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ZENODO
Dataset . 2021
License: CC BY
Data sources: Datacite
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ZENODO
Dataset . 2021
License: CC BY
Data sources: ZENODO
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2021
License: CC BY
Data sources: Datacite
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Discrete regulatory modules instruct hematopoietic lineage commitment and differentiation

Authors: Georgolopoulos, Grigorios; Psatha, Nikoletta; Iwata, Mineo; Nishida, Andrew; Som, Tannishtha; Yiangou, Minas; Stamatoyannopoulos, John A; +1 Authors

Discrete regulatory modules instruct hematopoietic lineage commitment and differentiation

Abstract

bioRxiv preprint: https://www.biorxiv.org/content/10.1101/2020.04.02.022566v4 Contact: Grigorios Georgolopoulos (ggeorgol@altius.org); Jeff Vierstra (jvierstra@altius.org) Lineage commitment and differentiation is driven by the concerted action of master transcriptional regulators at their target chromatin sites. Multiple efforts have characterized the key transcription factors (TFs) that determine the various hematopoietic lineages. However, the temporal interactions between individual TFs and their chromatin targets during differentiation and how these interactions dictate lineage commitment remains poorly understood. Here we delineate the temporal interplay between the cis- and the trans-regulatory landscape in establishing lineage commitment and differentiation in human hematopoiesis by performing a dense timecourse of chromatin accessibility (DNase I-seq), and gene expression (total and single cell RNA-seq). All data uploaded correspond to human genome build version GRCh38. Contents DNase I Hotspot (DHS) metadata: Supplementary_Data_1.txt DNase I Hotspot quantile-normalized counts: A tab-separated matrix with quantile-normalized DNase I density counts from 79,085 FDR 5% hotspots, across 12 erythroid differentiation timepoints from 3 donors, present in at least n=2 samples. Rows correspond to DHS information in Supplementary_Data_1.txt (hotspots.fdr.0.05.qnorm.counts.tsv.gz) Column information for DNase I Hotspot quantile-normalized counts: hotspots.fdr.0.05.qnorm.counts.info.tsv Developmentally regulated gene metadata (erythroid): Supplementary_Data_2.csv Gene matrix of quantile-normalized FPKM values (erythroid): A tab-separated matrix with the quantile-normalized FPKM values of all detected genes, across 13 erythroid differentiation timepoints from 3 donors. (fpkm_erythroid_qnorm.tsv.gz) Column information for the quantile-normalized FPKM gene matrix (erythroid): A tab-separated table (fpkm_erythroid_qnorm.info.tsv) CD34+ HSPC TADs at 10kb resolution: Supplementary_Data_3.bed Day 11 ex vivo erythroid progenitor TADs at 10kb resolution: Supplementary_Data_4.bed Transcription factor motif enrichment per DHS cluster: Supplementary_Data_5.csv Correlation information (links) between developmentally regulated DHS and target genes: Supplementary_Data_6.csv Chromatin anchor loops called from 10kb resolution Hi-C data: Supplementary_Data_7.bedgraph Developmentally regulated gene metadata (megakaryocytic): Supplementary_Data_8.csv Gene matrix of quantile-normalized FPKM values (megakaryocytic): A tab-separated matrix with the quantile-normalized FPKM values of all detected genes, across 13 megakaryocytic differentiation timepoints from 3 donors. (fpkm_megakaryocyte_qnorm.tsv.gz) Column information for the quantile-normalized FPKM gene matrix (megakaryocytic): A tab-separated table (fpkm_megakaryocyte_qnorm.info.tsv) Marker (differentially expressed) genes per single cell population: Supplementary_Data_9.csv A SCANPY h5ad Annotated DataFrame object: Annotated Data frame `anndata` in h5ad format including the gene-by-cell count matrix, Velocyto splicing kinetics (RNA velocity) information layer, along with obs, obsm, var, varm, and uns layers. (SCANPY_anndata_object.h5ad)

Keywords

chromatin accessibility, gene expression, single cell RNA-seq, differentiation, hematopoiesis, cell identity

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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