<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kather JN</submitter><funding>NIDCR NIH HHS</funding><funding>European Research Council</funding><funding>NCI NIH HHS</funding><pagination>789-799</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7610412</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>1(8)</volume><pubmed_abstract>Molecular alterations in cancer can cause phenotypic changes in tumor cells and their micro-environment. Routine histopathology tissue slides - which are ubiquitously available - can reflect such morphological changes. Here, we show that deep learning can consistently infer a wide range of genetic mutations, molecular tumor subtypes, gene expression signatures and standard pathology biomarkers directly from routine histology. We developed, optimized, validated and publicly released a one-stop-shop workflow and applied it to tissue slides of more than 5000 patients across multiple solid tumors. Our findings show that a single deep learning algorithm can be trained to predict a wide range of molecular alterations from routine, paraffin-embedded histology slides stained with hematoxylin and e</pubmed_abstract><journal>Nature cancer</journal><pubmed_title>Pan-cancer image-based detection of clinically actionable genetic alterations.</pubmed_title><pmcid>PMC7610412</pmcid><funding_grant_id>771083</funding_grant_id><funding_grant_id>K08 DE026500</funding_grant_id><funding_grant_id>208237</funding_grant_id><funding_grant_id>P30 CA014599</funding_grant_id><pubmed_authors>Kochanny S</pubmed_authors><pubmed_authors>Kather JN</pubmed_authors><pubmed_authors>Trautwein C</pubmed_authors><pubmed_authors>Speirs V</pubmed_authors><pubmed_authors>Ortiz-Bruchle NN</pubmed_authors><pubmed_authors>Sommer KAJ</pubmed_authors><pubmed_authors>Pearson AT</pubmed_authors><pubmed_authors>Buelow RD</pubmed_authors><pubmed_authors>Srisuwananukorn A</pubmed_authors><pubmed_authors>Grabsch HI</pubmed_authors><pubmed_authors>Krause J</pubmed_authors><pubmed_authors>Loeffler C</pubmed_authors><pubmed_authors>Luedde T</pubmed_authors><pubmed_authors>Bankhead P</pubmed_authors><pubmed_authors>Hanby AM</pubmed_authors><pubmed_authors>Niehues JM</pubmed_authors><pubmed_authors>van den Brandt PA</pubmed_authors><pubmed_authors>Echle A</pubmed_authors><pubmed_authors>Jager D</pubmed_authors><pubmed_authors>Boor P</pubmed_authors><pubmed_authors>Schulte JJ</pubmed_authors><pubmed_authors>Muti HS</pubmed_authors><pubmed_authors>Brenner H</pubmed_authors><pubmed_authors>Heij LR</pubmed_authors><pubmed_authors>Cipriani NA</pubmed_authors><pubmed_authors>Kooreman LFS</pubmed_authors><pubmed_authors>Patnaik A</pubmed_authors><pubmed_authors>Hoffmeister M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pan-cancer image-based detection of clinically actionable genetic alterations.</name><description>Molecular alterations in cancer can cause phenotypic changes in tumor cells and their micro-environment. Routine histopathology tissue slides - which are ubiquitously available - can reflect such morphological changes. Here, we show that deep learning can consistently infer a wide range of genetic mutations, molecular tumor subtypes, gene expression signatures and standard pathology biomarkers directly from routine histology. We developed, optimized, validated and publicly released a one-stop-shop workflow and applied it to tissue slides of more than 5000 patients across multiple solid tumors. Our findings show that a single deep learning algorithm can be trained to predict a wide range of molecular alterations from routine, paraffin-embedded histology slides stained with hematoxylin and e</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2026-06-02T18:32:49.806Z</modification><creation>2025-04-06T18:04:44.579Z</creation></dates><accession>S-EPMC7610412</accession><cross_references><pubmed>33763651</pubmed><doi>10.1038/s43018-020-0087-6</doi></cross_references></HashMap>