Genomics
Whole-genome and exome sequencing to identify genetic variants and investigate their biological relevance.
Whole-Genome Sequencing (WGS) · Whole-Exome Sequencing (WES)View related servicesSequencing · Multi-omics · Bioinformatics
Sequencing, multi-omics and bioinformatics services for research in gene regulation, cell states and disease biology. Integrated experimental and analytical support, from study design to interpretation.
Research services
Explore complementary technologies across six research areas, with experimental design and analysis built around your study.
Whole-genome and exome sequencing to identify genetic variants and investigate their biological relevance.
Whole-Genome Sequencing (WGS) · Whole-Exome Sequencing (WES)View related servicesBulk, single-cell and low-input RNA sequencing to resolve expression patterns and cellular heterogeneity.
Transcriptome Sequencing (RNA-seq) · Single-Cell RNA Sequencing · SMART-seqView related servicesChromatin, DNA and RNA assays to investigate gene regulation and molecular interactions.
ATAC-seq · ChIP-seq · CUT&Tag · Whole-Genome Bisulfite Sequencing (WGBS) · Reduced Representation Bisulfite Sequencing (RRBS) · MeDIP-seq · MeRIP-seq (m6A-seq) · RIP-seq · CLIP-seqView related servicesSpatial profiling, genome organization and integrated omics to connect molecular findings with biological context.
Laser Capture Microdissection (LCM) Spatial Omics · Hi-C Sequencing · Integrated Multi-omics AnalysisView related servicesProtein profiling and pathway analysis to investigate biological function.
ProteomicsView related servicesTargeted and untargeted metabolite profiling to study metabolic changes and pathways.
Targeted & Untargeted MetabolomicsView related servicesFrom sample to insight
Define research goals, sample requirements, experimental groups and analysis priorities.
Select library and assay workflows for the sample type, with quality checks at key steps.
Generate sequencing or omics data, then process and analyze the results.
Review findings in biological context and identify next steps for validation.
Research stories

RNA-seq and CUT&Tag help researchers examine how NSD2 and histone modifications relate to ferroptosis in keratinocytes.
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Single-cell, chromatin accessibility and gene expression data support research into SPSB1, HDAC1 and changes in subcutaneous adipose tissue.
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RNA-seq and pathway analysis help researchers investigate the cell-death processes associated with a biomimetic nanozyme.
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By integrating multi-omics data with functional validation, this study elucidates the role of the Fas/DR5-Caspase-8 signaling axis in maintaining treatment-induced senescence, thereby pointing the way toward the development of IAP antagonists as novel senescent cell eliminators.
Read the storyAbout GENEFUND
GENEFUND provides high-throughput sequencing and omics services for universities, research institutes, medical institutions and biopharmaceutical companies. Our Suzhou team and wholly owned Shanghai subsidiary bring together expertise in genetics, genomics, bioinformatics, statistics and computer science. From sample preparation and library construction to sequencing and data analysis, our laboratory and bioinformatics teams work together throughout each project.
About GENEFUNDStart your project
Tell us about your samples and research goals. Our team will help you choose the right approach.