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Theragen Etex Bio

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Suwon, KR

About Theragen Etex Bio

Founded: 1987 Type: Public Company Size: 51-200 employees

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... Show more »

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.

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Our Services (29)


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Whole Exome Sequencing (WES)

Starting at $280.00 per sample

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... Show more »

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

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Illumina HiSeq 2500 Illumina HiSeq 4000 Illumina HiSeq 2000 Human Plants Bacteria Non-human Agilent SureSelect XT Human All Exon v5 Agilent SureSelect XT Human All Exon v4 Show 9 more tags Show less

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RNA Sequencing

Starting at $280.00 per sample

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... Show more »

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

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Illumina HiSeq 2500 Illumina HiSeq 4000 Human Plants Bacteria Non-human Illumina Stranded Total RNA Library Prep Kit Illumina Stranded mRNA Library Prep Kit Illumina TruSeq Small RNA Library Prep Kit Show 9 more tags Show less

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Whole Genome Sequencing

Price on request

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,... Show more »

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.

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Illumina HiSeq X Ten Human Plants Bacteria Non-human

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Truseq RNA Library Preparation

Price on request
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Truseq DNA Library Preparation

Price on request
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Nextera Library Preparation

Price on request
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NGS Data Analysis

Next generation sequencing data analysis
Price on request
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Illumina Sequencing

Price on request
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Targeted Sequencing

Price on request

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.

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.

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Comprehensive Cancer Gene Panel

Price on request

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.

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.

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DNA Sequencing

Price on request
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RNA Services

Price on request
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Biochemistry & Molecular Biology

Price on request
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Nucleic Acid Analysis

Price on request
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Clinical Research

Price on request
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Exome Sequencing Services

Price on request
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Clinical Laboratory Services

Price on request
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Gene Panel Testing

Price on request
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Biology

Price on request
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Nucleic Acid Data Analysis

Price on request
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Targeted Gene Sequencing

Price on request
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Next Generation Sequencing (NGS)

Price on request
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DNA Library Preparation

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DNA Services

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Nucleic Acid Services

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Sequencing Data Analysis and Management

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Clinical Molecular Diagnostics

Price on request
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Illumina NGS Library Preparation

Price on request
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DNA Libraries

Price on request

DNA Libraries Services

DNA Libraries Services

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Claire Kim

NGS sales assistant manager
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Damian So

Marketing Director

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