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

BACKGROUND: RNA sequencing has been proposed as a means of increasing diagnostic rates in studies of undiagnosed rare inherited disease. Recent studies have reported diagnostic improvements in the range of 7.5–35% by profiling splicing, gene expression quantification and allele specific expression....

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Detalles Bibliográficos
Autores principales: Oliver, Gavin R., Tang, Xiaojia, Schultz-Rogers, Laura E., Vidal-Folch, Noemi, Jenkinson, W. Garrett, Schwab, Tanya L., Gaonkar, Krutika, Cousin, Margot A., Nair, Asha, Basu, Shubham, Chanana, Pritha, Oglesbee, Devin, Klee, Eric W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774566/
https://www.ncbi.nlm.nih.gov/pubmed/31577830
http://dx.doi.org/10.1371/journal.pone.0223337

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774566/
https://www.ncbi.nlm.nih.gov/pubmed/31577830
http://dx.doi.org/10.1371/journal.pone.0223337

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