| Service | Typical analyst effort | Example outputs |
| Bulk RNA-seq Analysis | From 3 working days | QC summary, alignment/quantification metrics, differential expression analysis, pathway/enrichment analysis, plots and results tables |
| Single-cell RNA-seq Analysis | From 4–5 working days | Cell-level QC, filtering, clustering, marker gene analysis, cell type annotation support, integration and visualisation |
| Spatial Transcriptomics Analysis | From 3 working days | Spatial QC, normalisation, clustering, spatial feature plots, gene expression visualisation and summary report |
Explore our bioinformatics analysis workflows across genomics, transcriptomics, epigenomics, cancer genomics and multi-omics. Each workflow includes indicative analyst effort and example outputs to help researchers plan their projects.
Transcriptomics
Epigenomics
| Service | Typical analyst effort | Example outputs |
| ChIP-seq Analysis | From 3 working days | QC, alignment, peak calling, annotation, differential binding analysis and summary plots |
| CUT&RUN Analysis | From 3 working days | QC, alignment, peak calling, signal profiling, annotation and visualisation |
| ATAC-seq Analysis | From 3 working days | QC, alignment, peak calling, chromatin accessibility analysis, motif/annotation support and visualisation |
DNA Methylation
| Service | Typical analyst effort | Example outputs |
| Bisulfite Sequencing / Methylation Analysis | From 3 working days | QC, methylation calling, differential methylation analysis, genomic annotation and summary plots |
Germline Genomics
| Service | Typical analyst effort | Example outputs |
| Panel, WES or WGS Singleton/Trio/Family-based Analysis | From 5 working days | QC, variant calling or review, annotation, filtering, inheritance-based prioritisation and candidate variant tables |
| Long-read WGS Singleton/Trio/Family-based Analysis | From 5 working days | Long-read QC, alignment, SNV/indel and structural variant analysis, annotation and prioritisation |
| Rare Disease Variant Prioritisation | By scoping; typically from 3–5 working days | Phenotype-driven filtering, candidate gene/variant review, inheritance model assessment and prioritised variant lists |
Cancer Genomics
| Service | Typical analyst effort | Example outputs |
| Somatic Tumour-only or Tumour-normal Panel/WES/WGS Analysis | From 5 working days | QC, somatic variant calling, annotation, tumour-normal comparison where applicable, summary tables and visualisations |
| Long-read Somatic Tumour-only or Tumour-normal WGS Analysis | From 5 working days | Long-read QC, structural variant analysis, somatic variant detection support, annotation and reporting |
| Circulating Tumour DNA Analysis | From 5 working days | ctDNA QC, variant detection, allele fraction summaries, longitudinal or comparative analysis where applicable |
Massively Parallel Reporter Assay (MPRA) data analysis
| Service | Typical analyst effort | Example outputs |
| MPRA data analysis | From 3 working days | Count tables for candidate reporter sequences, QC reports |
Multi-omics
| Service | Typical analyst effort | Example outputs |
| Multi-omics Data Integration | From 5 working days | Integration of genomic, transcriptomic, epigenomic or clinical datasets; correlation analysis; pathway-level interpretation; visual summaries |
| Cohort-level Comparative Analysis | From 5 working days | Group comparisons, cohort stratification, statistical modelling, summary graphics and results tables |
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