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RESEARCH SERVICES
M.D./Ph.D. 전문가 인력으로 구성된 지놈인사이트 리서치팀은 글로벌 수준의 빠르고 정확한 NGS 기술력으로 정밀의학 연구에 새로운 통찰력을 제공합니다.
Group 37707
Group 38002
Research Services
Whole Genome Sequencing
Epigenetics and Immune Profiling
Transcriptome Sequencing
Single Cell Multi-omics Sequencing
Whole Genome Sequencing
Whole genome de novo sequencing:
Our de novo sequencing accurately characterizes any species without a reference sequence available for alignment.
Whole genome re-sequencing:
Our WGS process provides a comprehensive analysis of the genome, including SNVs, insertions & deletions, CNVs, and SVs,using a reference genome. This information can be used to discover candidate genes associated with disease and drugresponse, enabling personalized precision medicine.
Sequencing platform and product
Sequencing platform
NovaSeq 6000 Sequencing System, Illumina
Library Prep
TruSeq PCR-free Nano, Illumina
글로벌 수준의 NGS 연구 서비스를 지금 경험해보세요. 지놈인사이트의 리서치 팀이 빠르고 정확한 NGS 분석 기술과 노하우를 기반으로 연구 과제를 함께 계획하고 과제의 목표 달성을 위해 함께 나아갑니다.
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Epigenetics and Immune Profiling
Human Leukocyte Antigen (HLA):
Accurate and cost-effective HLA typing with our NGS-based approach, performed by experienced scientists and technicians committed to quality outcomes. Trust us to meet your program requirements with fast, reliable results.
Chromatin-immunoprecipitation (ChiP):
Unlock insights into protein-DNA interactions and histone modifications across the genome with our ChiP-Seq services. Benefit from our expertise in ChiP assays, sonication optimization, and bioinformatics, and obtain high-quality data for your research.
TCR/BCR Bulk Sequencing:
Our repertoire sequencing services use NGS technology to accurately detect and analyze T and B cell repertoires for both bulk and single cell analysis. Gain insights into the immune system's fundamental processes in healthy individuals and uncover mechanisms behind autoimmune diseases, allergies, cancer, and aging.
글로벌 수준의 NGS 연구 서비스를 지금 경험해보세요. 지놈인사이트의 리서치 팀이 빠르고 정확한 NGS 분석 기술과 노하우를 기반으로 연구 과제를 함께 계획하고 과제의 목표 달성을 위해 함께 나아갑니다.
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Transcriptome Sequencing
mRNA/ Total RNA sequencing:
Our RNA sequencing service, utilizing NGS technology, provides precise and sensitive measurement of gene expression levels across transcriptomes. With our service, you can detect changes caused by disease, treatment response, and environmental factors, gaining insight into gene-enabled research and expression control. We also offer detection of novel transcriptomes, fusion genes, alternative splicing, and mutations, providing a comprehensive view of gene regulation and expression control for research in biomarker development, disease diagnosis, and monitoring.
Sequencing platform and product
Sequencing platform
NovaSeq 6000 Sequencing System, Illumina
Library Prep
TruSeq Stranded Total RNA,
Illumina/KAPA Hyper RNA, Roche
글로벌 수준의 NGS 연구 서비스를 지금 경험해보세요. 지놈인사이트의 리서치 팀이 빠르고 정확한 NGS 분석 기술과 노하우를 기반으로 연구 과제를 함께 계획하고 과제의 목표 달성을 위해 함께 나아갑니다.
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Single Cell Multi-omics Sequencing
Single cell RNA sequencing:
Our scRNA-seq services use NGS technology to analyze gene expression in individual cells, enabling the study of complex cell processes and the identification of cellular heterogeneity and rare cell populations. Unlike bulk RNA sequencing, which provides average values by combining various cells, ScRNA-seq separates a group of cells into single cells for analysis. This approach is particularly valuable for investigating live tissues, which are composed of diverse cell types with unique functions and heterogeneity between subpopulations of cells.
Single nucleus RNA sequencing:
Our single cell nucleus RNA sequencing technology overcomes limitations in analyzing sensitive cells that are easily damaged or difficult to separate. By analyzing the transcriptome of a single nucleus, this method eliminates stress and bias that may occur during single cell separation. Unlike scRNA-seq, which works best with fresh tissue samples, single cell nucleus RNA sequencing allows for analysis of frozen samples and transcription from tissues that are difficult to separate.
Single cell immune profiling (TCRs, BCRs):
Our single cell immune profiling services utilize VDJ and VJ gene sequencing to analyze the diversity of clonotypes at the single cell level, allowing for precise immune profiling of T cell receptors and B cell receptors.
Single cell ATAC sequencing:
Our single cell ATAC sequencing technique uses transposase to assess genome-wide chromatin accessibility by inserting sequencing adapters into open chromatin regions. This approach analyzes the DNA release information in a single nucleus while mapping binding sites of transcription factors and nucleosome locations. By identifying cell-specific binding sites and activity of transcription factors, researchers can gain insights into cell-specific functions when analyzing a single cell.
Sequencing platform and product
Sequencing platform
NovaSeq 6000 Sequencing System, Illumina
Library Prep
Chromium Single Cell Solution,
10x Genomics
글로벌 수준의 NGS 연구 서비스를 지금 경험해보세요. 지놈인사이트의 리서치 팀이 빠르고 정확한 NGS 분석 기술과 노하우를 기반으로 연구 과제를 함께 계획하고 과제의 목표 달성을 위해 함께 나아갑니다.
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샌디에고
6330 Nancy Ridge Drive,
Suite 106,
San Diego, CA 92121
(858)-665-2120
서울
서울시 서초구 
서운로 20, 4층 
(서초동, 효봉빌딩) 
(우: 06734)
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대전
대전광역시 유성구
문지로 193, 진리관 T331
(문지동, KAIST 문지캠퍼스) (우: 34051)
 
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홍콩
RD11, 133 Wai Yip Street
Kwun Tong,
홍콩
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