclosed

Keywords
fusion transcript, fusion, inherited disease, mendelian disease, diagnostic odyssey
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