Introduction

HD scRNA-Seq applications

High-Definition single-cell RNA sequencing works best with ultra-low initial inputs (as low as 10 pg RNA). By seeing more genes than classical bulk scRNA-Seq methods, it expands transcriptomic analysis into new scientific applications.

High-definition single-cell differential gene expression analysis

Detailed characterization of cell subpopulations after larger, less sensitive screenings (bulk scRNA-Seq)

Rare cell RNA analysis (e.g., circulating tumor cells (CTCs) or innate lymphoid cells (ILCs))

Subcellular (cytoplasm, organelle) RNA analysis

Single nucleus RNA-Seq

Benefits

LUTHOR HD reaction allows to amplify minuscule amounts of RNA material and to obtain a full understanding of each cell’s gene expression status.

Unmatched sensitivity: See even lowly expressed genes (<10 copies/cell)

UMIs included: Avoid any read count duplicates

Direct RNA amplification: No more gDNA in your reads

Compatible with “less-than-a-cell” inputs: Go below 10 pg

Description

Performance

LUTHOR HD shows outstanding performance with ultra-low input samples – 10 pg – 1 ng (equivalent to 1 – 100 cells).

Up to 95% of genes detected at only 1M read depth

Outstanding sequencing statistics – minimal rRNA and gDNA reads

High reproducibility, even at ultra-low input

Click here to view details on Performance and Workflow of LUTHOR HD.

Lexogen’s LUTHOR HD Application Note has been published in Nature: Advancing High-Definition Single-Cell RNA Sequencing.
Click here to read the full article.