Your Trusted Next-Generation Sequencing Partner

Whole Genome Sequencing

Whole Genome Sequencing is the most comprehensive analysing method as it examines the entire genome of a specimen. Through our extensive sequencing platform options and subsequent data filtering and mapping process, we generate highly accurate, quality data for single nucleotide variants, insertions/deletions, copy number changes, and large structural variants. WGS is available for any specimen types, including human, animal, plant and microorganisms, in both de novo and resequencing approaches.

Transcriptome Sequencing

A transcriptome is a collection of all the transcripts present in a given cell. The sequence of an RNA mirrors the sequence of the DNA from which it was transcribed. Consequently, by analysing the entire collection of RNAs or transcriptome in a cell, researchers can determine when and where each gene is turned on or off in the cells and tissues of an organism.

Whole Exome Sequencing

Exome sequencing would be the most cost-effective approach for sequencing the targeted coding region of a genome, a region that comprises 1–2% of the genome but represents 80–90% of variants found in the entire genome. Therefore, it would be a perfect solution for cancer and genetic-related studies as well as human population studies.

In comparison with WGS (whole genome sequencing), 10–20 times less output is required to analyse SNP (single nucleotide polymorphisms) and Indels, meaning the variant analysis is easier, faster and uses fewer computation resources than the WGS approach.

Metagenome Sequencing

Metagenome sequencing is a method of identifying microbial communities that exist in different environments. It is used primarily to analyse the distribution and types of bacteria and fungi. In other words, it is used to determine which microbial communities are present in a sample collected in a certain environment, and to identify their interactions and roles.