Seeing beyond the target: Leveraging off-target reads in targeted clinical tumor sequencing to identify prognostic biomarkers
Serghei ManguliD, Jaqueline BritoiD, Stefan GrohaiD, Noah ZaitleniD, Alexander GuseviD
Abstract
Clinical tumor sequencing is rapidly becoming a standard component of clinical care, providing essential information for selecting amongst treatment options and providing prognostic value. Here we develop a robust and scalable software platform (SBT: Seeing Beyond the Target) that mines discarded components of clinical sequences to produce estimates of a rich set of omics features including rDNA and mtDNA copy number, microbial species abundance, and T and B cell receptor sequences. We validate the accuracy of SBT via comparison to multimodal data from the TCGA and apply SBT to a tumor panel cohort of 2,920 lung adenocarcinomas to identify associations of clinical value. We replicated known associations of somatic events in TP53 with changes in rDNA (p=0.012); as well as diversity of BCR and TCR repertoires with the biopsy site (p=2.5x10-6, p<10-20). We observed striking differences in EGFR mutant lung cancers versus wild-type, including higher rDNA copy number and lower immune repertoire diversity. Integrating clinical outcomes, we identified significant prognostic associations with overall survival, including SBT estimates of 5S rDNA (p=1.9x10-4, hazard ratio = 1.22) and TCR diversity (p=2.7x10-3, hazard ratio=1.77). Both novel survival associations replicated in 1,302 breast carcinoma and 1,651 colorectal cancer tumors. We anticipate that feature estimates derived by SBT will yield novel biomarker hypotheses and open research opportunities in existing and emerging clinical tumor sequencing cohorts.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 4
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Estimating tumor mutational burden from RNA-sequencing without a matched-normal sample
Rotem Katzir, Noam Rudberg, Keren Yizhak·Nature CommunicationsPeer-reviewed·Jun 2, 2022
- Integrated Multi-Omics Analysis for the Identification of Disease-Associated Variations and Prognostic Biomarkers in Triple-Negative Breast Cancer (TNBC)
NAGENDRA MANNEKUNTA, Elamathi Natarajan·bioRxiv·May 29, 2026
- Restriction site associated DNA sequencing for tumour mutation burden estimation and mutation signature analysis
Conor McGuinness, Michael A. Black, Anita K. Dunbier·Cancer MedicinePeer-reviewed·Nov 17, 2023
- Use of an integrated pan-cancer oncology enrichment NGS assay to measure tumour mutational burden and detect clinically actionable variants
Valerie Pestinger, Matthew Ryan Smith, … Andrew David Beggs·Molecular Diagnosis & TherapyPeer-reviewed·Apr 18, 2020
- OncoRep: An n-of-1 reporting tool to support genome-guided treatment for breast cancer patients using RNA-sequencing
Tobias Meißner, Kathleen M. Fisch, … Andrew I. Su·bioRxiv·Sep 3, 2014
- The Mutational Landscape of the SCAN-B Real-World Primary Breast Cancer Transcriptome
C. Brueffer, S. Gladchuk, … L. H. Saal·bioRxiv·Jan 30, 2020