Theragen Etex Bio

Up to 10 samples.
Only for the 1st order
Sequencing will be performed on the latest platform.
Illumina HiSeq 2500 with 100X RAW DATA.
TAT: 4 Weeks after QC pass
Data delivery via Theragen's FTP Link
Shipping is Free using our FedEx account number.

RNA analysis using next generation sequencing gave a new era of expression analysis and structural, functional prediction of given genes at a given time.
*This promotion is only for Science Exchange

Whole genome de novo sequencing

Whole genome de novo sequencing requires special library preparation and highly parallel sequencing technology. There are two types of de novo genome sequencing which are draft map and fine map. To construct successful de novo genome, various libraries with different sizes (200bp, 500bp, 2kb, 5kb, 10kb, 20kb) are usually prepared.

Whole genome resequencing

Whole genome re-sequencing is to compare genome sample to available genome reference (Initial sequence of particular genome) for detecting variants (SNPs, Indels). This requires highly parallel system such as Illumina HiSeq to provide sufficient coverage depths for accurate variant detection.

Using customized sequencing service, researchers can select the region of interest within the genome. This approach can utilize ultra deep sequencing of the region of interest for accurate detection of SNVs.

Cancer panel service is for detecting somatic mutations within targeted genes by using combination of deep sequencing (>1000X) and bioinformatics technologies. Because this service utilizes ultra deep sequencing, it is possible to detect somatic mutations in low purity tissue samples such as FFPEs.