The main reason for using next-generation sequencing is the effective reduction in turnaround time with NGS compared to traditional methods. At the same time, next-generation sequencing makes it possible to analyze the transcriptome and genome of a species in a detailed and holistic way. CD Genomics offers a growing range of services, from library construction to sequencing to complete experimental design and support. Our 10× Chromium-based next-generation sequencing technology can help you advance genome engineering innovation.
Specifications:
1. Process 1-8 samples per run
2. Collect 500-10,000 cells per sample
3. Libraries produced are compatible with all Illumina sequencers
Single Cell Gene Expression
Single Cell Assay for Transposase Accessible Chromatin (ATAC)
Single Cell Multiome (ATAC + Gene Expression)
Customers must provide high viability, accurately counted, single cell suspensions or isolated nuclei. Customer will specify the number of cells per sample to be assayed. Facility staff will use the Chromium to produce Illumina libraries. Libraries can be sequenced on the Illumina NextSeq.
CD Genomics, as a specialist sequencing company, has a large range of sequencers in our NGS Core, including Illumina MiSeq, NovaSeq, PacBio, and more. If you require this service, please contact us directly.
For research use only, not intended for any clinical use.
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