EHR vendors have a new standard for sharing disease and phenotype data to aid clinical decision support, particularly in rare and hereditary conditions.
Software being built or updated for COVID-19 in India and Texas should be adaptable to future biosurveillance needs, developers say.
PyxisMap, unveiled at the recent ISMB conference, might soon be able to remove the human element from finding causal variants for rare diseases.
Research presented at the Intelligent Systems for Molecular Biology conference shows promise in uncovering more SNP-phenotype links in GWAS.
Early Efforts to Improve Drug-Induced Liver Injury Detection With Machine Learning Fall Short
Organizers of a data analysis challenge remain hopeful that a recent update to the Connectivity Map resource will lead to breakthroughs in DILI detection by next year.