{"paper":{"title":"Connecting the dots across time: Reconstruction of single cell signaling trajectories using time-stamped data","license":"http://arxiv.org/licenses/nonexclusive-distrib/1.0/","headline":"","cross_cats":["cond-mat.stat-mech","cs.CG","cs.CV"],"primary_cat":"q-bio.QM","authors_text":"David Stewart, Jayajit Das, Lewis L. Lanier, Sayak Mukherjee, William Stewart","submitted_at":"2016-09-26T15:56:12Z","abstract_excerpt":"Single cell responses are shaped by the geometry of signaling kinetic trajectories carved in a multidimensional space spanned by signaling protein abundances. It is however challenging to assay large number (>3) of signaling species in live-cell imaging which makes it difficult to probe single cell signaling kinetic trajectories in large dimensions. Flow and mass cytometry techniques can measure a large number (4 - >40) of signaling species but are unable to track single cells. Thus cytometry experiments provide detailed time stamped snapshots of single cell signaling kinetics. Is it possible "},"claims":{"count":0,"items":[],"snapshot_sha256":"258153158e38e3291e3d48162225fcdb2d5a3ed65a07baac614ab91432fd4f57"},"source":{"id":"1609.08035","kind":"arxiv","version":2},"verdict":{"id":null,"model_set":{},"created_at":null,"strongest_claim":"","one_line_summary":"","pipeline_version":null,"weakest_assumption":"","pith_extraction_headline":""},"references":{"count":0,"sample":[],"resolved_work":0,"snapshot_sha256":"258153158e38e3291e3d48162225fcdb2d5a3ed65a07baac614ab91432fd4f57","internal_anchors":0},"formal_canon":{"evidence_count":0,"snapshot_sha256":"258153158e38e3291e3d48162225fcdb2d5a3ed65a07baac614ab91432fd4f57"},"author_claims":{"count":0,"strong_count":0,"snapshot_sha256":"258153158e38e3291e3d48162225fcdb2d5a3ed65a07baac614ab91432fd4f57"},"builder_version":"pith-number-builder-2026-05-17-v1"}