Polled Digital Cell Sorter (p-DCS): Automatic identification of hematological cell types from single cell RNA-sequencing clusters
Sergii DomanskyiiD, Anthony SzedlakiD, Nathaniel T. HawkinsiD, Jiayin WangiD, Giovanni PaternostroiD, Carlo PiermarocchiiD
Abstract
BackgroundSingle cell RNA sequencing (scRNA-seq) brings unprecedented opportunities for mapping the heterogeneity of complex cellular environments such as bone marrow, and provides insight into many cellular processes. Single cell RNA-seq, however, has a far larger fraction of missing data reported as zeros (dropouts) than traditional bulk RNA-seq. This makes difficult not only the clustering of cells, but also the assignment of the resulting clusters into predefined cell types based on known molecular signatures, such as the expression of characteristic cell surface markers. ResultsWe present a computational tool for processing single cell RNA-seq data that uses a voting algorithm to identify cells based on approval votes received by known molecular markers. Using a stochastic procedure that accounts for biases due to dropout errors and imbalances in the number of known molecular signatures for different cell types, the method computes the statistical significance of the final approval score and automatically assigns a cell type to clusters without an expert curator. We demonstrate the utility of the tool in the analysis of eight samples of bone marrow from the Human Cell Atlas. The tool provides a systematic identification of cell types in bone marrow based on a recently-published manually-curated cell marker database [1], and incorporates a suite of visualization tools that can be overlaid on a t-SNE representation. The software is freely available as a python package at https://github.com/sdomanskyi/DigitalCellSorter ConclusionsThis methodology assures that extensive marker to cell type matching information is taken into account in a systematic way when assigning cell clusters to cell types. Moreover, the method allows for a high throughput processing of multiple scRNA-seq datasets, since it does not involve an expert curator, and it can be applied recursively to obtain cell sub-types. The software is designed to allow the user to substitute the marker to cell type matching information and apply the methodology to different cellular environments.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 35
- FWCI
- 2.32
- Field percentile
- top 10%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Digital Cell Sorter (DCS): a cell type identification, anomaly detection, and Hopfield landscapes toolkit for single-cell transcriptomics
Sergii Domanskyi, Alex Hakansson, … Carlo Piermarocchi·PeerJPeer-reviewed·Jan 13, 2021
- SCMarker: ab initio marker selection for single cell transcriptome profiling
Fang Wang, Shaoheng Liang, … Ken Chen·PLoS Computational BiologyPeer-reviewed·Oct 28, 2019
- Evaluation of methods to assign cell type labels to cell clusters from single-cell RNA-sequencing data
J. Javier Díaz-Mejía, Elaine C. Meng, … John H. Morris·F1000ResearchPeer-reviewed·Mar 15, 2019
- Detecting cell type from single cell RNA sequencing based on deep bi-stochastic graph regularized matrix factorization
Wei Lan, Jianwei Chen, … Yi‐Ping Phoebe Chen·bioRxiv·May 16, 2022
- Fully-automated and ultra-fast cell-type identification using specific marker combinations from single-cell transcriptomic data
Aleksandr Ianevski, Anil Kumar Giri, Tero A. Aittokallio·Nature CommunicationsPeer-reviewed·Mar 10, 2022
- Clustering single-cell RNA-seq data by rank constrained similarity learning
Qinglin Mei, Guojun Li, Zhengchang Su·BioinformaticsPeer-reviewed·Apr 23, 2021