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Single-cell transcriptomics reveals bimodality in expression and splicing in immune cells
Open accessAbstract
Recent molecular studies have shown that, even when derived from a seemingly homogenous population, individual cells can exhibit substantial differences in gene expression, protein levels and phenotypic output, with important functional consequences. Existing studies of cellular heterogeneity, however, have typically measured only a few pre-selected RNAs or proteins simultaneously, because genomic profiling methods could not be applied to single cells until very recently. Here we use single-cell RNA sequencing to investigate heterogeneity in the response of mouse bone-marrow-derived dendritic cells (BMDCs) to lipopolysaccharide. We find extensive, and previously unobserved, bimodal variation in messenger RNA abundance and splicing patterns, which we validate by RNA-fluorescence in situ hybridization for select transcripts. In particular, hundreds of key immune genes are bimodally expressed across cells, surprisingly even for genes that are very highly expressed at the population average. Moreover, splicing patterns demonstrate previously unobserved levels of heterogeneity between cells. Some of the observed bimodality can be attributed to closely related, yet distinct, known maturity states of BMDCs; other portions reflect differences in the usage of key regulatory circuits. For example, we identify a module of 137 highly variable, yet co-regulated, antiviral response genes. Using cells from knockout mice, we show that variability in this module may be propagated through an interferon feedback circuit, involving the transcriptional regulators Stat2 and Irf7. Our study demonstrates the power and promise of single-cell genomics in uncovering functional diversity between cells and in deciphering cell states and circuits.
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“DCs are mostly post-mitotic, and LPS synchronizes them (27) and causes dramatic regulatory changes from the expression of thousands of transcripts (22, 24, 25) to protein phosphorylation (26).”
From Dynamic profiling of the protein life cycle in response to pathogens (2015) · cites this paper as [27]
In the citing paper
“even cells of the same ‘type’ can exhibit substantial heterogeneity, reflecting finer sub-types, regulated functional variation, or inherent stochasticity1–6”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“Across a set of cells, this manifests as bimodality of gene expression (with one mode at zero). While in some cases such bimodality is due to stochastic (‘bursty’) gene expression40 or more stable variation between cell types and states3, in many others it is dominated by false negatives70,85.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“In analogy to simple observational approaches for inferring gene regulation, correlating the expression profiles of genes or proteins opens the way to elucidating the regulatory mechanisms that control them2,3,41,169,170.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“Leveraging this insight, several studies have analyzed the covariation structure between transcripts or proteins across single cells to infer regulatory relations1–3,41,135,137,168–172.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“Second, because of both stochastic and regulated differences between the cells, each cell forms its own ‘perturbation system’, in which multiple regulators are subtly, or more strongly, perturbed, possibly reducing the need for additional experimental perturbations3,41.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“For example, an analysis (N.Y., A.R. and colleagues3) of the covariation in the expression of ~600 transcripts across 18 dendritic cells detected a module of antiviral gene expression, which included two key transcription factors, STAT2 and IRF7.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“These factors were predicted to control the module because variation in their protein expression levels was expected to propagate downstream and create variation in their targets’ mRNA expression, as well in as their own mRNA expression through autoregulation.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“Similarly, simultaneous analysis of protein and RNA or of epigenomic profiles and RNA can provide mechanistic explanations that relate variations in the state of regulator proteins3 or cis-regulatory loci27,28 to variation in target transcripts.”
From Revealing the vectors of cellular identity with single-cell genomics (2016) · cites this paper as [3]
In the citing paper
“Although single splicing events have been described for ≤200 single cells with statistical confidence 14,15 , full-length mRNA analyses for hundreds of cells have not been reported.”
From Single-cell isoform RNA sequencing characterizes isoforms in thousands of cerebellar cells (2018) · cites this paper as [15]
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Citations
Cites
RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
Li, B., & Dewey, C. N. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-323 · Cited by 22,179
mRNA-Seq whole-transcriptome analysis of a single cell
Tang, F., Barbacioru, C., Wang, Y., Nordman, E., Lee, C., Xu, N., Wang, X., Bodeau, J., Tuch, B. B., Siddiqui, A., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1315 · Cited by 3,969
Cabili, M. N., Trapnell, C., Goff, L. A., Koziol, M. J., Tazón‐Vega, B., Regev, A., & Rinn, J. L. (2011) · Genes & Development · doi:10.1101/gad.17446611 · Cited by 3,551
Self-citationBendall, S. C., Simonds, E. F., Qiu, P., Amir, E.-A. D., Krutzik, P. O., Finck, R., Bruggner, R. V., Melamed, R., Trejo, A., Ornatsky, O. I., et al. (2011) · Science · doi:10.1126/science.1198704 · Cited by 2,279
Causal Protein-Signaling Networks Derived from Multiparameter Single-Cell Data
Sachs, K., Perez, O. D., Pe’er, D., Lauffenburger, D. A., & Nolan, G. P. (2005) · Science · doi:10.1126/science.1105809 · Cited by 1,785
Full-length mRNA-Seq from single-cell levels of RNA and individual circulating tumor cells
Ramsköld, D., Luo, S., Wang, Y.-C., Li, R., Deng, Q., Faridani, O. R., Daniels, G. A., Khrebtukova, I., Loring, J. F., Laurent, L. C., et al. (2012) · Nature Biotechnology · doi:10.1038/nbt.2282 · Cited by 1,609
Analysis and design of RNA sequencing experiments for identifying isoform regulation
Katz, Y., Wang, E. T., Airoldi, E. M., & Burge, C. B. (2010) · Nature Methods · doi:10.1038/nmeth.1528 · Cited by 1,353
CEL-seq: single-cell RNA-seq by multiplexed linear amplification
Hashimshony, T., Wagner, F., Sher, N., & Yanai, I. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.08.003 · Cited by 1,231
Inferring Cellular Networks Using Probabilistic Graphical Models
Friedman, N. (2004) · Science · doi:10.1126/science.1094068 · Cited by 1,211
Counting absolute numbers of molecules using unique molecular identifiers
Kivioja, T., Vähärautio, A., Karlsson, K., Bonke, M., Enge, M., Linnarsson, S., & Taipale, J. (2012) · Nature Methods · doi:10.1038/nmeth.1778 · Cited by 1,010
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Control of Transcript Variability in Single Mammalian Cells
Battich, N., Stoeger, T., & Pelkmans, L. (2015) · Cell · doi:10.1016/j.cell.2015.11.018 · Cited by 324
Cell fate inclination within 2-cell and 4-cell mouse embryos revealed by single-cell RNA sequencingPreprint
Biase, F. H., Cao, X., & Zhong, S. (2014) · Genome Research · doi:10.1101/gr.177725.114 · Cited by 316
The Many Alternative Faces of Macrophage Activation
Hume, D. A. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00370 · Cited by 316
GiniClust: detecting rare cell types from single-cell gene expression data with Gini index
Jiang, L., Chen, H., Pinello, L., & Yuan, G. (2016) · Genome biology · doi:10.1186/s13059-016-1010-4 · Cited by 304
Arisdakessian, C. G., Poirion, O., Yunits, B., Zhu, X., & Garmire, L. X. (2019) · Genome biology · doi:10.1186/s13059-019-1837-6 · Cited by 302
Keren-Shaul, H., Kenigsberg, E., Jaitin, D. A., David, E., Paul, F., Tanay, A., & Amit, I. (2019) · Nature Protocols · doi:10.1038/s41596-019-0164-4 · Cited by 292
Ma, P., Amemiya, H. M., He, L. L., Gandhi, S. J., Nicol, R., Bhattacharyya, R. P., Smillie, C. S., & Hung, D. T. (2023) · Cell · doi:10.1016/j.cell.2023.01.002 · Cited by 291
Resolving host–pathogen interactions by dual RNA-seq
Westermann, A. J., Barquist, L., & Vogel, J. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006033 · Cited by 301
Dura, B., Choi, J.-Y., Zhang, K., Damsky, W., Thakral, D., Bosenberg, M., Craft, J. E., & Fan, R. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1173 · Cited by 285
Single-cell epigenomics: techniques and emerging applications
Schwartzman, O., & Tanay, A. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3980 · Cited by 291
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Sousa, C., Golebiewska, A., Poovathingal, S. K., Kaoma, T., Pires‐Afonso, Y., Martina, S., Coowar, D., Azuaje, F., Skupin, A., Balling, R., et al. (2018) · The EMBO Reports · doi:10.15252/embr.201846171 · Cited by 281
Preparation of Single‐Cell RNA‐Seq Libraries for Next Generation Sequencing
Trombetta, J. J., Gennert, D. G., Lu, D. Y., Satija, R., Shalek, A. K., & Regev, A. (2014) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb0422s107 · Cited by 279
Self-citationDynamic Heterogeneity and DNA Methylation in Embryonic Stem Cells
Singer, Z. S., Yong, J., Tischler, J., Hackett, J. A., Altınok, A., Surani, M. A., Cai, L., & Elowitz, M. B. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.06.029 · Cited by 275
A statistical approach for identifying differential distributions in single-cell RNA-seq experiments
Korthauer, K. D., Chu, L.-F., Newton, M. A., Li, Y., Thomson, J., Stewart, R., & Kendziorski, C. (2016) · Genome Biology · doi:10.1186/s13059-016-1077-y · Cited by 273
Image-based transcriptomics in thousands of single human cells at single-molecule resolution
Battich, N., Stoeger, T., & Pelkmans, L. (2013) · Nature Methods · doi:10.1038/nmeth.2657 · Cited by 269
Regulation of pre-mRNA splicing: roles in physiology and disease, and therapeutic prospects
Rogalska, M. E., Vivori, C., & Valcárcel, J. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00556-8 · Cited by 284
Bifurcation analysis of single-cell gene expression data reveals epigenetic landscape
Marco, E., Karp, R. L., Guo, G., Robson, P., Hart, A. H., Trippa, L., & Yuan, G.-C. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1408993111 · Cited by 268
Ding, S., Chen, X., & Shen, K. (2020) · 癌症:英文版 · doi:10.1002/cac2.12078 · Cited by 275
Transcriptomes of major renal collecting duct cell types in mouse identified by single-cell RNA-seq
Chen, L., Lee, J. W., Chou, C.-L., Nair, A. V., Battistone, M. A., Păunescu, T. G., Merkulova, M., Breton, S., Verlander, J. W., Wall, S. M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1710964114 · Cited by 267
Lu, Y., Xue, Q., Eisele, M. R., Sulistijo, E. S., Brower, K. K., Han, L. G., Amir, E.-A. D., Pe’er, D., Miller‐Jensen, K., & Fan, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416756112 · Cited by 267
Single-Cell Transcriptome Analyses Reveal Signals to Activate Dormant Neural Stem Cells
Luo, Y., Coskun, V., Liang, A., Yu, J., Cheng, L., Ge, W., Shi, Z., Zhang, K., Li, C., Cui, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2015.04.001 · Cited by 264
Extreme heterogeneity of influenza virus infection in single cells
Russell, A. B., Trapnell, C., & Bloom, J. D. (2018) · eLife · doi:10.7554/elife.32303 · Cited by 264
Ecker, J. R., Geschwind, D. H., Kriegstein, A. R., Ngai, J., Osten, P., Polioudakis, D., Regev, A., Šestan, N., Wickersham, I. R., & Zeng, H. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.007 · Cited by 258
Self-citationRichard, A., Loïs, B., Herbach, U., Bonnafoux, A., Morin, V., Vallin, E., Guillemin, A., Gao, N. P., Gunawan, R., Cosette, J., et al. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002585 · Cited by 262
Kim, J. K., Kolodziejczyk, A. A., Ilicic, T., Teichmann, S. A., & Marioni, J. C. (2015) · Nature Communications · doi:10.1038/ncomms9687 · Cited by 251
Alternative mRNA splicing in cancer immunotherapy
Frankiw, L., Baltimore, D., & Li, G. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-019-0195-7 · Cited by 253
Probing cellular heterogeneity in cytokine-secreting immune cells using droplet-based microfluidics
Chokkalingam, V., Tel, J., Wimmers, F., Liu, X., Semenov, S. N., Thiele, J., Figdor, C. G., & Huck, W. T. S. (2013) · Lab on a Chip · doi:10.1039/c3lc50945a · Cited by 247
Single-cell gene expression analysis reveals genetic associations masked in whole-tissue experiments
Wills, Q. F., Livak, K. J., Tipping, A. J., Enver, T., Goldson, A. J., Sexton, D. W., & Holmes, C. C. (2013) · Nature Biotechnology · doi:10.1038/nbt.2642 · Cited by 246
Entering the era of single-cell transcriptomics in biology and medicine
Sandberg, R. (2013) · Nature Methods · doi:10.1038/nmeth.2764 · Cited by 252
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McMahon, A., Rahman, R., Jin, H., Shen, J. L., Fieldsend, A., Luo, W., & Rosbash, M. (2016) · Cell · doi:10.1016/j.cell.2016.03.007 · Cited by 248
Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear
Burns, J. C., Kelly, M. C., Hoa, M., Morell, R. J., & Kelley, M. W. (2015) · Nature Communications · doi:10.1038/ncomms9557 · Cited by 238
Identifying cell populations with scRNASeq
Andrews, T. S., & Hemberg, M. (2017) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2017.07.002 · Cited by 247
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Spitzer, M. H., Gherardini, P. F., Fragiadakis, G. K., Bhattacharya, N., Yuan, R. T., Hotson, A. N., Finck, R., Carmi, Y., Zunder, E. R., Fantl, W. J., et al. (2015) · Science · doi:10.1126/science.1259425 · Cited by 241
Single-cell RNA-sequencing: The future of genome biology is now
Picelli, S. (2016) · RNA Biology · doi:10.1080/15476286.2016.1201618 · Cited by 237
scSLAM-seq reveals core features of transcription dynamics in single cells
Erhard, F., Baptista, M. A. P., Krammer, T., Hennig, T., Lange, M., Arampatzi, P., Jürges, C. S., Theis, F. J., Saliba, A.-E., & Dölken, L. (2019) · Nature · doi:10.1038/s41586-019-1369-y · Cited by 233
High-throughput total RNA sequencing in single cells using VASA-seq
Salmén, F., Jonghe, J. D., Kamiński, T. S., Alemany, A., Parada, G. E., Verity-Legg, J., Yanagida, A., Kohler, T. N., Battich, N., van den Brekel, F., et al. (2022) · Nature Biotechnology · doi:10.1038/s41587-022-01361-8 · Cited by 244
Hawkins, F. J., Krämer, P., Jacob, A., Driver, I. H., Thomas, D. C., McCauley, K. B., Skvir, N. J., Crane, A. M., Kurmann, A. A., Hollenberg, A. N., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci89950 · Cited by 232
Kakaradov, B., Arsenio, J., Widjaja, C. E., He, Z., Aigner, S., Metz, P. J., Yu, B., Wehrens, E. J., Lopez, J. M., Kim, S. H., et al. (2017) · Nature Immunology · doi:10.1038/ni.3688 · Cited by 231
Single-cell transcriptome sequencing: recent advances and remaining challenges
Liu, S., & Trapnell, C. (2016) · F1000Research · doi:10.12688/f1000research.7223.1 · Cited by 230
Pott, S. (2017) · eLife · doi:10.7554/elife.23203 · Cited by 230
Kaletsky, R. L., Yao, V., Williams, A. E., Runnels, A. M., King, S. B., Tadych, A., Zhou, S., Troyanskaya, O. G., & Murphy, C. T. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007559 · Cited by 232
Sarkar, A., & Stephens, M. (2021) · Nature Genetics · doi:10.1038/s41588-021-00873-4 · Cited by 224
Single-Cell Analysis in Cancer Genomics
Saadatpour, A., Lai, S., Guo, G., & Yuan, G. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.07.003 · Cited by 230
Systems biology primer: the basic methods and approaches
Tavassoly, I., Goldfarb, J., & Iyengar, R. (2018) · Essays in Biochemistry · doi:10.1042/ebc20180003 · Cited by 228
A Generic and Cell-Type-Specific Wound Response Precedes Regeneration in Planarians
Wurtzel, O., Cote, L. E., Poirier, A., Satija, R., Regev, A., & Reddien, P. W. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.11.004 · Cited by 221
Self-citationMulti-Scale molecular deconstruction of the serotonin neuron system
Okaty, B. W., Freret, M. E., Rood, B. D., Brust, R. D., Hennessy, M. L., deBairos, D., Kim, J. C., Cook, M. N., & Dymecki, S. M. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.007 · Cited by 217
Every Cell Is Special: Genome-wide Studies Add a New Dimension to Single-Cell Biology
Junker, J. P., & van Oudenaarden, A. (2014) · Cell · doi:10.1016/j.cell.2014.02.010 · Cited by 224
Understanding HIV Latency: The Road to an HIV Cure
Dahabieh, M. S., Battivelli, E., & Verdin, E. M. (2015) · Annual Review of Medicine · doi:10.1146/annurev-med-092112-152941 · Cited by 215
The Dimensions, Dynamics, and Relevance of the Mammalian Noncoding Transcriptome
Deveson, I. W., Hardwick, S. A., Mercer, T. R., & Mattick, J. S. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.04.004 · Cited by 215
Heterogeneity in immune responses: from populations to single cells
Satija, R., & Shalek, A. K. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.03.004 · Cited by 215
Self-citationFields, A. P., Rodriguez, E. H., Jovanović, M., Stern‐Ginossar, N., Haas, B. J., Mertins, P., Raychowdhury, R., Hacohen, N., Carr, S. A., Ingolia, N. T., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.11.013 · Cited by 215
Self-citationTian, L., Jabbari, J. S., Thijssen, R., Gouil, Q. A., Amarasinghe, S. L., Voogd, O., Kariyawasam, H., Du, M. R. M., Schuster, J., Wang, C., et al. (2021) · Genome biology · doi:10.1186/s13059-021-02525-6 · Cited by 215
Computational methods for trajectory inference from single‐cell transcriptomics
Cannoodt, R., Saelens, W., & Saeys, Y. (2016) · European Journal of Immunology · doi:10.1002/eji.201646347 · Cited by 210
Song, Y., Botvinnik, O. B., Lovci, M. T., Kakaradov, B., Liu, P., Xu, J. L., & Yeo, G. W. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.06.003 · Cited by 204
Arsenio, J., Kakaradov, B., Metz, P. J., Kim, S. H., Yeo, G. W.-M., & Chang, J. T. (2014) · Nature Immunology · doi:10.1038/ni.2842 · Cited by 201
Li, F., Huang, Q., Luster, T. A., Hu, H., Zhang, H., Ng, W., Khodadadi‐Jamayran, A., Wang, W., Chen, T., Deng, J., et al. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0780 · Cited by 209
The Emerging Role of Long Noncoding RNAs in Human Disease
DiStefano, J. K. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7471-9_6 · Cited by 203
Butcher, M. J., Filipowicz, A. R., Waseem, T. C., McGary, C. M., Crow, K. J., Magilnick, N., Boldin, M., Lundberg, P. S., & Galkina, E. (2016) · Circulation Research · doi:10.1161/circresaha.116.309764 · Cited by 204
Dynamic control of type I IFN signalling by an integrated network of negative regulators
Porritt, R. A., & Hertzog, P. J. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.02.002 · Cited by 206
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
Oyler‐Yaniv, A., Oyler, J. E., Whitlock, B. M., Liu, Z., Germain, R. N., Huse, M., Altan-Bonnet, G. Y., & Krichevsky, O. (2017) · Immunity · doi:10.1016/j.immuni.2017.03.011 · Cited by 204
Practical considerations for plant phylogenomics
McKain, M. R., Johnson, M. G., Uribe‐Convers, S., Eaton, D. A. R., & Yang, Y. J. (2018) · Applications in Plant Sciences · doi:10.1002/aps3.1038 · Cited by 193
Introduction to Single‐Cell RNA Sequencing
Olsen, T. K., & Baryawno, N. (2018) · Current Protocols in Molecular Biology · doi:10.1002/cpmb.57 · Cited by 201
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Bassler, K. E., Schulte-Schrepping, J., Warnat‐Herresthal, S., Aschenbrenner, A. C., & Schultze, J. L. (2019) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042718-041728 · Cited by 200
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Tang, P. C., Chung, J. Y., Xue, V. W., Xiao, J., Meng, X., Huang, X., Zhou, S., Chan, A. S. W., Tsang, C. M., Cheng, A. S., et al. (2021) · Advanced Science · doi:10.1002/advs.202101235 · Cited by 191
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Wen, L., & Tang, F. (2016) · Genome biology · doi:10.1186/s13059-016-0941-0 · Cited by 195
A Single-Cell Sequencing Guide for Immunologists
See, P., Lum, J., Chen, J., & Ginhoux, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02425 · Cited by 198
Transcriptional mediators of treatment resistance in lethal prostate cancer
He, M. X., Cuoco, M. S., Crowdis, J. P., Bosma-Moody, A., Zhang, Z., Bi, K., Kanodia, A., Su, M.-J., Ku, S., Garcia, M. M., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01244-6 · Cited by 186
Self-citationOlalekan, S. A., Xie, B., Back, R., Eckart, H., & Basu, A. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109165 · Cited by 184
Multiplexed, targeted profiling of single-cell proteomes and transcriptomes in a single reaction
Genshaft, A. S., Li, S., Gallant, C. J., Darmanis, S., Prakadan, S. M., Ziegler, C. G. K., Lundberg, M., Fredriksson, S., Hong, J., Regev, A., et al. (2016) · Genome Biology · doi:10.1186/s13059-016-1045-6 · Cited by 175
Self-citationHigh-Throughput Secretomic Analysis of Single Cells to Assess Functional Cellular Heterogeneity
Lu, Y., Chen, J. J. F., Mu, L., Xue, Q., Wu, Y., Wu, P.-H., Li, J., Vortmeyer, A. O., Miller‐Jensen, K., Wirtz, D., et al. (2013) · Analytical Chemistry · doi:10.1021/ac400082e · Cited by 176
Lee, M.-C. W., López-Díaz, F. J., Khan, S. Y., Tariq, M., Dayn, Y., Vaske, C. J., Radenbaugh, A., Kim, H. J., Emerson, B. M., & Pourmand, N. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404656111 · Cited by 174
Regulation of Neuronal Differentiation, Function, and Plasticity by Alternative Splicing
Furlanis, E., & Scheiffele, P. (2018) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100617-062826 · Cited by 177
Spatiotemporal transcriptomics reveals the evolutionary history of the endoderm germ layer
Hashimshony, T., Feder, M., Levin, M., Hall, B. K., & Yanai, I. (2014) · Nature · doi:10.1038/nature13996 · Cited by 170
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Giladi, A., & Amit, I. (2018) · Cell · doi:10.1016/j.cell.2017.11.011 · Cited by 168
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Landau, D. A., Carter, S. L., Getz, G. A., & Wu, C. J. (2013) · Leukemia · doi:10.1038/leu.2013.248 · Cited by 173
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Metadata
- Authors
- Shalek, A. K., Satija, R., Adiconis, X., Gertner, R. S., Gaublomme, J. T., Raychowdhury, R., Schwartz, S., Yosef, N., Malboeuf, C., Lu, D., Trombetta, J. J., Gennert, D., Gnirke, A., Goren, A., Hacohen, N., Levin, J. Z., Park, H., & Regev, A.
- Affiliations
- Harvard University (US)
- Broad Institute (US)
- Corresponding author
- Park, Hongkun
- Regev, Aviv
- ORCID
- Venue
- Nature
- Published
- 2013-05-19
- Volume
- 498
- Issue
- 7453
- Pages
- 236-240
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3683364
- OpenAlex
- W2110768394
- Cited by
- 1,190
- References
- 30
- Citations by year
- 2026: 29 · 2025: 40 · 2024: 46 · 2023: 65 · 2022: 96 · 2021: 75 · 2020: 104 · 2019: 117 · 2018: 117 · 2017: 120 · 2016: 120 · 2015: 126 · 2014: 92 · 2013: 30
- FWCI
- 54.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion)
- PMC
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (DP1OD003893, 1dp2od002230-01, DP1OD003958)
- National Institute on Drug Abuse (DP1DA035083)
- National Human Genome Research Institute (P50HG006193)
- National Cancer Institute (DP1CA174427)
- National Institute of Allergy and Infectious Diseases (U54AI057159)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (F32HD075541)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Keywords
- bimodal gene expression, single-cell transcriptomics, bone marrow-derived dendritic cells, lipopolysaccharide stimulation, alternative splicing, cellular heterogeneity, interferon pathway, STAT2, IRF7, dendritic cell maturation, cytokine expression, SMART-seq, RNA fluorescence in situ hybridization, gene regulatory circuits
- MeSH terms
- Animals, Bone Marrow Cells, Dendritic Cells, Gene Expression Regulation, Interferons, Lipopolysaccharides, RNA Splicing, RNA, Messenger, Viruses, Reproducibility of Results, In Situ Hybridization, Fluorescence, Sequence Analysis, RNA, Mice, Knockout, Protein Isoforms, Gene Expression Profiling, STAT2 Transcription Factor, Interferon Regulatory Factor-7, Mice, Single-Cell Analysis, Transcriptome
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