Small Nucleotide Variant Analysis Using <scp>RNA</scp> Fusion Panel ( <scp>SMURF</scp> ): Making the Most of <scp>RNAseq</scp> Data in Solid Tumours
This analysis suggests that the variants in these genes can be confidently reported from RNA-Seq data obtained from an RNA-based fusion panel.
Authors
- Beena Kumar (ORCID: https://orcid.org/0000-0002-6622-1274)
- Noel Djitro (ORCID: https://orcid.org/0000-0001-8192-9636)
- Priscillia Siswara
- Peter A. Kaub (ORCID: https://orcid.org/0000-0001-9921-2318)
- Amit Kumar (ORCID: https://orcid.org/0000-0003-4771-0627)
- Bin Yuan (ORCID: https://orcid.org/0000-0002-9632-4573)
- Liyan Song
- Anna Fong Na Goh
- Pamela Htain
- Pranav Dorwal
- Patricia Pyrchla
- Robert Quach
- Julie Robin
- Broden Krause
- Suzanne Svobodova
Institutions
- Peter MacCallum Cancer Centre (AU)
- Monash Health (AU)
- Monash University (AU)
Publication Details
- Journal
- Journal of Clinical Laboratory Analysis
- Published
- 2026-01-13
- DOI
- https://doi.org/10.1002/jcla.70164
- Primary Topic
- Cancer Genomics and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00