Nature, Journal Year: 2016, Volume and Issue: 539(7628), P. 309 - 313
Published: Nov. 1, 2016
Language: Английский
Nature, Journal Year: 2016, Volume and Issue: 539(7628), P. 309 - 313
Published: Nov. 1, 2016
Language: Английский
Nature Communications, Journal Year: 2017, Volume and Issue: 8(1)
Published: Jan. 16, 2017
Abstract Characterizing the transcriptome of individual cells is fundamental to understanding complex biological systems. We describe a droplet-based system that enables 3′ mRNA counting tens thousands single per sample. Cell encapsulation, up 8 samples at time, takes place in ∼6 min, with ∼50% cell capture efficiency. To demonstrate system’s technical performance, we collected data from ∼250k across 29 samples. validated sensitivity and its ability detect rare populations using lines synthetic RNAs. profiled 68k peripheral blood mononuclear characterize large immune populations. Finally, used sequence variation determine host donor chimerism single-cell resolution bone marrow isolated transplant patients.
Language: Английский
Citations
5905Science, Journal Year: 2016, Volume and Issue: 352(6282), P. 189 - 196
Published: April 7, 2016
To explore the distinct genotypic and phenotypic states of melanoma tumors, we applied single-cell RNA sequencing (RNA-seq) to 4645 single cells isolated from 19 patients, profiling malignant, immune, stromal, endothelial cells. Malignant within same tumor displayed transcriptional heterogeneity associated with cell cycle, spatial context, a drug-resistance program. In particular, all tumors harbored malignant two states, such that characterized by high levels MITF transcription factor also contained low elevated AXL kinase. Single-cell analyses suggested microenvironmental patterns, including cell-to-cell interactions. Analysis tumor-infiltrating T revealed exhaustion programs, their connection activation clonal expansion, variability across patients. Overall, begin unravel cellular ecosystem how genomics offers insights implications for both targeted immune therapies.
Language: Английский
Citations
4272Cell, Journal Year: 2015, Volume and Issue: 162(1), P. 184 - 197
Published: June 18, 2015
Language: Английский
Citations
2147Cell, Journal Year: 2017, Volume and Issue: 171(7), P. 1611 - 1624.e24
Published: Nov. 30, 2017
Language: Английский
Citations
2139Nature, Journal Year: 2015, Volume and Issue: 523(7561), P. 486 - 490
Published: June 17, 2015
Language: Английский
Citations
2079Cellular and Molecular Immunology, Journal Year: 2020, Volume and Issue: 17(8), P. 807 - 821
Published: July 1, 2020
Abstract Immunotherapy has revolutionized cancer treatment and rejuvenated the field of tumor immunology. Several types immunotherapy, including adoptive cell transfer (ACT) immune checkpoint inhibitors (ICIs), have obtained durable clinical responses, but their efficacies vary, only subsets patients can benefit from them. Immune infiltrates in microenvironment (TME) been shown to play a key role development will affect outcomes patients. Comprehensive profiling tumor-infiltrating cells would shed light on mechanisms cancer–immune evasion, thus providing opportunities for novel therapeutic strategies. However, highly heterogeneous dynamic nature TME impedes precise dissection intratumoral cells. With recent advances single-cell technologies such as RNA sequencing (scRNA-seq) mass cytometry, systematic interrogation is feasible provide insights into functional diversities In this review, we outline progress particularly by focusing landmark studies characterization tumor-associated cells, summarize phenotypic connections with immunotherapy. We believe review could strengthen our understanding facilitate elucidation modulation progression, guide immunotherapies treatment.
Language: Английский
Citations
2019Cell, Journal Year: 2019, Volume and Issue: 178(4), P. 835 - 849.e21
Published: July 18, 2019
Language: Английский
Citations
1990Nature Methods, Journal Year: 2018, Volume and Issue: 15(12), P. 1053 - 1058
Published: Nov. 21, 2018
Language: Английский
Citations
1772Nature, Journal Year: 2016, Volume and Issue: 529(7586), P. 298 - 306
Published: Jan. 1, 2016
Language: Английский
Citations
1754Molecular Systems Biology, Journal Year: 2019, Volume and Issue: 15(6)
Published: June 1, 2019
Single-cell RNA-seq has enabled gene expression to be studied at an unprecedented resolution. The promise of this technology is attracting a growing user base for single-cell analysis methods. As more tools are becoming available, it increasingly difficult navigate landscape and produce up-to-date workflow analyse one's data. Here, we detail the steps typical analysis, including pre-processing (quality control, normalization, data correction, feature selection, dimensionality reduction) cell- gene-level downstream analysis. We formulate current best-practice recommendations these based on independent comparison studies. have integrated into workflow, which apply public dataset further illustrate how work in practice. Our documented case study can found https://www.github.com/theislab/single-cell-tutorial This review will serve as tutorial new entrants field, help established users update their pipelines.
Language: Английский
Citations
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