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"Mapping information-rich genotype-phenotype landscapes with genome-scale Perturb-seq" Replogle et al. 2022 processed Perturb-seq datasets
This dataset includes data from three Perturb-seq experiments described in Replogle et al. 2022 (https://doi.org/10.1016/j.cell.2022.05.013):
- K562 genome-scale perturb-seq sampled at day 8 post-transduction (K562_gwps)
- K562 essential-scale perturb-seq sampled at day 6 post-transduction (K562_essential)
- RPE1 essential-scale perturb-seq sampled at day 7 post-transduction (rpe1)
For each dataset, there are four processed Perturb-seq files in AnnData format (https://anndata.readthedocs.io/en/latest/).
- Raw, single-cell expression data for genes expressed at >0.01 UMI per cell (named $pop_raw_singlecell_01.h5ad)
- Raw, pseudo-bulk expression data for genes expressed at >0.01 UMI per cell (named $pop_raw_bulk_01.h5ad)
- gemgroup Z-normalized single-cell expression data for genes expressed at >0.01 UMI per cell (named $pop_normalized_singlecell_01.h5ad)
- gemgroup Z-normalized pseudo-bulk expression data for genes expressed at >0.01 UMI per cell (named $pop_normalized_bulk_01.h5ad)
In the anndata format, the .var annotation details genes while the .obs annotation details single-cells/pseudobulk populations.
Funding
DARPA HR0011-19-2-0007
Center for Genomic Editing and Recording: Development and Application of Next-Generation Genome and Epigenome Editing Methods to Advance the Study and Treatment of Human Disease
National Human Genome Research Institute
Find out more...The role of TMA7 in mitochondrial dysfunction
National Institute of Neurological Disorders and Stroke
Find out more...Predictive engineering of cellular transcriptional state
National Institute of General Medical Sciences
Find out more...History
Research Institution(s)
University of California, San Francisco; Whitehead InstituteContact email
joseph@wi.mit.eduAssociated Preprint DOI
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