The DOI matches its Crossref record; 51 of the 52 references it cites were found in a registry or an index.
Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells
Open accessAbstract
Recent technical developments have enabled the transcriptomes of hundreds of cells to be assayed in an unbiased manner, opening up the possibility that new subpopulations of cells can be found. However, the effects of potential confounding factors, such as the cell cycle, on the heterogeneity of gene expression and therefore on the ability to robustly identify subpopulations remain unclear. We present and validate a computational approach that uses latent variable models to account for such hidden factors. We show that our single-cell latent variable model (scLVM) allows the identification of otherwise undetectable subpopulations of cells that correspond to different stages during the differentiation of naive T cells into T helper 2 cells. Our approach can be used not only to identify cellular subpopulations but also to tease apart different sources of gene expression heterogeneity in single-cell transcriptomes.
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?
The cited source says what the claim attributes to it.
In the citing paper
“Finally, while we focus here on modeling technical variation due to differences in cellular sequencing depth, we note that our approach can be easily extended to model alternative “nuisance” parameters, including cell cycle [31], mitochondrial percentage, or experimental batch, simply by adding additional covariates to the model.”
From Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression (2019) · cites this paper as [31]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“For 709 genes, estimates of fold change in response to IFN-β stimulation in myeloid and CD4+ cells are consistent with estimates in monocyte derived dendritic cells28 and CD4+ T cells27, respectively (Supplementary Fig. 17) and correlated with qPCR results of sorted CD4+ T cells (Supplementary Fig. 18).”
From Multiplexed droplet single-cell RNA-sequencing using natural genetic variation (2018) · cites this paper as [28]
Experimental — accuracy not yet measuredIn the citing paper
“We performed latent variable regression to mitigate heterogeneity resulting from cell-cycle state10,11 (Extended Data Fig. 1), preventing subsequent analysis from being dominated by mitotic phase-specific gene expression”
From Developmental diversification of cortical inhibitory interneurons (2018) · cites this paper as [10]
In the citing paper
“Other biological factors such as cell‐cycle stage can also lead to structure that can mask the signal of interest; computational strategies exist to identify and remove these effects (Buettner et al, 2015).”
From Using single-cell genomics to understand developmental processes and cell fate decisions (2018) · cites this paper as Buettner et al, 2015
In the citing paper
“Other biological factors such as cell‐cycle stage can also lead to structure that can mask the signal of interest; computational strategies exist to identify and remove these effects (Buettner et al, 2015).”
From Using single-cell genomics to understand developmental processes and cell fate decisions (2018) · cites this paper as Buettner et al, 2015
In the citing paper
“Previous work showed that in scRNA-seq analysis, cell cycle genes can overload the major principal components that underlie cell-to-cell variations, thereby masking other, more functionally relevant, differences between cells (Buettner et al., 2015).”
From Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing (2019) · cites this paper as Buettner et al., 2015
In the citing paper
“We propose that coincident expression of counteracting regulatory network components manifests as dynamic instability34.”
From Single-cell analysis of mixed-lineage states leading to a binary cell fate choice (2016) · cites this paper as [34]
In the citing paper
“While removing cell cycle effects can improve the inference of developmental trajectories (Buettner et al, 2015; Vento‐Tormo et al, 2018), cell cycle signals can also be informative of the biology.”
From Current best practices in single-cell RNA-seq analysis: a tutorial (2019) · cites this paper as Buettner et al, 2015
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
Differential expression analysis for sequence count data
Anders, S., & Huber, W. (2010) · Genome Biology · doi:10.1186/gb-2010-11-10-r106 · Cited by 15,581
Trapnell, C., Cacchiarelli, D., Grimsby, J., Pokharel, P., Li, S., Morse, M., Lennon, N. J., Livak, K. J., Mikkelsen, T. S., & Rinn, J. L. (2014) · Nature Biotechnology · doi:10.1038/nbt.2859 · Cited by 7,314
Genome-wide efficient mixed-model analysis for association studies
Zhou, X., & Stephens, M. (2012) · Nature Genetics · doi:10.1038/ng.2310 · Cited by 3,627 · cited 2×
“Owing to efficient implementations of mixed models in applications to GWAS 29,49 , these correlation tests are extremely efficient ( Supplementary Notes ).”
MethodSTRING 8--a global view on proteins and their functional interactions in 630 organisms
Jensen, L. J., Kuhn, M., Stark, M., Chaffron, S., Creevey, C. J., Muller, J., Doerks, T., Julien, P., Roth, A. C., Simonovic, M., et al. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn760 · Cited by 2,498
Posttranscriptional Control of T Cell Effector Function by Aerobic Glycolysis
Chang, C.-H., Curtis, J. D., Maggi, L. B., Faubert, B., Villarino, A. V., O’Sullivan, D., Huang, S. C.-C., van der Windt, G. J. W., Blagih, J., Qiu, J., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.016 · Cited by 2,204
Imaging individual mRNA molecules using multiple singly labeled probes
Raj, A., van den Bogaard, P., Rifkin, S. A., van Oudenaarden, A., & Tyagi, S. (2008) · Nature Methods · doi:10.1038/nmeth.1253 · Cited by 2,028
Quantifying E. coli Proteome and Transcriptome with Single-Molecule Sensitivity in Single Cells
Taniguchi, Y., Choi, P. J., Li, G.-W., Chen, H., Babu, M., Hearn, J., Emili, A., & Xie, X. S. (2010) · Science · doi:10.1126/science.1188308 · Cited by 1,982 · cited 3×
“We show that our single-cell latent variable model (scLVM) allows the identification of otherwise undetectable subpopulations of cells that correspond to different stages during the differentiation of naive T cells into T helper 2 cells.”
BackgroundMethodCapturing Heterogeneity in Gene Expression Studies by Surrogate Variable Analysis
Leek, J. T., & Storey, J. D. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030161 · Cited by 1,930
Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells
Yan, L., Yang, M., Guo, H., Yang, L., Wu, J., Li, R., Liu, P., Lian, Y., Zheng, X., Yan, J., et al. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2660 · Cited by 1,740
The IL-4 receptor: signaling mechanisms and biologic functions
Nelms, K., Keegan, A. D., Zamorano, J., Ryan, J. J., & Paul, W. E. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.701 · Cited by 1,545 · cited 1×
“This set was heavily enriched for genes that have important roles in T H 2 cell differentiation— Il4ra 35 .”
Background
Cited by
Sorted by citations
Items 501–600 of 1,000
Applications of Single-Cell Sequencing for Multiomics
Xu, Y., & Zhou, X. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7717-8_19 · Cited by 22
Ye, Y., Gao, L., & Zhang, S. (2019) · Advanced Science · doi:10.1002/advs.201900986 · Cited by 22
Pinpointing Cell Identity in Time and Space
Savulescu, A. F., Jacobs, C., Negishi, Y., Davignon, L., & Mhlanga, M. M. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00209 · Cited by 23
Norris, D. M., Yang, P., Shin, S., Kearney, A. L., Kim, H. J., Geddes, T. A., Senior, A. M., Fazakerley, D. J., Nguyen, L. K., James, D. E., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102118 · Cited by 19
Exploring dimension-reduced embeddings with SleepwalkPreprint
Ovchinnikova, S., & Anders, S. (2020) · Genome Research · doi:10.1101/gr.251447.119 · Cited by 22
Current and future perspectives of single-cell multi-omics technologies in cardiovascular research
Tan, W. L. W., Seow, W. Q., Zhang, A., Rhee, S., Wong, W. H., Greenleaf, W. J., & Wu, J. C. (2023) · Nature Cardiovascular Research · doi:10.1038/s44161-022-00205-7 · Cited by 22
Fan, D., Cong, Y., Liu, J., Zhang, H., & Du, Z. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113928 · Cited by 21
Single Cell Gene Expression to Understand the Dynamic Architecture of the Heart
Massaia, A., Cháves, P., Samari, S., Miragaia, R. J., Meyer, K. B., Teichmann, S. A., & Noseda, M. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00167 · Cited by 20
Self-citationNuclei on the Rise: When Nuclei-Based Methods Meet Next-Generation Sequencing
Butto, T., Mungikar, K., Baumann, P., Winter, J., Lutz, B., & Gerber, S. (2023) · Cells · doi:10.3390/cells12071051 · Cited by 22
The Poisson distribution model fits UMI-based single-cell RNA-sequencing data
Pan, Y., Landis, J. T., Moorad, R., Wu, D., Marron, J. S., & Dittmer, D. P. (2023) · BMC Bioinformatics · doi:10.1186/s12859-023-05349-2 · Cited by 21
Liu, A., Mair, A., Matos, J. L., Vollbrecht, M., Xu, S., & Bergmann, D. C. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002770 · Cited by 26
Implementation and validation of single-cell genomics experiments in neuroscience
Colonna, M., Konopka, G., Liddelow, S. A., Nowakowski, T. J., Awatramani, R. B., Bateup, H. S., Cadwell, C. R., Caglayan, E., Chen, J. L., Gillis, J., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01814-0 · Cited by 22
Delineating biological and technical variance in single cell expression data
Arzalluz-Luque, Á., Devailly, G., Mantsoki, A., & Joshi, A. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.07.006 · Cited by 21
GM-CSF producing autoreactive CD4+ T cells in type 1 diabetes
Knoop, J., Gavrisan, A., Kuehn, D., Reinhardt, J., Heinrich, M., Hippich, M., Eugster, A., Ockert, C., Ziegler, A., & Bonifacio, E. E. (2017) · Clinical Immunology · doi:10.1016/j.clim.2017.12.002 · Cited by 21
Lei, J. (2020) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2020.110196 · Cited by 23
Single-cell entropy for accurate estimation of differentiation potency from a cell’s transcriptomePreprint
Teschendorff, A. E. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/084202 · Cited by 23
Genetics and immunity in the era of single-cell genomics
Braga, F. A. V., Teichmann, S. A., & Chen, X. X. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw192 · Cited by 20
Self-citationTranscriptional enhancers: from prediction to functional assessment on a genome-wide scale
Tobias, I. C., Abatti, L. E., Moorthy, S. D., Mullany, S., Taylor, T., Khader, N., Filice, M., & Mitchell, J. A. (2020) · Genome · doi:10.1139/gen-2020-0104 · Cited by 25
Singh, S., Sutcliffe, M. D., Repich, K., Atkins, K. A., Harvey, J. A., & Janes, K. A. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-1034 · Cited by 18
Sestrins regulate muscle stem cell metabolic homeostasis
Yang, B. A., Castor‐Macias, J. A., Fraczek, P. M., Cornett, A. M., Brown, L. A., Kim, M., Brooks, S. V., Lombaert, I. M. A., Lee, J. H., & Aguilar, C. A. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.07.014 · Cited by 20
Distinct transcription kinetics of pluripotent cell states
Shao, R., Kumar, B. M., Lidschreiber, K., Lidschreiber, M., Cramer, P., & Elsässer, S. J. (2022) · Molecular Systems Biology · doi:10.15252/msb.202110407 · Cited by 21
Xu, H., Hu, Y., Zhang, X., Aouizerat, B. E., Yan, C., & Xu, K. (2022) · BMC Genomics · doi:10.1186/s12864-021-08235-4 · Cited by 21
scGMAAE: Gaussian mixture adversarial autoencoders for diversification analysis of scRNA-seq data
Wang, H., Zhao, J., Zheng, C.-H., & Su, Y. (2023) · Briefings in Bioinformatics · doi:10.1093/bib/bbac585 · Cited by 20
Fedr, R., Kahounová, Z., Remšík, J., Reiterová, M., Kalina, T., & Souček, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-31990-1 · Cited by 20
Comparison between the Amount of Environmental Change and the Amount of Transcriptome Change
Ogata, N., Kozaki, T., Yokoyama, T., Hata, T., & Iwabuchi, K. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144822 · Cited by 20
Bioinformatics approaches to single-cell analysis in developmental biology
Yalcin, D., Hakguder, Z., & Otu, H. H. (2015) · Molecular Human Reproduction · doi:10.1093/molehr/gav050 · Cited by 20
RNA Exosome and Non-coding RNA-Coupled Mechanisms in AID-Mediated Genomic Alterations
Laffleur, B., Basu, U., & Lim, J. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.12.021 · Cited by 20
McLean, C. K., Narayan, S., Lin, S. Y., Rai, N., Chung, Y., Hipolito, M. S., Cascella, N. G., Nürnberger, J. I., Ishizuka, K., Sawa, A., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0126-6 · Cited by 21
Ranzoni, A. M., Strzelecka, P. M., & Cvejic, A. (2019) · Essays in Biochemistry · doi:10.1042/ebc20180072 · Cited by 21
Hao, J., Cao, W., Huang, J. J., Zou, X., & Han, Z. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty1016 · Cited by 19
Gene regulatory network inference from single-cell data using multivariate information measuresPreprint
Chan, T. E., Stumpf, M. P. H., & Babtie, A. C. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/082099 · Cited by 24
Blasi, T., Buettner, F., Strasser, M. K., Marr, C., & Theis, F. J. (2017) · Physical Biology · doi:10.1088/1478-3975/aa609a · Cited by 18
Self-citationClustering single-cell RNA-seq data by rank constrained similarity learning
Mei, Q., Li, G., & Su, Z. (2021) · Bioinformatics · doi:10.1093/bioinformatics/btab276 · Cited by 22
Zou, J., Deng, F., Wang, M., Zhang, Z., Liu, Z., Zhang, X., Hua, R., Chen, K., Zou, X., & Hao, J. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac180 · Cited by 20
New insights into macrophage subsets in atherosclerosis
Wang, Y., Wang, Q. A., & Xu, D. (2022) · Journal of Molecular Medicine · doi:10.1007/s00109-022-02224-0 · Cited by 19
Decoding brain memory formation by single-cell RNA sequencing
Sardoo, A. M., Zhang, S., Ferraro, T. N., Keck, T. M., & Chen, Y. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac412 · Cited by 20
Kaur, H., Jha, P., Ochatt, S., & Kumar, V. (2023) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2023.2165900 · Cited by 22
Menero‐Valdés, P., Chronakis, M. I., Fernández, B., Quarles, C. D., González‐Iglesias, H., Meermann, B., & Pereiro, R. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.3c02558 · Cited by 19
Singh, A. M. (2015) · Stem Cells International · doi:10.1155/2015/219514 · Cited by 19
Profiling of Single‐Cell Transcriptomes
Chen, W., Gardeux, V., Meireles-Filho, A. C. A., & Deplancke, B. (2017) · Current Protocols in Mouse Biology · doi:10.1002/cpmo.30 · Cited by 16
Transcriptomic Characterization of the Human Cell Cycle in Individual Unsynchronized Cells
Karlsson, J. W., Kroneis, T., Jonasson, E., Larsson, E., & Ståhlberg, A. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.10.011 · Cited by 18
Systems biology: perspectives on multiscale modeling in research on endocrine-related cancers
Clarke, R. C., Tyson, J. J., Tan, M. T., Baumann, W. T., Lu, J., Xuan, J., & Wang, Y. (2019) · Endocrine Related Cancer · doi:10.1530/erc-18-0309 · Cited by 21
Wen, W. X., Mead, A. J., & Thongjuea, S. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.01.009 · Cited by 19
An era of single-cell genomics consortia
Ando, Y., Kwon, A. T.-J., & Shin, J. W. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0409-x · Cited by 20
Chen, Z., Goldwasser, J., Tuckman, P. J., Liu, J. J., Zhang, J., & Gerstein, M. (2022) · Nature Communications · doi:10.1038/s41467-022-31107-8 · Cited by 17
Ma, L., & Zheng, J. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2519-1 · Cited by 20
Reconstructing developmental landscapes and trajectories from single-cell data
Schiebinger, G. R. (2021) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2021.06.002 · Cited by 21
Avesani, S., Viesi, E., Alessandrì, L., Motterle, G., Bonnici, V., Beccuti, M., Calogero, R., & Giugno, R. (2022) · GigaScience · doi:10.1093/gigascience/giac075 · Cited by 17
Incorporating cell hierarchy to decipher the functional diversity of single cells
Chen, L., & Li, S. C. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac1044 · Cited by 18
AGImpute: imputation of scRNA-seq data based on a hybrid GAN with dropouts identification
Zhu, X., Meng, S., Li, G., Wang, J., & Peng, X. (2024) · Bioinformatics · doi:10.1093/bioinformatics/btae068 · Cited by 18
Wang, Z., Jin, S., Liu, G., Zhang, X., Wang, N., Wu, D., Hu, Y., Zhang, C., Jiang, Q., Xu, L., et al. (2017) · BMC Bioinformatics · doi:10.1186/s12859-017-1647-3 · Cited by 17
Cell‐cycle dependence of transcriptome gene modules: comparison of regression lines
Vinogradov, A. E., & Anatskaya, O. V. (2020) · FEBS Journal · doi:10.1111/febs.15257 · Cited by 18
Wang, J., Xia, J., Tan, D., Lin, R., Su, Y., & Zheng, C.-H. (2021) · Briefings in Bioinformatics · doi:10.1093/bib/bbab588 · Cited by 17
G2S3: A gene graph-based imputation method for single-cell RNA sequencing data
Wu, W., Dai, Q., Liu, Y., Yan, X., & Wang, Z. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009029 · Cited by 18
Campbell, K. R., & Yau, C. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/026872 · Cited by 20
Topslam: Waddington Landscape Recovery for Single Cell ExperimentsPreprint
Zwiessele, M., & Lawrence, N. D. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/057778 · Cited by 18
Huang, M. C., Zhang, Z., & Zhang, N. R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.03.234765 · Cited by 14
Dissecting stem cell differentiation using single cell expression profiling
Moignard, V., & Göttgens, B. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.08.005 · Cited by 18
Mind the Map: Technology Shapes the Myeloid Cell Space
Günther, P. S., & Schultze, J. L. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02287 · Cited by 17
Dong, Z., & Alterovitz, G. (2020) · Bioinformatics · doi:10.1093/bioinformatics/btaa669 · Cited by 17
Distinguishing activated T regulatory cell and T conventional cells by single‐cell technologies
Reinhardt, J., Sharma, V., Stavridou, A., Lindner, A., Reinhardt, S., Petzold, A., Lesche, M., Rost, F., Bonifacio, E. E., & Eugster, A. (2022) · Immunology · doi:10.1111/imm.13460 · Cited by 17
Comparison of Database Searching Programs for the Analysis of Single-Cell Proteomics Data
Peng, J., Chan, C. C. H., Meng, F., Hu, Y., Chen, L., Lin, G., Zhang, S., & Wheeler, A. R. (2023) · Journal of Proteome Research · doi:10.1021/acs.jproteome.2c00821 · Cited by 16
Quantifying Cell Heterogeneity and Subpopulations Using Single Cell Metabolomics
Liu, R., Li, J., Lan, Y., Nguyen, T. D., Chen, Y. A., & Yang, Z. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.2c05245 · Cited by 17
SiFT: uncovering hidden biological processes by probabilistic filtering of single-cell data
Piran, Z., & Nitzan, M. (2024) · Nature Communications · doi:10.1038/s41467-024-44757-7 · Cited by 17
Single-cell analysis reveals key roles for Bcl11a in regulating stem cell fate decisions
Powers, A. N., & Satija, R. (2015) · Genome biology · doi:10.1186/s13059-015-0778-y · Cited by 15
Single cell transcriptomics of pluripotent stem cells: reprogramming and differentiation
Natarajan, K. N., Teichmann, S. A., & Kolodziejczyk, A. A. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.06.003 · Cited by 18
Self-citationVicus: Exploiting local structures to improve network-based analysis of biological data
Wang, B., Huang, L., Zhu, Y., Kundaje, A. B., Batzoglou, S., & Goldenberg, A. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005621 · Cited by 17
Kowsar, R., Keshtegar, B., & Miyamoto, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-39081-w · Cited by 17
Sekula, M. N., Gaskins, J., & Datta, S. (2019) · Biometrics · doi:10.1111/biom.13074 · Cited by 18
Shetta, O., & Niranjan, M. (2020) · Royal Society Open Science · doi:10.1098/rsos.190714 · Cited by 17
Single-Cell Transcriptome Analysis Using SINCERA Pipeline
Guo, M., & Xu, Y. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7710-9_15 · Cited by 16
Mercatelli, D., Balboni, N., Palma, A., Aleo, E., Sanna, P. P., Perini, G., & Giorgi, F. M. (2021) · Biomolecules · doi:10.3390/biom11020177 · Cited by 18
zingeR: unlocking RNA-seq tools for zero-inflation and single cell applicationsPreprint
den Berge, K. V., Soneson, C., Love, M. I., Robinson, M. D., & Clement, L. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/157982 · Cited by 17
psupertime: supervised pseudotime inference for single cell RNA-seq data with sequential labelsPreprint
Macnair, W., & Claassen, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/622001 · Cited by 15
Deep Learning Applications in Single-Cell Omics Data AnalysisPreprint
Erfanian, N., Heydari, A. A., Picazo, P. I., Derakhshani, A., GhasemiGol, M., Farahpour, M., Nasseri, S., Safarpour, H., & Sahebkar, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.26.470166 · Cited by 17
Sheinin, R., Sharan, R., & Madi, A. (2025) · Nature Methods · doi:10.1038/s41592-025-02627-0 · Cited by 23
HelPredictor models single-cell transcriptome to predict human embryo lineage allocation
Liang, P., Zheng, L., Long, C., Yang, W., Yang, L., & Zuo, Y. (2021) · Briefings in Bioinformatics · doi:10.1093/bib/bbab196 · Cited by 16
NRF2 is a spatiotemporal metabolic hub essential for the polyfunctionality of Th2 cells
Choi, G., Ju, H.-Y., Bok, J., Choi, J., Shin, J. W., Oh, H., Jeon, Y., Kim, J., Kim, D., Moon, H., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319994121 · Cited by 15
AnomalGRN: deciphering single-cell gene regulation network with graph anomaly detection
Zhou, Z., Wei, J., Liu, M., Zhuo, L., Fu, X., & Zou, Q. (2025) · BMC Biology · doi:10.1186/s12915-025-02177-z · Cited by 16
Ecotoxicity assessment using ciliate cells in millifluidic droplets
Illing, R., Burkart, C., Pfitzner, D., Jungmann, D., Baraban, L., & Cuniberti, G. (2016) · Biomicrofluidics · doi:10.1063/1.4944869 · Cited by 16
De novo prediction of cell-type complexity in single-cell RNA-seq and tumor microenvironments
Woo, J., Winterhoff, B. J. N., Starr, T. K., Aliferis, C., & Wang, J. (2019) · Life Science Alliance · doi:10.26508/lsa.201900443 · Cited by 16
Chawla, S., Samydurai, S., Kong, S. L., Wu, Z., Wang, Z., Tam, W. L., Sengupta, D., & Kumar, V. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkab018 · Cited by 20
Reprogramming progressive cells display low CAG promoter activity
Hu, X., Wu, Q., Zhang, J., Kim, J., Chen, X., Hartman, A. A., Eastman, A. E., Park, I., & Guo, S. (2020) · Stem Cells · doi:10.1002/stem.3295 · Cited by 14
Multi-Omics Profiling of the Tumor Microenvironment
Oekelen, O. V., & Laganà, A. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-91836-1_16 · Cited by 13
Qin, Y., Wu, L. J., Schneider, T., Yen, G. S., Wang, J., Xu, S., Li, M., Paguirigan, A. L., Smith, J. L., Radich, J. P., et al. (2018) · Angewandte Chemie · doi:10.1002/ange.201807314 · Cited by 16
Sun, S., Chen, Y., Liu, Y., & Shang, X. (2019) · BMC Systems Biology · doi:10.1186/s12918-019-0699-6 · Cited by 16
Isoform-level gene expression patterns in single-cell RNA-sequencing data
Vu, T. N., Wills, Q. F., Kalari, K. R., Niu, N., Wang, L., Yudi Pawitan, Y., & Rantalainen, M. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty100 · Cited by 15
Co-expression networks reveal the tissue-specific regulation of transcription and splicingPreprint
Saha, A., Kim, Y., Gewirtz, A. D., Jo, B., Gao, C., McDowell, I. C., Engelhardt, B. E., & Battle, A. J. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/078741 · Cited by 17
HiCat: a semi-supervised approach for cell type annotation
Bi, C., Bai, K., & Zhang, X. (2025) · Briefings in Bioinformatics · doi:10.1093/bib/bbaf428 · Cited by 15
Modeling binary and graded cone cell fate patterning in the mouse retina
Eldred, K. C., Avelis, C. M., Johnston, R. J., & Roberts, E. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007691 · Cited by 15
Lieberman, B., Kusi, M., Hung, C., Chou, C., Ning, H., Ho, Y., Taverna, J. A., Huang, T. H. ‐., & Chen, C. (2020) · Journal of Translational Genetics and Genomics · doi:10.20517/jtgg.2020.51 · Cited by 15
SLRRSC: Single-Cell Type Recognition Method Based on Similarity and Graph Regularization Constraints
Zhang, N.-N., Liu, J., Zheng, C.-H., & Wang, J. (2022) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2022.3148286 · Cited by 16
An update review of the application of single-cell RNA sequencing in pregnancy-related diseases
Zhou, Z., & Yang, X. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1415173 · Cited by 16
Variability in mRNA translation: a random matrix theory approach
Michael Margaliot, A., Huleihel, W., & Tuller, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-84738-0 · Cited by 16
Approximate kNN Classification for Biomedical Data
Anagnostou, P., Barbas, P., Vrahatis, A. G., & Tasoulis, S. K. (2020) · IEEE International Conference on Big Data (BigData) · doi:10.1109/bigdata50022.2020.9378126 · Cited by 15
Single‐cell technologies in reproductive immunology
Vázquez, J., Ong, I. M., & Stanic, A. K. (2019) · American Journal of Reproductive Immunology · doi:10.1111/aji.13157 · Cited by 15
Arrastia, M. V., Jachowicz, J. W., Ollikainen, N., Curtis, M. S., Lai, C., Quinodoz, S. A., Selck, D. A., Guttman, M., & Ismagilov, R. F. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.11.242081 · Cited by 15
Tieng, F. Y. F., Lee, L., & Mutalib, N. A. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10293-z · Cited by 16
Revealing lineage-related signals in single-cell gene expression using random matrix theory
Nitzan, M., & Brenner, M. P. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913931118 · Cited by 15
Metadata
- Authors
- Buettner, F., Natarajan, K. N., Casale, F. P., Proserpio, V., Scialdone, A., Theis, F. J., Teichmann, S. A., Marioni, J. C., & Stegle, O.
- Affiliations
- European Bioinformatics Institute (GB)
- Helmholtz Munich (DE)
- Corresponding author
- Marioni, John C
- Stegle, Oliver
- ORCID
- Venue
- Nature Biotechnology
- Published
- 2015-01-19
- Volume
- 33
- Issue
- 2
- Pages
- 155-160
- ISSN
- 0733-222X (ISSN-L)
- 1087-0156
- 1546-1696
- OpenAlex
- W2010653277
- Cited by
- 1,136
- References
- 52
- Citations by year
- 2026: 27 · 2025: 54 · 2024: 74 · 2023: 79 · 2022: 93 · 2021: 119 · 2020: 133 · 2019: 119 · 2018: 130 · 2017: 144 · 2016: 112 · 2015: 50
- FWCI
- 63.14
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- Site cant be reached (submittedVersion)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion)
- 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 › Molecular Biology › Gene Regulatory Network Analysis
- Keywords
- cellular heterogeneity, single-cell RNA sequencing, cell subpopulations, latent variable models, confounding factors, cell cycle, gene expression heterogeneity, naive T cell differentiation, Th2 cells
- MeSH terms
- Mouse Embryonic Stem Cells, Animals, Cell Differentiation, Models, Theoretical, RNA, Sequence Analysis, RNA, Th2 Cells, Gene Expression Regulation, Developmental, Genetic Heterogeneity, Cell Lineage, Computational Biology, Mice, Single-Cell Analysis, Transcriptome
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