The technology and biology of single-cell RNA sequencing.
By Aleksandra A. Kolodziejczyk, Jong Kyoung Kim, Valentine Svensson, John C. Marioni, Sarah A. Teichmann. Molecules and Cells, 2015
1,313 citations recorded by the source corpus.
Subfields: Biophysics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/779f1919ab4bac545818971e0e1aad0763db0304
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biophysics
- Nir Yosef
- Sarah A. Teichmann
- Johan L. M. Björkegren
- Li-Ming Gan
- Oscar Franzén
- John C. Marioni
- Christina Kendziorski
- Rhonda L. Bacher
In Molecular Biology
- Fabian J Theis
- John C. Marioni
- Nir Yosef
- Valentine Svensson
- Sarah A. Teichmann
- Aaron T. L. Lun
- Cole Trapnell
- Sandrine Dudoit
Citations in the corpus
- A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications (2017, background): “Approximately 20 different scRNA-seq protocols have been published to date, the fine details of which have been thoroughly discussed elsewhere [56].”
- Revealing the vectors of cellular identity with single-cell genomics (2016, background): “The first is technical variation, which is due to factors such as differences in cell integrity and lysis, RNA capture and cDNA conversion, and detection 38,39 .”
- SCODE: an efficient regulatory network inference algorithm from single-cell RNA-Seq during differentiation (2016, background): “With the advancement of single-cell RNA-Seq (scRNA-Seq), we can now quantify the expression of individual cells and analyze detailed differences among cells [1].”
- Microglia states and nomenclature: A field at its crossroads (2022, neutral): “Another source of complexity comes from evident interspecies differences, 75–77 which can further hamper comparisons.”
- Feature selection and dimension reduction for single-cell RNA-Seq based on a multinomial model (2019, methodology): “Early scRNA-Seq studies using protocols such as SMART-Seq2 [8] analyzed these read counts directly, and several methods were developed to facilitate this [9].”
- An accurate and robust imputation method scImpute for single-cell RNA-seq data (2018, methodology): “Fortunately, single-cell RNA sequencing (scRNA-seq) technologies are now emerging as a powerful tool to capture transcriptome-wide cell-to-cell variability 3 – 5 .”
- Ensemble deep learning in bioinformatics (2020, background): “Gene expression data including microarray, RNA-sequencing (RNA-seq) and, recently, single-cell RNA-seq (scRNA-seq) 63–65 , has been studied extensively to better understand complex diseases and to identify biomarkers that can guide therapeutic decision making.”
- Exponential scaling of single-cell RNA-seq in the past decade (2017, background): “classify and characterise cells at the molecular level (Kolodziejczyk et al., 2015; Trapnell, 2015).”
- A general and flexible method for signal extraction from single-cell RNA-seq data (2017, neutral): “Introduction Single-cell RNA sequencing (scRNA-seq) is a powerful and relatively young technique enabling the characterization of the molecular states of individual cells through their transcriptional profiles [1].”
- PanglaoDB: a web server for exploration of mouse and human single-cell RNA sequencing data (2019, background): “Introduction Single-cell RNA sequencing (scRNA-seq) is a technology that measures gene expression at the single-cell level (1).”
- Transcriptomics technologies (2017, background): “Transcriptomes of different disease states, tissues, or even single cells are now routinely generated [5][6][7].”
- Defining cell types and states with single-cell genomics (2015, background): “For a detailed discussion of these issues, see Stegle et al. (2015); Kolodziejczyk et al. (2015).”