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DNA Link, Inc

Seoul, KR

DNA Link, Inc., established in March, 2000, is a genomic service providing company based in Korea, focusing on research and development in the field of bio-industry and genomic analysis industry. DNA Link, Inc. has constructed a converged analysis system through more than 10 years of experiment and know-how and striving to provide total genomic solution to customers

With the goal of becoming a “Frontier Company in Personalized Medicine”, DNA Link, Inc. produces high-quality data by analysis of genomic information on all species through up-to-date technologies, constructs DB on genomic information to investigate genomic traits in groups through data analysis and interpretation, discovers genomic biomarkers through converged genomic analysis, and strives to lead personalized medicine and new drug development by converging bio technology and information & communications technology to supports total analysis of... Show more »

DNA Link, Inc., established in March, 2000, is a genomic service providing company based in Korea, focusing on research and development in the field of bio-industry and genomic analysis industry. DNA Link, Inc. has constructed a converged analysis system through more than 10 years of experiment and know-how and striving to provide total genomic solution to customers

With the goal of becoming a “Frontier Company in Personalized Medicine”, DNA Link, Inc. produces high-quality data by analysis of genomic information on all species through up-to-date technologies, constructs DB on genomic information to investigate genomic traits in groups through data analysis and interpretation, discovers genomic biomarkers through converged genomic analysis, and strives to lead personalized medicine and new drug development by converging bio technology and information & communications technology to supports total analysis of genomic and clinical information. DNA Link, Inc.’s ultimate goal is to improve the health and quality of life of all mankind globally.

DNA Link is currently in collaboration with Korea’s most renowned clinical research specialists studying genetic effects of various diseases including diabetes, cardiovascular disease, cancer, atopy, and digestive diseases.

In addition to identifying disease-related genes, DNA Link is working to develop disease diagnostic systems as well as personalized treatment methods. Using DNA Chip and Next Generation Sequencing technologies, we are currently developing cancer diagnostic systems by identifying common variants in DNA copy numbers for various cancers including lung cancer and breast cancer.

DNA Link, Inc. will continue to research, develop and challenge in order to make disease prevention and early diagnosis possible, and provide the foundation for personalized medicine which enables the application of customized method of prevention depending on genetic differences person by person. DNA Link, Inc. will contribute to increase the rate of full recovery and expansion of lifespan for the people.

Recent Publications

  • Choi S, Kim HR, Sung CO, Kim J, Kim S, Ahn SM, Choi CM, Chun SM, Choi EK, Kim SW, Kim YH, Lee JY, Song JS, Kim D, Haq F, Lee SY, Lee JE, Jung WR, Jang HY, Yang E, Lee C, Yu E, Kong G, Baek D, Jang SJ. Genomic Alterations in the RB Pathway Indicate Prognostic Outcomes of Early-Stage Lung Adenocarcinoma. Clin Cancer Res. 2014 Oct 7. pii: clincanres.0519.2014. [Epub ahead of print]
  • Ahn SM, Jang SJ, Shim JH, Kim D, Hong SM, Sung CO, Baek D, Haq F, Ansari AA, Lee SY, Chun SM, Choi S, Choi HJ, Kim J, Kim S, Hwang S, Lee YJ, Lee JE, Jung WR, Jang HY, Yang E, Sung WK, Lee NP, Mao M, Lee C, Zucman-Rossi J, Yu E, Lee HC, Kong G. A genomic portrait of resectable hepatocellular carcinomas: Implications of RB1 and FGF19 aberrations for patient stratification. Hepatology. 2014 May 3. doi: 10.1002/hep.27198. [Epub ahead of print]
  • Hae Yong Yoo, Min Kyung Sung, Seung Ho Lee, Sangok Kim, Haeseung Lee, Seongjin Park, Sang Cheol Kim, Byungwook Lee, Kyoohyoung Rho, Jong-Eun Lee, Kwang-Hwi Cho, Wankyu Kim, Hyunjung Ju, Jaesang Kim, Seok Jin Kim, Won Seog Kim, Sanghyuk Lee & Young Hyeh Ko. A recurrent inactivating mutation in RHOA GTPase in angioimmunoblastic T cell lymphoma. Nat. Genet., Published online 02 March 2014 | doi:10.1038/ng.2916
  • Choi H, Jung C, Sohn SK, Kim S, Kim HJ, Kim YK, Kim T, Zhang Z, Shin ES, Lee JE, Moon JH, Kim SH, Kim KH, Mun YC, Kim H, Park J, Kim J, Kim D. Genome-wide genotype-based risk model for survival in acute myeloid leukaemia patients with normal karyotype. Br J Haematol. 2013 Oct;163(1):62-71. doi: 10.1111/bjh.12492.
  • Jung SW, Park NH, Shin JW, Park BR, Kim CJ, Lee JE, Shin ES, Kim JA, Chung YH. Prognostic impact of telomere maintenance gene polymorphisms in hepatocellular carcinoma patients with chronic Hepatitis B. Hepatology. 2013 Aug 1. doi: 10.1002/hep.26655. [Epub ahead of print]
  • Namkung JH, Lee JE, Kim E, Huh IS, Park T, Shin ES, Cho EY, Yang JM. Single nucleotide polymorphism in the FLT4 gene is associated with atopic dermatitis in Koreans. Cytokine. 2013 Apr;62(1):110-4. doi: 10.1016/j.cyto.2013.02.006. Epub 2013 Mar 13.
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DNA Link, Inc has not listed any services.

Biomarker Discovery
Price on request
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Gene expression profiling
TaqMan Assays
TaqMan Gene Expression Assays
Price on request

With the ABI PRISM 7900HT real-time PCR system, we employ an optimized process for genotyping known SNP positions in large sample sets within a very short amount of time.

Features

  • Optimized process for large sample set
  • Low sample input
  • Sample requirement : 10ng/genotype
  • Turnaround time : 5~6... Show more »

With the ABI PRISM 7900HT real-time PCR system, we employ an optimized process for genotyping known SNP positions in large sample sets within a very short amount of time.

Features

  • Optimized process for large sample set
  • Low sample input
  • Sample requirement : 10ng/genotype
  • Turnaround time : 5~6 weeks

Result

Individual genotype raw data, TaqMan probe type,assay ID, allele frequency

ABI PRISM 7900HT real-time PCR system
Assay Mechanism for Allelic Discrimination
Reasonable for large sample set
Low sample input
Sample requirement -10ng/genotype

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Fluidigm Biomark
Price on request

Similar to TaqMan, Biomark is high-throughput multiplex genotyping platform. Biomark’s default formats of 48 samples x 48 assays, 96 samples x 96 assays and 192 samples x 24 assays can be modified to suit the needs of a higher sample set.

Feature

  • Multiplexed genotyping using Taqman® assay (48x48, 96x96, 192x24... Show more »

Similar to TaqMan, Biomark is high-throughput multiplex genotyping platform. Biomark’s default formats of 48 samples x 48 assays, 96 samples x 96 assays and 192 samples x 24 assays can be modified to suit the needs of a higher sample set.

Feature

  • Multiplexed genotyping using Taqman® assay (48x48, 96x96, 192x24 Standard format)
  • proven assay, high throughput
  • flexibility of analysis format
  • Turnaround time : 5~6weeks

Result

Individual genotype raw data, TaqMan probe type, assay ID, allele frequency

Taqman Assay platform
Multiplexing genotyping
192.24 genotyping(192samples x 24assays)
48.48 genotyping (48 samples x 48 assays)
96.96 genotyping (96 samples x 96 assays)
proven assay, high throughput
flexibility of analysis format

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SNP Genotyping
Single Nucleotide Polymorphism Genotyping
Price on request

Through direct sequencing of specific genes of interest using an automated DNA sequencer, our analysis services include SNP Discovery and detecting known SNPs and their frequencies. The genotyping accuracy through sequencing is so high that it is considered by many to be the gold standard for DNA analysis.

Platform | ABI 3730xl... Show more »

Through direct sequencing of specific genes of interest using an automated DNA sequencer, our analysis services include SNP Discovery and detecting known SNPs and their frequencies. The genotyping accuracy through sequencing is so high that it is considered by many to be the gold standard for DNA analysis.

Platform ABI 3730xl DNA Analyzer
Assay Sequencing
Feature From target gene design to data analysis; Novel SNP discovery, LD analysis, TagSNP selection ; Turnaround time : 6 weeks
Result Individual genotype raw data, LD , Haplotype analysis data
  • PCR : Amplification
  • PCR purification : Remove dNTPs and primers
  • Sequencing reaction : ddNTP & dNTP
  • DYE removal
  • RUN ( 3730xl )
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Gene Copy Number Analysis
Price on request

Comparative genomic hybridization(CGH) is used to study CNV(copy-number variations) in genomes.

Example for workflow & requirement

Affymetrix CytoScanHD array

Benefit

CytoScanHD array from Affymetrix can be used to analyze the smallest structural changes through 700,000 SNP markers and more than 2.6M markers... Show more »

Comparative genomic hybridization(CGH) is used to study CNV(copy-number variations) in genomes.

Example for workflow & requirement

Affymetrix CytoScanHD array

Benefit

CytoScanHD array from Affymetrix can be used to analyze the smallest structural changes through 700,000 SNP markers and more than 2.6M markers with copy numbers. It is also useful for discovery of LOH (loss of heterozygosity) associated with UPD (uniparental disomy) and IBD (identical-by-cescent).

Sample requirement

  • DNA Amount: 250ng
  • DNA Qualification: 260/280 1.8~2.0, 260/230 ratio of over 1.5, (by gel image) no RNA, no degradation

Turnaround time

DNA QC: 2~3 days

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Array CGH
Microarray-Based Comparative Genomic Hybridization
Price on request

The Agilent Human Genome CGH Microarray is a dual color array containing 60-mer oligonucleotide probes synthesized in situ using Agilent’s inkjet SurePrint technology. Its comprehensive probe coverage allows genome-wide DNA copy number variation profiling while focusing on known genes, promoters, miRNAs, pseudoautosomal and... Show more »

The Agilent Human Genome CGH Microarray is a dual color array containing 60-mer oligonucleotide probes synthesized in situ using Agilent’s inkjet SurePrint technology. Its comprehensive probe coverage allows genome-wide DNA copy number variation profiling while focusing on known genes, promoters, miRNAs, pseudoautosomal and telomeric regions.

  • Multiple microarray formats and bundled options available
  • Distinct microarray catalog kits containing regions recommended by ISCA
  • Probes annotated against NCBI Build 37 (UCSC hg19, February 2009)

Comparative genomic hybridization (CGH) is used for genomic copy-number variations (CNV) research. CGH microarray technology platform by Agilent, Inc. allows for the discovery of novel oncogene, anti-oncogene, drug target, and biomarkers through identifying chromosomal abnormalities in cancer and genetic disorders.

Types of Agilent Arrays

Many variations of array exist based on the resolution. Not only human, but also arrays for mouse, rat, and chicken are available, and others besides them are also customizable. If you provide us with DNA of high quality, you are guaranteed to receive the finest result possible, and please note that different DNA amount may be required based on the type of chips

Bioinformatics Service

  • Basic analysis
    • CNV analysis software: Agilent Genomic Workbench
    • Algorithm: ADM-1, ADM-2, CBS
    • Aberration summary report ( PDF format file )
    • Aberration report ( EXCEL format file )
  • Advanced analysis
    • Upon request, an advanced analysis is processed through a professional consultation with an extra fee charged.
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Agilent CGH Microarray
DNA/RNA Analysis and Quality Control
Price on request

DNA Link, Inc., the only service provider which is officially authorized by both Affymetrix and Agilent as a Certified Service Provider (CSP) in Korea, offers a wide range of SNP and expression profiling service. DNA Link guarantees the highest quality service through systematic quality control according to CSP standards since... Show more »

DNA Link, Inc., the only service provider which is officially authorized by both Affymetrix and Agilent as a Certified Service Provider (CSP) in Korea, offers a wide range of SNP and expression profiling service. DNA Link guarantees the highest quality service through systematic quality control according to CSP standards since 2006. Moreover, DNA Link’s research team is very experienced with knowhow from performing many national projects and services, including analysis of more than 50,000 arrays.

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Small RNA Sequencing
Price on request

Small RNA Sequencing analyzes only Small RNA using NGS platform.

Query thousands of small RNA sequences with unprecedented sensitivity and dynamic range for both small RNA discovery and profiling applications. Find novel microRNAs, characterize variation such as isomiRs with single-base resolution, and analyze the differential... Show more »

Small RNA Sequencing analyzes only Small RNA using NGS platform.

Query thousands of small RNA sequences with unprecedented sensitivity and dynamic range for both small RNA discovery and profiling applications. Find novel microRNAs, characterize variation such as isomiRs with single-base resolution, and analyze the differential expression of all small RNAs in any sample without prior assumptions.

Benefit

  • Due to the wide dynamic range of detection, it works for all small RNA.
  • Not just known miRNA, but it can detect novel miRNA and make a prediction.
  • Universal Platform
  • Customizable Size Selection
  • Simple Workflow

Sample requirements

Hiseq Proton/PGM
Quality RIN ≥8, No DNA contamination RIN >6, high quality total RNA
Concentration ≥200ng/ul small RNA≥334ng/ul or total RNA≥67ng/ul
Amount Total RNA 2ug small RNA 2ug or total RNA 6ug

Turnaround time

Hiseq : within 4 weeks
Ion Proton : within 3 weeks

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MeDIP-Sequencing (DNA Methylation)
Price on request

Along with structural and functional information, it has been revealed that epigenetic expression system also plays an important role in DNA transcription. Because epigenetic genome transforms and inherits depending on the environment of the organism, it is possible to lay an essential foundation for diagnosis and treatment of the... Show more »

Along with structural and functional information, it has been revealed that epigenetic expression system also plays an important role in DNA transcription. Because epigenetic genome transforms and inherits depending on the environment of the organism, it is possible to lay an essential foundation for diagnosis and treatment of the associated diseases.

MeDIP (Methylated DNA immunoprecipitation)

Method to sequence a selectively captured region through immunoprecipitation reaction by using antibody that binds to methylated cytosine.

Sample requirements

Material Amount Conc(ng/ul) Platform
ChIPed 30ng 1ng/ul Illumina HiSeq2000/2500

Turnaround time

Hiseq : within 4 weeks
Ion Proton : within 3 weeks

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ChIP-Seq
Chromatin Immunoprecipitation Sequencing
Price on request

Along with structural and functional information, it has been revealed that epigenetic expression system also plays an important role in DNA transcription. Because epigenetic genome transforms and inherits depending on the environment of the organism, it is possible to lay an essential foundation for diagnosis and treatment of the... Show more »

Along with structural and functional information, it has been revealed that epigenetic expression system also plays an important role in DNA transcription. Because epigenetic genome transforms and inherits depending on the environment of the organism, it is possible to lay an essential foundation for diagnosis and treatment of the associated diseases.

ChIP

(Chromatin immunoprecipitation Sequencing) method to see at a large scale by separating binding site of transcription factor and modification site by using immunoprecipitation reaction.

Sample requirements

Material Amount Conc(ng/ul) Platform
ChIPed 30ng 1ng/ul Illumina HiSeq2000/2500

Turnaround time

Hiseq : within 4 weeks
Ion Proton : within 3 weeks

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mRNA Sequencing
Price on request

The recent development of Next Generation Sequencing technology has allowed the production of bulk sequencing data. Whole transcriptome analysis using these bulk data not only provides the expression level between genes, but also provides the data of novel transcriptome, discovery of isoform, and fusion gene.

*RNA Sequencing... Show more »

The recent development of Next Generation Sequencing technology has allowed the production of bulk sequencing data. Whole transcriptome analysis using these bulk data not only provides the expression level between genes, but also provides the data of novel transcriptome, discovery of isoform, and fusion gene.

RNA Sequencing Summary

Application Method Feature Sequencing Platform
mRNA Selection using poly‐T oligo Strand specific Hiseq 2000/2500&Ion ProtonTM
Total RNA rRNA Depletion Strand specific mRNA and various non coding RNA (lincRNA,snRNA, snoRNA) analysis Hiseq 2000/2500&Ion ProtonTM
Small RNA Size selection(20~70bp) Separate analysis of non coding RNA and micro RNA Hiseq 2000/2500&Ion ProtonTM

Benefit

RNA-seq vs Microarray

RNA-SEQ Microarray
Production of reproducible data O O
Dynamic range 10e5 10e2
Background signal Low High
Alternative splice site check O X
Discovery of novel Isoform (Fusion) O X
Analysis of sample with no standard genomic information O X

Sample requirements

Hiseq Proton
Quality RIN ≥ 8 , No DNA contamination RIN >7, high-quality, intact RNA
Concentration ≥100ng/ul ≥100ng/ul or ≥625ng/ul
Amount Total RNA 2ug RNA 6ug

Turnaround time

Hiseq : within 4 weeks
Ion Proton : within 3 weeks

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Whole Genome Sequencing
Price on request
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Whole Exome Sequencing (WES)
Price on request

Exome Sequencing is a method that selectively analyzes only coding region (Exon), which composes 1-2% of the genome. It is a cheaper and effective way of sequencing compared to whole genome sequencing that analyzes the entire genome. Not only does it sequence single nucleotide polymorphism (SNP), but exome sequencing also... Show more »

Exome Sequencing is a method that selectively analyzes only coding region (Exon), which composes 1-2% of the genome. It is a cheaper and effective way of sequencing compared to whole genome sequencing that analyzes the entire genome. Not only does it sequence single nucleotide polymorphism (SNP), but exome sequencing also identifies insertion and deletion. Based on these analysis results, exome sequencing can be effectively used in research for rare disease, cancer genomics, and genetic disorders.

Exome Capture method

DNA Link uses various Exome Capture kits to provide Exome sequencing service.

Agilent SureSelect illumina Nextera Rapid (Expanded) Ion AmpliSeq Exom
Method Solution Hybridization Hybridization Targeted PCR
Target size 50M~75M(V3~V5+UTR) 37M (62M) 33M(~58M)
Contents Exons(+UTR) Exons(Exons, UTR, miRNA) Exons
Library Design Time 3days 1.5days 6hrs
Input DNA 1ug (3ug) 50ng 50~100ng
Sequencer Hiseq 2000/2500 Ion Proton system

Main Capture Products

  • SureSelect Human All Exon Kits (for the HiSeq Sequencer)
  • SureSelect Human All Exon V5 (targeting coding regions only) and V5+UTRs (targeting coding regions plus UTRs)
  • SureSelectXT Human All Exon 50Mb
  • SureSelectXT Human All Exon V4
  • SureSelectXT Human All Exon V4+UTRs
  • SureSelectXT Human All Exon V5
  • SureSelectXT Human All Exon V5+UTRs
  • SureSelectXT Human All Exon V5+lncRNA
  • SureSelectXT Human All Exon V5 Plus
  • Ion torrent Exome Kits (for the Ion Proton™ System)
  • Ion AmpliSeq™ Exome Kit
  • Ion TargetSeq™ Exome Enrichment : Ion-TargetSeq-Exome-50Mb-hg19

Sample requirement

platform protocol Sample Type minimum Concentration minimum volume Required Amount (including QC)
HiSeq SureSelect exomegDNA 25ng/ul(3ug) or 8.4ng/ul(1ug) 120ul 4ug or 2ug
HiSeq Truseq exome gDNA 20ng/ul 55ul 2ug
HiSeq Nextera Rapid Capture Exome gDNA 5ng/ul 10ul 500ng
HiSeq Nextera Rapid Capture Expanded Exome gDNA 5ng/ul 10ul 500ng
Proton SureSelect(modify) gDNA 8.4 ng/μL 120ul 2ug
Proton LT exome gDNA 8.4 ng/μL 120ul 2ug
Proton AmpliSeq Exome gDNA 4.8ng/ul 21ul 1ug

Turnaround time

platform Illumina HiSeqAgilent SureSelect Ion ProtonTM IonAmpliSeq Exome
Run Info 2x100 Paird End Ion PITM Chip(v2)
Time for Experiment * Based on production of raw data 6 weeks 2 weeks
  • The time is based on the production of raw data, and may be adjusted depending on the number of samples.
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Agilent SureSelect
Ion AmpliSeq
Illumina Nextera
De Novo Genome Sequencing
Price on request

De Novo sequencing sequences the whole genome sequence of unidentified microorganisms or animals and plants, and genetic factors of sarcoma and disorders can be discovered from the obtained results. By utilizing both the short read from Illumina Hiseq and long read from DNA Link’s Pacbio RS II, we provide service optimized for... Show more »

De Novo sequencing sequences the whole genome sequence of unidentified microorganisms or animals and plants, and genetic factors of sarcoma and disorders can be discovered from the obtained results. By utilizing both the short read from Illumina Hiseq and long read from DNA Link’s Pacbio RS II, we provide service optimized for genome assemble finishing.

Benefit

In De Novo assemble, long reads have an advantage of creating long contigs from having many long read composition, and Pacific Biosciences SMRT (Single Molecule Real Time) RS, which is a third generation sequencer, also has an advantage of ability to read at length a single molecule in real time without the amplification step. Long reads allow to overcome repeat and GC rich region, and obtain single contig. In addition, it is also possible to obtain an optimal outcome by performing a hybrid assembly between long reads and short reads and adjusting error and accuracy accordingly.

  • scaffolding of large genomes
  • Longest read lengths with over 20,000 bp observed
  • Greater than 99.999% (QV 50) accurate sequencing
  • Sensitivity to detect minor variants at frequency less than 0.1%
  • No amplification bias and least impacted by GC content
  • Coverage uniformity
  • Shortest run time
  • De Novo Assembly: Reduce Ambiguities
  • Complete microbial genomes and improve assemblies of larger organisms
  • Read lengths up to 20kb, unbiased genome coverage, and high accuracy

Sample requirements

  • sample quantity required :
    • short-insert libraries: ≥3 µg
    • Large-insert libraries: ≥20 µg
  • sample concentration :
    • short-insert libraries: ≥ 40ng/ul
    • Large-insert libraries: ≥ 200ng/ul
  • sample quality : A260/280:1.8-2.0, A260/230: ≥ 1.8 , Intacted DNA, RNA-free DNA, non-degraded

Turnaround time

About 4 weeks

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SMRT Sequencing
Single Molecule Real-Time Sequencing
Price on request
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PacBio RS II
Targeted Resequencing
Price on request

Target Resequencing analyzes sequence of only the targeted region from the entire genomic DNA. The method is universally used in analyzing data of Genome Wide Association Study (GWAS) and selectively obtaining genomic region of specific disease. Methods such as, Capture, long range PCR, and multiplex PCR are often used in securing... Show more »

Target Resequencing analyzes sequence of only the targeted region from the entire genomic DNA. The method is universally used in analyzing data of Genome Wide Association Study (GWAS) and selectively obtaining genomic region of specific disease. Methods such as, Capture, long range PCR, and multiplex PCR are often used in securing sequence of target region, and appropriate method should be selected based on the number of samples and the size of target region.

Benefit

Able to design probe or primer pool for the region of interest as a way of capturing selected target.
- Provides capture service from various platforms of NimbleGen, Agilent, and Ion torrent.
- Able to provide customized service by using various NGS Sequencer of HiSeq, 454, PGM, Ion Proton, and PacBio.

Turnaround time

HiSeq : 3 weeks
454 : 3 weeks
Ion Proton, PGM : Ampliseq < 10 sample : 2 weeks, Ampliseq ≥ 10 sample : 3 weeks
Pacbio : 2 weeks

Sample requirement

platform protocol Sample Type minimum Concentration minimum volume Required Amount (including QC)
HiSeq SureSelect targeted gDNA 25ng/ul(3ug) or 8.4ng/ul(1ug) 120ul 4ug or 2ug
HiSeq Nextera Rapid Capture Custom Enrichment gDNA 5ng/ul 10ul 500ng
HiSeq TruSight Cancer gDNA 5ng/ul 10ul 500ng
HiSeq TruSight Cardiomyopathy gDNA 5ng/ul 10ul 500ng
Hiseq TruSight Inherited Disease gDNA 5ng/μL 10ul 500ng
HiSeq TruSight Autism gDNA 5ng/ul 10ul 500ng
454 Amplicon(fusion primer) gDNA 10ng/uL 100ul 1ug
454 Amplicon(library prep) amplicon 32ng/uL 16ul 1ug
Proton SureSelect(targeted) gDNA 84ng/ul 120ul 2ug
Proton LT targeted gDNA 84ng/ul 120ul 2ug
Proton Fragment library(amplicon) gDNA or amplicon 3.4 ng/ul or 6ng/ul 6ul or 50ul 500ng
Proton amplicon(fusion primer) amplicon 12.5 ng/ul 4ul 500ng
Proton cancer panel v2 gDNA 1.7 ng/μL 6ul 500ng
Proton CCP(Comprehensive cancer panel) gDNA 17ng/ul 6ul 500ng
Proton IDP(Inheritied Disease panel) gDNA 17ng/ul 6ul 500ng
PGM Fragment library(amplicon) gDNA or amplicon 3.4 ng/ul or 6ng/ul 6ul or 50ul 500ng
PGM Fragment library(amplicon)<350bp gDNA or amplicon 12.5ng/ul or 2.9ng/ul 4ul or 35ul 500ng
PGM Fragment library(amplicon)>400bp gDNA or amplicon 12.5ng/ul or 6ng/ul 4ul or 50ul 500ng
PGM amplicon(fusion primer) gDNA 12.5ng/ul 4ul 500ng
PGM cancer panel v2 gDNA 1.7ng 6ul 500ng
Pacbio amplicon (250bp~2kb) amplicon 50ng/ul 21ul 3ug
Pacbio amplicon (5kb~10kb) amplicon 200ng/ul 30ul 10ug
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Equipment
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Biology
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Biochemistry & Molecular Biology
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Biomolecular Interaction Analysis
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Protein-DNA Interaction Analysis
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Chromatin Immunoprecipitation (ChIP) Assays
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Nucleic Acid Services
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DNA Services
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Genotyping Services
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DNA Sequencing
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Next Generation Sequencing (NGS)
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Targeted Gene Sequencing
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Exome Sequencing Services
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Epigenetic Studies
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PCR
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DNA Hybridization
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RNA Services
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RNA Sequencing
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Pharmacology & Toxicology
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Bioanalysis
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Biomarkers
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