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scNlaIII-seq

Whole genome sequencing

Identify genetic mutations by profiling hundreds of single cells in parallel and discover the underlying cause of cellular malfunctioning.

  1. Detect SNVs within single cells
  2. Low-cost WGS
  3. Range of coverage for different applications
About scNlaIII-seq
scKaryo-seq

Karyotyping

Identify copy number variations (CNVs) within a chromosome or at the whole chromosome level (aneuploidy) in the genome by profiling hundreds of single cells in parallel and discover the underlying cause of cellular malfunctioning.

  1. Discover CNVs as small as 2 Mbs per cell
  2. Assess the aneuploidy of your sample
  3. Low-cost karyotyping
About scKaryo-seq
scChIC-seq

Chromatin profiling

Look at the specific epigenetic factors influencing DNA-protein binding to regulate gene expression.

  1. Low number of input cells required compared to ChIP-seq
  2. Readily available for key driver histone modifications
  3. Including in-house cell sorting
About scChIC-seq

Single-cell data analysis

Need help with your data analysis, statistics or figure design? Let Single-Cell Core link you to a highly trained bioinformatician.

About Single-cell data analysis
Bulk-seq

Bulk DNA sequencing

Bulk DNA sequencing is the standard tool to generate (epi)genomic data at cell population level.

  1. More powerful and cost-effective compared to scDNA-seq
  2. Low number of 100 input cells required
  3. Can be applied to all our available techiques
About Bulk-seq
1.

Place order

After you have placed your order, we will send the plates to your institute

1 week
2.

Sort single cells

You will sort the cells into the provided plates and send them back to SCC

3.

Processing

Your samples will be processed using our state-of-the-art techniques

4 weeks
4.

Sequencing

The generated libraries will be sequenced

3 weeks
5.

Analysis

The generated data will be analyzed by a bioinformatician upon your request

Contact

06345345

06345345

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