Communications BiologyGenomicsPeer-reviewed journal article
TAS-Seq: a robust and sensitive amplification method for bead-based scRNA-seq
Shigeyuki ShichinoiD, Satoshi UehaiD, Shinichi HashimotoiD, Tatsuro OgawaiD, Hiroyasu AokiiD, Bin WuiD, Chang-Yu CheniD, Masahiro Kitabatake, Noriko Ouji-SageshimaiD, Noriyoshi SawabataiD, Takeshi KawaguchiiD, Toshitugu Okayama, Eiji SugiharaiD, Shigeto HontsuiD, Toshihiro ItoiD, Yasunori IwataiD, Takashi Wada, Kazuho IkeoiD, Takaaki SatoiD, Kouji MatsushimaiD
Abstract
Single-cell RNA-sequencing (scRNA-seq) is valuable for analyzing cellular heterogeneity. Cell composition accuracy is critical for analyzing cell-cell interaction networks from scRNA-seq data. We developed terminator-assisted solid-phase cDNA amplification and sequencing (TAS-Seq) for scRNA-seq based on a terminator, terminal transferase, and nanowell/bead-based scRNA-seq platform; TAS-Seq showed high tolerance to variations in the terminal transferase reaction, which complicate the handling of existing terminal transferase-based scRNA-seq methods. In murine and human lung samples, TAS-Seq yielded scRNA-seq data that were highly correlated with flow-cytometric data, showing higher gene-detection sensitivity and more robust detection of important cell-cell interactions and expression of growth factors/interleukins in cell subsets than 10X Chromium v2 and Smart-seq2. Expanding TAS-Seq application will improve understanding and atlas construction of lung biology at the single-cell level.
- organism: mouse
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: cell-cell communication
- research focus: differential expression
- approach: experimental assay
- Citations
- 47
- FWCI
- 3.02
- Field percentile
- top 6%
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