The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
ACTINN: automated identification of cell types in single cell RNA sequencing
Open accessPublished version of a preprint
Abstract
Abstract Cell type identification is one of the major goals in single cell RNA sequencing (scRNA-seq). Current methods for assigning cell types typically involve the use of unsupervised clustering, the identification of signature genes in each cluster, followed by a manual lookup of these genes in the literature and databases to assign cell types. However, there are several limitations associated with these approaches, such as unwanted sources of variation that influence clustering and a lack of canonical markers for certain cell types. Here, we present ACTINN (Automated Cell Type Identification using Neural Networks), which employs a neural network with 3 hidden layers, trains on datasets with predefined cell types, and predicts cell types for other datasets based on the trained parameters. We trained the neural network on a mouse cell type atlas (Tabula Muris Atlas) and a human immune cell dataset, and used it to predict cell types for mouse leukocytes, human PBMCs and human T cell sub types. The results showed that our neural network is fast and accurate, and should therefore be a useful tool to complement existing scRNA-seq pipelines. Author Summary Single cell RNA sequencing (scRNA-seq) provides high resolution profiling of the transcriptomes of individual cells, which inevitably results in high volumes of data that require complex data processing pipelines. Usually, one of the first steps in the analysis of scRNA-seq is to assign individual cells to known cell types. To accomplish this, traditional methods first group the cells into different clusters, then find marker genes, and finally use these to manually assign cell types for each cluster. Thus these methods require prior knowledge of cell type canonical markers, and some level of subjectivity to make the cell type assignments. As a result, the process is often laborious and requires domain specific expertise, which is a barrier for inexperienced users. By contrast, our neural network ACTINN automatically learns the features for each predefined cell type and uses these features to predict cell types for individual cells. This approach is computationally efficient and requires no domain expertise of the tissues being studied. We believe ACTINN allows users to rapidly identify cell types in their datasets, thus rendering the analysis of their scRNA-seq datasets more efficient.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Furthermore, the parameter settings of HVG selection and PCA in these methods are far to reach a consensus and inevitably introduce artificial bias for performance evaluation 15- 19 .”
From scBERT as a Large-scale Pretrained Deep Language Model for Cell Type Annotation of Single-cell RNA-seq Data (2021) · cites this paper as [15]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Integrating single-cell transcriptomic data across different conditions, technologies, and species
Butler, A., Hoffman, P., Smibert, P., Papalexi, E., & Satija, R. (2018) · Nature Biotechnology · doi:10.1038/nbt.4096 · Cited by 13,174
Massively parallel digital transcriptional profiling of single cells
Zheng, G. X. Y., Terry, J. M., Belgrader, P., Ryvkin, P., Bent, Z. W., Wilson, R., Ziraldo, S. B., Wheeler, T. D., McDermott, G. P., Zhu, J., et al. (2017) · Nature Communications · doi:10.1038/ncomms14049 · Cited by 7,353
Deep generative modeling for single-cell transcriptomics
Lopez, R., Regier, J., Cole, M. B., Jordan, M. I., & Yosef, N. (2018) · Nature Methods · doi:10.1038/s41592-018-0229-2 · Cited by 2,530
Batch effects in single-cell RNA-sequencing data are corrected by matching mutual nearest neighbors
Haghverdi, L., Lun, A. T. L., Morgan, M. D., & Marioni, J. C. (2018) · Nature Biotechnology · doi:10.1038/nbt.4091 · Cited by 2,416
Single-cell RNA sequencing technologies and bioinformatics pipelines
Hwang, B., Lee, J. H., & Bang, D. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0071-8 · Cited by 1,866
Winkels, H., Ehinger, E., Vassallo, M., Buscher, K., Dinh, H. Q., Kobiyama, K., Hamers, A. A. J., Cochain, C., Vafadarnejad, E., Saliba, A.-E., et al. (2018) · Circulation Research · doi:10.1161/circresaha.117.312513 · Cited by 547
Tan, Y., & Cahan, P. (2019) · Cell Systems · doi:10.1016/j.cels.2019.06.004 · Cited by 368
Using neural networks for reducing the dimensions of single-cell RNA-Seq data
Lin, C., Jain, S., Kim, H., & Bar-Joseph, Z. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx681 · Cited by 197
Removal of batch effects using distribution-matching residual networks
Shaham, U., Stanton, K., Zhao, J., Li, H., Raddassi, K., Montgomery, R. R., & Kluger, Y. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx196 · Cited by 170
Lieberman, Y., Rokach, L., & Shay, T. (2018) · PLoS ONE · doi:10.1371/journal.pone.0205499 · Cited by 113
Automated identification of Cell Types in Single Cell RNA SequencingPreprint
Ma, F.-Y., & Pellegrini, M. (2019) · bioRxiv · doi:10.1101/532093 · Cited by 75
Self-citationXie, P., Gao, M., Wang, C., Zhang, J., Noel, P., Yang, C., Von Hoff, D., Han, H., Zhang, M. Q., & Lin, W. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz116 · Cited by 74
Generalizable and Scalable Visualization of Single-Cell Data Using Neural Networks
Cho, H., Berger, B., & Peng, J. (2018) · Cell Systems · doi:10.1016/j.cels.2018.05.017 · Cited by 48
Flagged first, then by citations
Research works printed but not linked: 1
- 2010, Proceedings of the thirteenth international conference on artificial intelligence and statistics, PMLR, 9, 249
Cited by
Sorted by citations
Ianevski, A., Giri, A. K., & Aittokallio, T. A. (2022) · Nature Communications · doi:10.1038/s41467-022-28803-w · Cited by 787
A comparison of automatic cell identification methods for single-cell RNA sequencing data
Abdelaal, T., Michielsen, L., Cats, D., Hoogduin, D., Mei, H., Reinders, M. J. T., & Mahfouz, A. (2019) · Genome Biology · doi:10.1186/s13059-019-1795-z · Cited by 628
Large-scale foundation model on single-cell transcriptomics
Hao, M., Gong, J., Zeng, X., Liu, C., Guo, Y., Cheng, X., Wang, T., Ma, J., Zhang, X., & Song, L. (2024) · Nature Methods · doi:10.1038/s41592-024-02305-7 · Cited by 628
Yang, F., Wang, W., Wang, F., Fang, Y., Tang, D., Huang, J., Lu, H., & Yao, J. (2021) · doi:10.1101/2021.12.05.471261 · Cited by 617
Mapping microglia states in the human brain through the integration of high-dimensional techniques
Sankowski, R., Böttcher, C., Masuda, T., Geirsdottir, L., Sagar, Sindram, E., Seredenina, T., Muhs, A., Scheiwe, C., Shah, M. J., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0532-y · Cited by 449
Metadata
- Authors
- Ma, F., & Pellegrini, M.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Pellegrini, Matteo
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-07-29
- Volume
- 36
- Issue
- 2
- Pages
- 533-538
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- OpenAlex
- W2964643116
- Cited by
- 252
- References
- 12
- Citations by year
- 2026: 25 · 2025: 46 · 2024: 45 · 2023: 40 · 2022: 36 · 2021: 35 · 2020: 20 · 2019: 5
- FWCI
- 7.94
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Bioinformatics (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- U.S. Department of Energy Office of Science
- Office of Biological and Environmental Research (DE-FC02-02ER63421)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Cell Image Analysis Techniques
- Keywords
- cell type annotation, single-cell RNA sequencing, neural network classification, human peripheral blood mononuclear cells, T cell subsets, immune cell classification, cell type atlas
- MeSH terms
- Algorithms, Animals, Humans, Cluster Analysis, Sequence Analysis, RNA, Gene Expression Profiling, Mice, Single-Cell Analysis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review