Abstract 1417: Bulk RNA-seq atlas guided annotation of tumor transcriptomes.

Abstract Single-cell RNA sequencing (scRNA-seq) enables high-resolution profiling of cellular heterogeneity, revealing novel transcriptomic states. However, many existing generative and foundational single-cell models are trained predominantly on non-neoplastic data, limiting their accuracy in cancer cell annotation. We present SPOTTER (Seed-guided Prediction Of Tumor Transcriptomes with Ensemble Recognition), a framework that integrates bulk RNA sequencing (bulk RNA-seq) cancer atlases with single-cell data. SPOTTER first classifies individual cells using an ensemble neural network classifier OTTER (Oncologic TranscripTome Expression Recognition), trained on the hierarchical RACCOON (Resolution-Adaptive Coarse-to-fine Clusters OptimizatiON) cancer atlas spanning over 15,000 pediatric and adult cancer samples. High-confidence seed labels are selected using a Gaussian mixture model (GMM) and Gini impurity-based filtering of OTTER scores to exclude low-quality cells with uncertain predictions. These labels are then propagated through scANVI (single-cell Annotation using Variational Inference) to achieve per-cell classifications. Across nine diverse pediatric and adult single-cell and single-nucleus cancer datasets, SPOTTER reliably assigned malignant cells to their expected tumor classes. In Ewing sarcoma samples with matched bulk RNA-seq and single-nucleus RNA-seq (snRNA-seq), SPOTTER recapitulated bulk RNA-seq-defined subtypes at single-cell resolution, distinguishing one subtype enriched for neuronal programs, including SYT1 and SOX6, and another with increased EWS-FLI1 fusion activity and elevated JAK1 signaling—consistent with subtypes previously identified by OTTER and RACCOON in bulk RNA-seq. By integrating bulk and single-cell analyses, SPOTTER enables characterization of tumor heterogeneity and supports identification of subtype-specific markers to reveal critical insights into the transcriptomic profile of a cancer. Citation Format: Timmy T. Wen, Dusan Pesic, Pedro L. Ballester, Josh Nash, Adam Shlien., . Bulk RNA-seq atlas guided annotation of tumor transcriptomes [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1417.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1417
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 1417: Bulk RNA-seq atlas guided annotation of tumor transcriptomes.

Timmy T. Wen, Pedro L. Ballester, Josh Nash, Dusan Pesic et al.
Cancer Research
Single-cell and spatial transcriptomics
article

Abstract 1417: Bulk RNA-seq atlas guided annotation of tumor transcriptomes.

Timmy T. Wen, Pedro L. Ballester, Josh Nash, Dusan Pesic, Adam Shlien
article en

Abstract

Abstract Single-cell RNA sequencing (scRNA-seq) enables high-resolution profiling of cellular heterogeneity, revealing novel transcriptomic states. However, many existing generative and foundational single-cell models are trained predominantly on non-neoplastic data, limiting their accuracy in cancer cell annotation. We present SPOTTER (Seed-guided Prediction Of Tumor Transcriptomes with Ensemble Recognition), a framework that integrates bulk RNA sequencing (bulk RNA-seq) cancer atlases with single-cell data. SPOTTER first classifies individual cells using an ensemble neural network classifier OTTER (Oncologic TranscripTome Expression Recognition), trained on the hierarchical RACCOON (Resolution-Adaptive Coarse-to-fine Clusters OptimizatiON) cancer atlas spanning over 15,000 pediatric and adult cancer samples. High-confidence seed labels are selected using a Gaussian mixture model (GMM) and Gini impurity-based filtering of OTTER scores to exclude low-quality cells with uncertain predictions. These labels are then propagated through scANVI (single-cell Annotation using Variational Inference) to achieve per-cell classifications. Across nine diverse pediatric and adult single-cell and single-nucleus cancer datasets, SPOTTER reliably assigned malignant cells to their expected tumor classes. In Ewing sarcoma samples with matched bulk RNA-seq and single-nucleus RNA-seq (snRNA-seq), SPOTTER recapitulated bulk RNA-seq-defined subtypes at single-cell resolution, distinguishing one subtype enriched for neuronal programs, including SYT1 and SOX6, and another with increased EWS-FLI1 fusion activity and elevated JAK1 signaling—consistent with subtypes previously identified by OTTER and RACCOON in bulk RNA-seq. By integrating bulk and single-cell analyses, SPOTTER enables characterization of tumor heterogeneity and supports identification of subtype-specific markers to reveal critical insights into the transcriptomic profile of a cancer. Citation Format: Timmy T. Wen, Dusan Pesic, Pedro L. Ballester, Josh Nash, Adam Shlien., . Bulk RNA-seq atlas guided annotation of tumor transcriptomes [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1417.

Cancer ResearchVol. 86(7_Supplement)
Hospital for Sick Children (CA)
Openalex Percentile: Top 7%
Single-cell and spatial transcriptomics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.