01
Genomics
Investigate genetic variation and candidate mechanisms with whole-genome and whole-exome data.
Whole-Genome Sequencing (WGS) · Whole-Exome Sequencing (WES)Explore these servicesSequencing · Bioinformatics · Multi-omics
Every sequence,closer to an answer
Research services connecting sample preparation, library construction, sequencing and bioinformatics to study gene regulation, cell states and disease mechanisms.
For research institutions, hospitals and biopharmaceutical companies
>10 yearsOmics and R&D technical services
ConnectedSamples · Libraries · Sequencing · Analysis
Multi-omicsSpatial · Expression · Regulation · Metabolism
AI-enabled throughoutDesign · Deep analysis · Prediction
Research services
Start with a question.
Find the right approach.
Choose suitable methods across six research categories and bring complementary omics evidence to a shared question.
02
Transcriptomics & Single Cell
Explore tissue expression, cellular heterogeneity and expression from low-input samples.
RNA Sequencing (RNA-Seq) · Single-Cell Transcriptomics · SMART-SeqExplore these services03
Epigenetics
Study regulation through chromatin, DNA and RNA modifications 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-SeqExplore these services04
Spatial & Multi-omics
Connect spatial origin, three-dimensional organization and sequencing-based multi-omics evidence.
LCM Spatial Multi-omics · Hi-C Sequencing · Integrated Multi-omics Analysis (Sequencing Projects)Explore these services05
Proteomics
Explore protein abundance, function and pathways beyond transcription.
ProteomicsExplore these services06
Metabolomics
Investigate metabolite and pathway changes with targeted and untargeted measurements.
Targeted / Untargeted MetabolomicsExplore these servicesFrom sample to insight
Connect experiments and analysis
from the start.
Study design
Define the question, samples, groups and analysis objectives.
Samples and libraries
Select the laboratory workflow and assess sample and library quality.
Measurement and analysis
Generate sequencing or omics data, process results and perform statistical analysis.
Result discussion
Interpret findings in context and discuss follow-up validation.
Research stories
News and research
NSD2 and epigenetic regulation of ferroptosis in skin cells
RNA sequencing and CUT&Tag connect NSD2, histone signals and ferroptosis in keratinocytes.
Read the story
Single-cell and epigenomic insights into adipose hyperplasia in port-wine stains
Cell populations, chromatin accessibility and expression data inform investigation of SPSB1 and HDAC1.
Read the story
Copper–caffeic acid nanozyme: transcriptomic clues to cell-death mechanisms
RNA sequencing and pathway analysis support investigation of the nanozyme’s cellular effects.
Read the storyAbout Genefund
Connecting experiments and data
Genefund brings together Jingmai Biotech and its wholly owned Shanghai subsidiary, Jingfang Biotech, to provide sequencing and omics research services for universities, medical institutions and biotechnology companies. The team combines genetics, genomics, informatics, statistics and computer science, connecting sample preparation and library development with sequencing and bioinformatics.
Meet our company and teamStart your project
Have samples, or the start of an idea?
Tell us about your research system, samples and question. We can discuss a suitable technical plan.