<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vaske OM</submitter><funding>Howard Hughes Medical Institute</funding><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>e1913968</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6822083</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(10)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>Pediatric cancers are epigenetic diseases; therefore, considering tumor gene expression information is necessary for a complete understanding of the tumorigenic processes.&lt;h4>Objective&lt;/h4>To evaluate the feasibility and utility of incorporating comparative gene expression information into the precision medicine framework for difficult-to-treat pediatric and young adult patients with cancer.&lt;h4>Design, setting, and participants&lt;/h4>This cohort study was conducted as a consortium between the University of California, Santa Cruz (UCSC) Treehouse Childhood Cancer Initiative and clinical genomic trials. RNA sequencing (RNA-Seq) data were obtained from the following 4 clinical sites and analyzed at UCSC: British Columbia Children's Hospital (n = 31), Lucile Packard Children's</pubmed_abstract><journal>JAMA network open</journal><pubmed_title>Comparative Tumor RNA Sequencing Analysis for Difficult-to-Treat Pediatric and Young Adult Patients With Cancer.</pubmed_title><pmcid>PMC6822083</pmcid><funding_grant_id>U24 CA210974</funding_grant_id><funding_grant_id>U24 CA195858</funding_grant_id><funding_grant_id>T32 HG008345</funding_grant_id><funding_grant_id>U24 CA180951</funding_grant_id><pubmed_authors>Durbin A</pubmed_authors><pubmed_authors>McColl D</pubmed_authors><pubmed_authors>Beale H</pubmed_authors><pubmed_authors>Byron SA</pubmed_authors><pubmed_authors>Tayi Shah A</pubmed_authors><pubmed_authors>Learned K</pubmed_authors><pubmed_authors>Spillinger A</pubmed_authors><pubmed_authors>Currie R</pubmed_authors><pubmed_authors>Lam DL</pubmed_authors><pubmed_authors>Torno L</pubmed_authors><pubmed_authors>Leung SG</pubmed_authors><pubmed_authors>Newton Y</pubmed_authors><pubmed_authors>Liu HY</pubmed_authors><pubmed_authors>Resnick AC</pubmed_authors><pubmed_authors>Laskin J</pubmed_authors><pubmed_authors>Marra MA</pubmed_authors><pubmed_authors>Goldstein TC</pubmed_authors><pubmed_authors>Huynh V</pubmed_authors><pubmed_authors>Deyell RJ</pubmed_authors><pubmed_authors>Rassekh SR</pubmed_authors><pubmed_authors>Swatloski T</pubmed_authors><pubmed_authors>Pfeil J</pubmed_authors><pubmed_authors>Kirov I</pubmed_authors><pubmed_authors>Zabokrtsky KB</pubmed_authors><pubmed_authors>Lacayo N</pubmed_authors><pubmed_authors>Berens ME</pubmed_authors><pubmed_authors>Plant A</pubmed_authors><pubmed_authors>Bjork I</pubmed_authors><pubmed_authors>Haussler D</pubmed_authors><pubmed_authors>Vaske OM</pubmed_authors><pubmed_authors>Sender LS</pubmed_authors><pubmed_authors>Kephart ET</pubmed_authors><pubmed_authors>Sweet-Cordero EA</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Liang WS</pubmed_authors><pubmed_authors>Sanders L</pubmed_authors><pubmed_authors>Lee AG</pubmed_authors><pubmed_authors>Vivian J</pubmed_authors><pubmed_authors>Mueller S</pubmed_authors><pubmed_authors>Salama SR</pubmed_authors><pubmed_authors>Spunt SL</pubmed_authors><pubmed_authors>Rangaswami A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative Tumor RNA Sequencing Analysis for Difficult-to-Treat Pediatric and Young Adult Patients With Cancer.</name><description>&lt;h4>Importance&lt;/h4>Pediatric cancers are epigenetic diseases; therefore, considering tumor gene expression information is necessary for a complete understanding of the tumorigenic processes.&lt;h4>Objective&lt;/h4>To evaluate the feasibility and utility of incorporating comparative gene expression information into the precision medicine framework for difficult-to-treat pediatric and young adult patients with cancer.&lt;h4>Design, setting, and participants&lt;/h4>This cohort study was conducted as a consortium between the University of California, Santa Cruz (UCSC) Treehouse Childhood Cancer Initiative and clinical genomic trials. RNA sequencing (RNA-Seq) data were obtained from the following 4 clinical sites and analyzed at UCSC: British Columbia Children's Hospital (n = 31), Lucile Packard Children's</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2026-04-16T13:10:47.208Z</modification><creation>2020-05-21T18:49:56Z</creation></dates><accession>S-EPMC6822083</accession><cross_references><pubmed>31651965</pubmed><doi>10.1001/jamanetworkopen.2019.13968</doi></cross_references></HashMap>