Transcriptomics & Single Cell

SMART-Seq

Use template-switching amplification to investigate full-length transcripts from single cells or low-input RNA.

Principle

SMART-Seq uses reverse-transcriptase template switching to generate and amplify cDNA from single cells or small RNA inputs. Appropriate experiments provide more complete transcript coverage than end-tag strategies.

Applications

  • Profile expression in single cells and low-input RNA samples
  • Identify splice isoforms with suitable transcript coverage
  • Compare transcription during development and differentiation

Method features

  • Supports limited samples and precious cells
  • Full-length coverage assists transcript and splicing analysis
  • Input requirements and detection targets are assessed against sample conditions

Workflow

  1. 01

    Assess single-cell or low-input RNA samples

  2. 02

    Perform template-switching reverse transcription and cDNA amplification

  3. 03

    Prepare, assess and sequence libraries

  4. 04

    Quantify expression and analyze suitable transcript structures

This is a workflow overview. Experimental and analytical details depend on sample conditions and research objectives.

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