<p>A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease</p>

Gavin R. Oliver; 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

doi: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 A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease [version 1; not peer reviewed].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

Published 11 Nov 2019 (https://doi.org/10.7490/f1000research.1117641.1)

Author Affiliations

¹ Mayo Clinic in Rochester, USA

Copyright © 2019 Oliver GR et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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CITE

Published 11 Nov 2019

A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease
[version 1; not peer reviewed]

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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