<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Noren DP</submitter><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NLM NIH HHS</funding><funding>National Institutes of Health</funding><pagination>e1004890</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4924788</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(6)</volume><pubmed_abstract>Acute Myeloid Leukemia (AML) is a fatal hematological cancer. The genetic abnormalities underlying AML are extremely heterogeneous among patients, making prognosis and treatment selection very difficult. While clinical proteomics data has the potential to improve prognosis accuracy, thus far, the quantitative means to do so have yet to be developed. Here we report the results and insights gained from the DREAM 9 Acute Myeloid Prediction Outcome Prediction Challenge (AML-OPC), a crowdsourcing effort designed to promote the development of quantitative methods for AML prognosis prediction. We identify the most accurate and robust models in predicting patient response to therapy, remission duration, and overall survival. We further investigate patient response to therapy, a clinically actionab</pubmed_abstract><journal>PLoS computational biology</journal><pubmed_title>A Crowdsourcing Approach to Developing and Assessing Prediction Algorithms for AML Prognosis.</pubmed_title><pmcid>PMC4924788</pmcid><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>U54 HG007990</funding_grant_id><funding_grant_id>T15LM007093</funding_grant_id><funding_grant_id>T15 LM007093</funding_grant_id><pubmed_authors>Di Camillo B</pubmed_authors><pubmed_authors>DREAM 9 AML-OPC Consortium</pubmed_authors><pubmed_authors>Santhanam N</pubmed_authors><pubmed_authors>Lin X</pubmed_authors><pubmed_authors>Estrada A</pubmed_authors><pubmed_authors>Wright W</pubmed_authors><pubmed_authors>Hess K</pubmed_authors><pubmed_authors>Fitzgerald A</pubmed_authors><pubmed_authors>Krstajic D</pubmed_authors><pubmed_authors>Zuk P</pubmed_authors><pubmed_authors>Anbrosini G</pubmed_authors><pubmed_authors>Yeung KY</pubmed_authors><pubmed_authors>Kumar S</pubmed_authors><pubmed_authors>Hunter GA</pubmed_authors><pubmed_authors>Hunter G</pubmed_authors><pubmed_authors>Hung LH</pubmed_authors><pubmed_authors>Zolfaghar K</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Cheong JH</pubmed_authors><pubmed_authors>Naegle K</pubmed_authors><pubmed_authors>Piraino SW</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Wrzesien M</pubmed_authors><pubmed_authors>Engquist E</pubmed_authors><pubmed_authors>Ou Yang TH</pubmed_authors><pubmed_authors>Baladandayuthapani V</pubmed_authors><pubmed_authors>Anastassiou D</pubmed_authors><pubmed_authors>Rudnicki W</pubmed_authors><pubmed_authors>Flynn J</pubmed_authors><pubmed_authors>Fatemi SA</pubmed_authors><pubmed_authors>Chen GM</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Bucher P</pubmed_authors><pubmed_authors>Creighton CJ</pubmed_authors><pubmed_authors>Schultz A</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Rosciszewski A</pubmed_authors><pubmed_authors>Guha S</pubmed_authors><pubmed_authors>Ronan T</pubmed_authors><pubmed_authors>Fronczuk M</pubmed_authors><pubmed_authors>Bisberg AJ</pubmed_authors><pubmed_authors>Rhrissorrakrai K</pubmed_authors><pubmed_authors>Yang T</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Kim D</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Stepanov O</pubmed_authors><pubmed_authors>Oehler VG</pubmed_authors><pubmed_authors>Long BL</pubmed_authors><pubmed_authors>Kim M</pubmed_authors><pubmed_authors>Norel R</pubmed_authors><pubmed_authors>Kornblau S</pubmed_authors><pubmed_authors>Tang H</pubmed_authors><pubmed_authors>Vilar JM</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Peabody A</pubmed_authors><pubmed_authors>Niemiec R</pubmed_authors><pubmed_authors>Norman T</pubmed_authors><pubmed_authors>McMurray J</pubmed_authors><pubmed_authors>Korra J</pubmed_authors><pubmed_authors>Shay J</pubmed_authors><pubmed_authors>Rrhissorrakrai K</pubmed_authors><pubmed_authors>Sanavia T</pubmed_authors><pubmed_authors>Zang X</pubmed_authors><pubmed_authors>Morgan D</pubmed_authors><pubmed_authors>Gu W</pubmed_authors><pubmed_authors>Kuh A</pubmed_authors><pubmed_authors>Noren DP</pubmed_authors><pubmed_authors>Hu CW</pubmed_authors><pubmed_authors>Qutub AA</pubmed_authors><pubmed_authors>Campion L</pubmed_authors><pubmed_authors>Hosseini M</pubmed_authors><pubmed_authors>Abrams Z</pubmed_authors><pubmed_authors>Hwang TH</pubmed_authors><pubmed_authors>Friend SH</pubmed_authors><pubmed_authors>Pattin A</pubmed_authors><pubmed_authors>Boutros PC</pubmed_authors><pubmed_authors>Buturovic L</pubmed_authors><pubmed_authors>Motiwala T</pubmed_authors><pubmed_authors>Xiao G</pubmed_authors><pubmed_authors>Regan K</pubmed_authors><pubmed_authors>Batten K</pubmed_authors><pubmed_authors>Dreos R</pubmed_authors><pubmed_authors>Stolovitzky G</pubmed_authors><pubmed_authors>Lescarbeau R</pubmed_authors><pubmed_authors>Ye J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Crowdsourcing Approach to Developing and Assessing Prediction Algorithms for AML Prognosis.</name><description>Acute Myeloid Leukemia (AML) is a fatal hematological cancer. The genetic abnormalities underlying AML are extremely heterogeneous among patients, making prognosis and treatment selection very difficult. While clinical proteomics data has the potential to improve prognosis accuracy, thus far, the quantitative means to do so have yet to be developed. Here we report the results and insights gained from the DREAM 9 Acute Myeloid Prediction Outcome Prediction Challenge (AML-OPC), a crowdsourcing effort designed to promote the development of quantitative methods for AML prognosis prediction. We identify the most accurate and robust models in predicting patient response to therapy, remission duration, and overall survival. We further investigate patient response to therapy, a clinically actionab</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jun</publication><modification>2025-06-01T01:39:01.629Z</modification><creation>2025-06-01T01:39:01.629Z</creation></dates><accession>S-EPMC4924788</accession><cross_references><pubmed>27351836</pubmed><doi>10.1371/journal.pcbi.1004890</doi></cross_references></HashMap>