» Articles » PMID: 24056875

Smart-seq2 for Sensitive Full-length Transcriptome Profiling in Single Cells

Overview
Journal Nat Methods
Date 2013 Sep 24
PMID 24056875
Citations 1227
Authors
Affiliations
Soon will be listed here.
Abstract

Single-cell gene expression analyses hold promise for characterizing cellular heterogeneity, but current methods compromise on either the coverage, the sensitivity or the throughput. Here, we introduce Smart-seq2 with improved reverse transcription, template switching and preamplification to increase both yield and length of cDNA libraries generated from individual cells. Smart-seq2 transcriptome libraries have improved detection, coverage, bias and accuracy compared to Smart-seq libraries and are generated with off-the-shelf reagents at lower cost.

Citing Articles

Crosstalk Signaling Between the Epithelial and Non-Epithelial Compartments of the Mouse Inner Ear.

David A, Biswas S, Soltis M, Eltawil Y, Zhou R, Easow S J Assoc Res Otolaryngol. 2025; .

PMID: 40080263 DOI: 10.1007/s10162-025-00980-7.


Opportunities and challenges in the application of single-cell transcriptomics in plant tissue research.

Luo M, Cao Y, Hong J Physiol Mol Biol Plants. 2025; 31(2):199-209.

PMID: 40070535 PMC: 11890805. DOI: 10.1007/s12298-025-01558-6.


The landscape of cell lineage tracing.

Feng Y, Liu G, Li H, Cheng L Sci China Life Sci. 2025; .

PMID: 40035969 DOI: 10.1007/s11427-024-2751-6.


Systematic reconstruction of molecular pathway signatures using scalable single-cell perturbation screens.

Jiang L, Dalgarno C, Papalexi E, Mascio I, Wessels H, Yun H Nat Cell Biol. 2025; 27(3):505-517.

PMID: 40011560 DOI: 10.1038/s41556-025-01622-z.


Batch correcting single-cell spatial transcriptomics count data with Crescendo improves visualization and detection of spatial gene patterns.

Millard N, Chen J, Palshikar M, Pelka K, Spurrell M, Price C Genome Biol. 2025; 26(1):36.

PMID: 40001084 PMC: 11863647. DOI: 10.1186/s13059-025-03479-9.


References
1.
Plessy C, Bertin N, Takahashi H, Simone R, Salimullah M, Lassmann T . Linking promoters to functional transcripts in small samples with nanoCAGE and CAGEscan. Nat Methods. 2010; 7(7):528-34. PMC: 2906222. DOI: 10.1038/nmeth.1470. View

2.
Carninci P, Hayashizaki Y . High-efficiency full-length cDNA cloning. Methods Enzymol. 1999; 303:19-44. DOI: 10.1016/s0076-6879(99)03004-9. View

3.
Dobin A, Davis C, Schlesinger F, Drenkow J, Zaleski C, Jha S . STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2012; 29(1):15-21. PMC: 3530905. DOI: 10.1093/bioinformatics/bts635. View

4.
Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, Salzberg S . TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 2013; 14(4):R36. PMC: 4053844. DOI: 10.1186/gb-2013-14-4-r36. View

5.
Wang L, Wang S, Li W . RSeQC: quality control of RNA-seq experiments. Bioinformatics. 2012; 28(16):2184-5. DOI: 10.1093/bioinformatics/bts356. View