Single-Cell genomics will help to uncover cell lineage relationships; Single-Cell transcriptomics will supplant the coarse notion of marker-based cell types; and Single-Cell epigenomics and proteomics will allow the functional states of individual cells to be analysed.

• Complete: End-to-end workflow for whole transcriptome analysis of individual cells.
• Highest throughput: Unprecedented parallel processing of up to 96 single cells per run.
• Easiest to use: Less than three hours total hands-on time, working directly from single cells, with no RNA fragmentation and purification step.
  
• Affordable: One-eighth the cost of other library preparation system.

Applications:

•  Profiling scarce clinical samples
•  Measuring intra-tumor heterogeneity and guiding chemotherapy
•  Cancer cells evolution analysis during tumor progression
•   Pre-implantation genetic diagnosis (PGD)

The Single-Cell mRNA solution gives you complete coverage to:

•    Measure expression levels of genes, alleles and spliced variants
•   Compare tissue or cell type expression levels
•    Map transcription initiation sites
•    Characterize alternate splicing patterns
•    Evaluate post-transcriptional activity
•    Discover new transcripts and gene fusions

Whole Genome Amplification for Library Construction for Use with Single Cells and other Applications where DNA is Limited

 CD Genomics's Single-Cell kit produces amplified DNA fragments suitable for Copy Number Variation (CNV) analysis using oligonucleotide aCGH or qPCR; SNP genotyping, mutation detection and sequencing.

CD Genomics’s Single-Cell Sequencing conference focuses on the links between cell variation in tissues and organ function and further elucidates the origins of diseases.