Theragen Etex Bio
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Suwon, KR
Theragen Etex Bio Institute is renowned as one of the best genome analysis companies and has a number of accomplishments to prove it. We are the fifth organization in the world that has assembled the entire human genome. In June 2013, we were recognized as the first group to identify genes that are related to Korean gastric cancer. In January 2014, we have secured the cover of the Nature Genetics with our research on the world’s first Minky whale genome.
We offer DNA and RNA sequencing service using state-of-the-art robotics and instrumentation to generate high quality sequence data at affordable prices. We have successfully sequenced countless NGS samples in human, plant and animal from clients all over the world, and our wide range of DNA and RNA sequencing services are highly rated for their turnaround time, quality of results, and competitive prices.
Theragen Etex is fully dedicated to DNA sequencing area, and all of our service portfolios are genomics service strongly based on the most advanced DNA and RNA sequencing technologies including next generation sequencing and bioinformatics. We are now capable of performing various genome projects with research communities including whole Genome, whole Exome sequencing and RNA sequencing with best TAT and high quality data.
Up to 10 samples.
Only for the 1st order.
Sample requirement: 1ug of gDNA
Capture Kit: Agilent SureSelect V5 (50Mb), V6(58Mb)
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.
Exome sequencing is targeting exon regions of the genome. Entire exome is captured using specific kits prior to the sequencing process. Even though sequencing process is essentially the same, it is possible to increase sequencing depth while spending same cost because exome is only a fraction of whole genome.
*This promotion is only for Science Exchange
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.
DNA Libraries Services
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