
bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 29, 2024
Abstract Various single-cell modalities covering transcriptomics, epigenetic and spatio-temporal changes in health disease phenotypes are used an exploratory way to understand biological systems at resolution. However, the vast amount of such data is not systematically linked existing biomedical data. Networks have previously been represent harmonized Integrating various resources networks has recently received increasing attention. These aggregated can provide additional insight into biology complex human diseases cell-type level, however, lack inclusion single cell expression Here, we present PICASO framework, which incorporates gene as layer associations between types, phenotypes, drugs genes. The network includes several standardized databases STRING, Uniprot, GeneOntology, Reactome, OmniPath OpenTargets. Using multiple type-specific instances each annotated scored with their respective data, comparisons states be made by computing sub-networks comparing scores conditions. Ultimately, these group-specific will allow identification relevant genes, processes potentially druggable targets, well comparison different measured groups thus communities interactions.
Language: Английский