Ontology highlight
ABSTRACT: Background
Protein-DNA binding sites of ChIP-seq experiments are identified where the binding affinity is significant based on a given threshold. The choice of the threshold is a trade-off between conservative region identification and discarding weak, but true binding sites.Results
We rescue weak binding sites using MSPC, which efficiently exploits replicates to lower the threshold required to identify a site while keeping a low false-positive rate, and we compare it to IDR, a widely used post-processing method for identifying highly reproducible peaks across replicates. We observe several master transcription regulators (e.g., SP1 and GATA3) and HDAC2-GATA1 regulatory networks on rescued regions in K562 cell line.Conclusions
We argue the biological relevance of we
SUBMITTER: Jalili V
PROVIDER: S-EPMC10246347 | biostudies-literature | 2023 Jun
REPOSITORIES: biostudies-literature