Whole-Genome Sequencing (WGS)
Explore single-nucleotide variants, insertions, deletions and other suitable variant classes across the genome.
Service atlas · 19 research services
Browse six research categories and an integrated personal genetics page. Filter by category or keyword, then open any service for full details.
19 research services + personal genetic testing (four products on one page)
Showing 20 services
Explore single-nucleotide variants, insertions, deletions and other suitable variant classes across the genome.
Enrich exonic regions by targeted capture to investigate protein-coding variation.
Quantify gene and transcript expression to investigate differential expression, alternative splicing and functional pathways.
Investigate cell composition, heterogeneity, states and developmental trajectories at single-cell resolution.
Use template-switching amplification to investigate full-length transcripts from single cells or low-input RNA.
Use Tn5 transposase to profile accessible chromatin and compare accessibility across biological states.
Enrich DNA bound by a target protein to investigate transcription-factor binding and histone modifications.
Use antibody-guided transposition to map target chromatin proteins and histone modifications.
Map DNA methylation at single-base resolution using bisulfite conversion and sequencing.
Enrich CpG-rich regions to investigate DNA methylation using a focused sequencing strategy.
Enrich methylated DNA using antibodies to compare regional methylation signals.
Enrich RNA fragments using m6A-specific antibodies to investigate transcriptome-wide RNA methylation.
Use RNA immunoprecipitation to identify RNAs associated with a target RNA-binding protein.
Combine crosslinking, immunoprecipitation and sequencing to map RBP-binding regions and sequence preferences.
Select tissue regions by laser-capture microdissection and retain spatial origin through omics profiling.
Capture spatial chromatin interactions to study three-dimensional genome organization and condition-specific changes.
Integrate transcriptomic, chromatin and DNA methylation sequencing data to investigate cross-omics regulatory relationships.
Identify and quantify proteins using mass spectrometry to investigate composition and abundance changes.
Compare metabolic profiles or quantify a predefined set of target metabolites.
Explore Yuerkang, Yunerbao, Health Guardian and the VIP Package, with full service descriptions and retail prices on one page.
Start your project
Discuss samples, key comparisons and analysis objectives with our project team.