Single Cell Genomics Platform

Single Cell Genome Sequencing Platform

Single cell genome sequencing aims to deepen our understanding of complex microbial systems and diseases in multicellular organisms by isolating contributions of different cellular populations. Meanwhile, the sequencing technology provides a novel perspective for genetics by bringing the study of genomes to the cell level. Many tools have been used to open up new frontiers by dissecting functions of single cells to the biology of organisms and ecosystems. We're committed to developing the latest technologies to uncover genetic secrets within the cells, including but not limited to:

• Pure PCR-based Amplification (low coverage of genome, but better uniformity) - Degenerate oligonucleotide primed PCR (DOP-PCR)
• Isothermal Amplification (covering most of the genome) - Multiple displacement amplification (MDA)
• Hybrid Methods (intermediate coverage and uniformity) - Multiple annealing and looping based amplification cycles (MALBAC)

Single Cell Exome Sequencing Platform

Exome sequencing in the cell is targeted DNA sequencing where exonic regions are captured and then sequenced. Compared to whole-genome sequencing (WGS), exome sequencing is a much more cost-effective approach to study variations in coding regions since the size of the human exome is only ∼1% of the genome. There are different methods to capture the exonic regions for single cell sequencing, including array hybridization and in-solution hybridization.

With the advent of next next-generation sequencing (NGS), today it is feasible to sequence a large number of DNA. Based on NGS development, we have launched a cutting-edge platform for various exome sequencing services, which with our bioinformatics pipeline, can be a powerful tool to study humans' exome, especially cancer patients. Our standard workflow of single-cell exome sequencing consists of project design, exome enrichment (library preparation), sequencing, and data analysis.

Single Cell Targeted Sequencing Platform

Single cell targeted region sequencing is an effective approach to investigate your selected regions of interest by NGS. By using targeted region sequencing panels, single-nucleotide polymorphisms (SNPs), copy number variations (CNVs), insertions/deletions (InDels), and structural variants (SVs) might be discovered rapidly and precisely. Compared with WGS, targeted region sequencing enables accurate detection of rare variants with higher specificity and sensitivity. This method is very cost-effective when handling quantities of samples, which largely reduces the cost per sample.

Notably, we offer fast and accurate targeted region sequencing and bioinformatics analysis that have been thought of an efficient way to diagnose different genetic disorders. The main process of our targeted region sequencing services includes primers/probes designing & synthesis, target regions capture, library construction, paired-end sequencing, and analysis on target sequences. We harbor a lot of experienced scientists who can execute quality management, following every procedure to ensure reliable results.

Single Cell Genotyping Platform

Single cell genotyping is the process of determining differences in the genotype of a sample by examining the DNA sequence using biological tests and comparing it with another DNA sequence or a reference sequence. The genomic DNA samples are often obtained from two contrasting groups of cell groups, with the purpose of identifying differences in the genetic make-up (genotype) which may explain the difference in the phenotype.

Here, we have developed two popular approaches to explore genotyping within cells, which contain sequencing-based single cell genotyping and mass spectrum (MS)-based single cell genotyping. With the help of us, single cell genotyping studies can be designed and applied by clients to identify DNA sequence differences at three distinct levels: