Service Description:

Traditional RNA-Seq methods analyzed RNA from an entire population of cells, but only yielded a bulk average of the measurement instead of representing each individual cell's transcriptome. By analyzing the transcriptome of a single cell at a time, the heterogeneity of a sample is captured and resolved to the fundamental unit of living organisms-the cell.

Single cell Seq allows us to analyze the complexity of biological systems, both within a population and over time, at the single-cell level. It has enabled a detailed and unbiased look at the dynamic process in all its forms.

Omics Drive Single-Cell RNA-Seq utilizes the latest technology on the market: the 10x

Genomics瓹hromium� system and Illumina� NovaSeq� 6000. As an early adopter of these platforms, our optimized workflows maximize project flexibility, speed, and data accuracy.

For bulk expression analysis of samples with picograms of RNA or just a few cells, use our Ultra-Low Input RNA-Seq service.

Bioinformatic Analysis:

• Demultiplexes raw base call (BCL) files

• Erforms alignment, filtering, barcode counting, and UMI counting.

• Perform clustering and gene expression analysis.

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 (More upon request)

Pls contact us for more solutions on 10x Genomics瓹hromium� system, we also offer

• Single Cell Transcriptomics
  

• Single Cell Genomics

• Single Cell Eptigenomics