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Deep Learning Model for Tumor Type Prediction using Targeted Clinical Genomic Sequencing Data.


ABSTRACT: Tumor type guides clinical treatment decisions in cancer, but histology-based diagnosis remains challenging. Genomic alterations are highly diagnostic of tumor type, and tumor type classifiers trained on genomic features have been explored, but the most accurate methods are not clinically feasible, relying on features derived from whole genome sequencing (WGS), or predicting across limited cancer types. We use genomic features from a dataset of 39,787 solid tumors sequenced using a clinical targeted cancer gene panel to develop Genome-Derived-Diagnosis Ensemble (GDD-ENS): a hyperparameter ensemble for classifying tumor type using deep neural networks. GDD-ENS achieves 93% accuracy for high-confidence predictions across 38 cancer types, rivalling performance of WGS-based methods. GDD-ENS can also guide diagnoses on rare type and cancers of unknown primary, and incorporate patient-specific clinical information for improved predictions. Overall, integrating GDD-ENS into prospective clinical sequencing workflows has enabled clinically-relevant tumor type predictions to guide treatment decisions in real time.

SUBMITTER: Darmofal M 

PROVIDER: S-EPMC10508812 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

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Deep Learning Model for Tumor Type Prediction using Targeted Clinical Genomic Sequencing Data.

Darmofal Madison M   Suman Shalabh S   Atwal Gurnit G   Chen Jie-Fu JF   Chang Jason C JC   Toomey Michael M   Vakiani Efsevia E   Varghese Anna M AM   Rema Anoop Balakrishnan AB   Syed Aijazuddin A   Schultz Nikolaus N   Berger Michael M   Morris Quaid Q  

medRxiv : the preprint server for health sciences 20230910


Tumor type guides clinical treatment decisions in cancer, but histology-based diagnosis remains challenging. Genomic alterations are highly diagnostic of tumor type, and tumor type classifiers trained on genomic features have been explored, but the most accurate methods are not clinically feasible, relying on features derived from whole genome sequencing (WGS), or predicting across limited cancer types. We use genomic features from a dataset of 39,787 solid tumors sequenced using a clinical targ  ...[more]

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