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ZENODO
Dataset . 2023
License: CC BY
Data sources: Datacite
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 . 2023
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 . 2023
License: CC BY
Data sources: Datacite
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CamaraLab/ConDecon : Tutorial Data

Authors: , Aubin;

CamaraLab/ConDecon : Tutorial Data

Abstract

ConDecon is a clustering-independent deconvolution method for estimating cell abundances in bulk tissues using single-cell RNA-seq data. The aim of ConDecon is to infer a probability distribution across a reference single-cell dataset that represents the likelihood for each cell in the reference data to be present in the query bulk tissue. ConDecon enables previously elusive analyses of dynamic cellular processes in bulk tissues and represents an increase in functionality and phenotypic resolution with respect to current methods for gene expression deconvolution. We anticipate that these features will improve our understanding of tissue cell composition by facilitating the inference of cell state abundances within complex bulk tissues, particularly in the context of evolving systems like development and disease progression. In the ConDecon GitHub repository, we demonstrate ConDecon's utility by applying it to transcriptomic data (ConDecon_B_cell_Tutorial), spatial transcriptomic data (ConDecon_Spatial_RNA_Tutorial), and chromatin accessibility data (ConDecon_ATAC_Tutorial). These datasets were downloaded from open-source data repositories (referenced below) and re-processed by the Camara lab. For convenience, the re-processed data associated with these tutorials has been uploaded below. Aubin, R. G., Montelongo, J., Hu, R., Camara, P. G. Clustering-independent estimation of cell abundances in bulk tissue using single-cell RNA-seq data. Biorxiv (2023).

{"references": ["The Tabula Muris Consortium. A single-cell transcriptomic atlas characterizes ageing tissues in the mouse. Nature 583, 590\u2013595 (2020). https://doi.org/10.1038/s41586-020-2496-1", "Liu, Chang, et al. Spatiotemporal mapping of gene expression landscapes and developmental trajectories during zebrafish embryogenesis. Developmental Cell 57.10 (2022): https://doi.org/10.1016/j.devcel.2022.04.009.", "Bravo Gonz\u00e1lez-Blas, C., Minnoye, L., Papasokrati, D. et al. cisTopic: cis-regulatory topic modeling on single-cell ATAC-seq data. Nat Methods 16, 397\u2013400 (2019). https://doi.org/10.1038/s41592-019-0367-1"]}

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selected citations
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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).
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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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