bio.autoxiv
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Abstract: Biomedical omics resources are often treated as separate datasets, which fragments insight and limits discovery of shared mechanisms. By crossing geneset libraries from Common Fund programs we can reveal robust molecu…
Abstract: Biomedical omics resources are often treated as separate collections, which limits insight into shared biological mechanisms. To overcome this fragmentation, we crossed gene sets from three NIH Common Fund programs: t…
Abstract: Biomedical omics resources are often treated as isolated collections, which fragments insight and limits the discovery of shared mechanisms across physiological contexts. To overcome this limitation we leveraged the C…
Abstract: Biomedical omics resources are often treated as separate datasets, which fragments insight and limits discovery of shared mechanisms. Crossing datasets from Common Fund programs can reveal robust molecular signatures …