Genome Sequencing
Whole Genome Sequencing (WGS) provides a deep insight into the DNA sequence of humans, animals, plants, and microbial genomes, with data analysis at the individual or population level. SNP/INDEL/CNV/SV and other variants of the genome can be fully analysed. Our sequencing analysis enables the identification of somatic and germline mutations as well as customized patterns of cancers and other diseases.
Target Capture Sequencing (TCS) allows researchers to extract genomic information from exons or regions of interest in the human or mouse genome with customized probes. TCS technologies, including Whole Exome Sequencing (WES) and Target Region Sequencing (TRS), deliver much higher coverage than whole genome sequencing for the identification of rare variants and can deliver exceptionable prospects for researchers and patients.
Metagenome Sequencing
metagenomic sequencing services provide to efficiently screen for variants and target organisms and describe and compare the diversity of multiple complex environments. Metagenomics solutions, from the study of community structure and species classification to system evolution, gene function, and metabolic network of environmental microorganisms.
Transcriptome Sequencing
Transcriptome Sequencing services offer RNA sequencing for both mRNA and non-coding RNA, including our popular long non-coding RNA sequencing, small RNA sequencing, and circular RNA sequencing services. In order to reveal the interactions between coding and non-coding RNAs in eukaryotes, whole transcriptome sequencing services are also provided. Featured as long reads from the PacBio platform, isoform sequencing enables the read-out to be in the form of full-length mRNA transcripts.
Epigenome Sequencing
Epigenome Sequencing including Whole Genome Bisulfite Sequencing (WGBS) and Reduced-Representation Bisulfite Sequencing (RRBS) for the detection of methylated cytosines on a genome-wide scale with a single nucleotide resolution. This provides insight into the modifying effects of methylation on gene function and expression. With our ChIP-seq and RIP-seq services, protein-DNA interactions (ChIP-seq) and RNA-protein interactions (RIP-seq) can be effectively analyzed.
