10X Single Cell NANOPORE seq

Single-cell transcriptomics reveals gene expression heterogeneity that is masked in bulk measurements. Long-read, isoform-resolved single-cell sequencing (e.g., nanopore sequencing of single-cell libraries) enables detection of cell-type-specific splicing and transcript isoforms that are difficult to resolve with short-read single-cell RNA-seq. This makes it possible to study processes such as isoform switching during development and differentiation.

For example, Lebrigand et al. showed that the mouse brain gene Clathrin light chain A (Clta) undergoes isoform switching during neuronal maturation, and identified 76 genes with cell-type-specific transcript usage.

Figure adapted from 10X Genomics
Figure adapted from Lebrigand et al. 2020

NXTGNT has ample experience with 10X Genomics library preparation and Oxford nanopore sequencing. With our PromethION P24 system, we can provide the high throughput necessary for single-cell cDNA nanopore sequencing.

Address

NXTGNT
Ghent University,
Faculty of Pharmaceutical Sciences
Ottergemsesteenweg 460
B-9000 Gent
Belgium

Inside the building

When entering the Ghent University Faculty of Pharmaceutical Sciences through the main entrance, elevators will be located in front of you. NXTGNT is situated on the third floor. When exiting the elevators, NXTGNT is located at your right-hand side.

Contact us

nxtgnt@UGent.be

Call: +32 9 264 80 59