This SuperSeries is composed of the SubSeries listed below.
Overall design: Refer to individual Series
Accession | PRJNA768844; GEO: GSE185380 |
Type | Umbrella project |
Publications | Dichtl S et al., "Gene-selective transcription promotes the inhibition of tissue reparative macrophages by TNF.", Life Sci Alliance, 2022 Apr;5(4) |
Submission | Registration date: 5-Oct-2021 computational Biology, Max-Planck-Institute for biochemistry |
Relevance | Superseries |
Project Data:
Resource Name | Number of Links |
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Sequence data |
SRA Experiments | 1573 |
Publications |
PubMed | 1 |
PMC | 1 |
Other datasets |
BioSample | 1573 |
GEO DataSets | 4 |
Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism encompasses the following 3 sub-projects:
Project Type | Number of Projects |
Epigenomics | 1 |
BioProject accession | Organism | Title |
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PRJNA768838 | Mus musculus | Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism (ATAC-Seq) (computational Biology, Max-Planck-Institute...) |
|
Transcriptome or Gene expression | 2 |
BioProject accession | Organism | Title |
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PRJNA768860 | Mus musculus | Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism (bulk RNA-Seq) (computational Biology, Max-Planck-Institute...) | PRJNA768861 | Mus musculus | Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism (scRNA-Seq) (computational Biology, Max-Planck-Institute...) |
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