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SRX20648978: GSM7471637: Trichoplax sp. H2 ATAC; Trichoplax sp. H2; ATAC-seq
4 ILLUMINA (NextSeq 500) runs: 129.1M spots, 10.8G bases, 4.2Gb downloads

External Id: GSM7471637_r1
Submitted by: Sebe-Pedros lab, Systems Biology, Centre for Genomic Regulation
Study: Stepwise emergence of the neuronal gene expression program in early animal evolution
show Abstracthide Abstract
We performed single-cell transcriptome analysis (using 10x) of four placozoan species (Trichoplax adhaerens, Trichoplax sp. H2, Cladtertia collaboinventa, Hoilungia hongkongensis). Additionally we performed bulk ATAC-seq experiments and anti-H3K4me2/anti-H3K4me3 ChIP-seq experiments the same species. Overall design: Adult specimens were fixed, dissociated and pooled before sorting single-cells for scRNAseq. Some samples were mixed (cross-species or cross-treatments) and processed together. Instructions for demultiplexing cells are provided. Please note that the processed data for the scRNA-seq samples are generated from multiple samples (as indicated in the corresponding sample descriptionfield) and thus is linked to the Series records.
Sample: Trichoplax sp. H2 ATAC
SAMN35687519 • SRS17947106 • All experiments • All runs
Library:
Name: GSM7471637
Instrument: NextSeq 500
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: ATAC-seq was performed using the Omni-ATAC protocol (10.1038/nmeth.4396) and using custom Tn5 enzyme Adult specimens were fixed, dissociated and pooled before sorting single-cells for scRNAseq. The same procedure was followed for chromatin profiling experiments, except that cells were used fresh for ATAC-seq and fixed with 1% formaldehyde (10 min) for ChIP-seq
Runs: 4 runs, 129.1M spots, 10.8G bases, 4.2Gb
Run# of Spots# of BasesSizePublished
SRR2488639733,684,9852.8G1.1Gb2023-09-21
SRR2488639828,101,5292.4G946.5Mb2023-09-21
SRR2488639932,576,4542.7G1.1Gb2023-09-21
SRR2488640034,704,2352.9G1.1Gb2023-09-21

ID:
28078215

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