RNA-Seq Analysis
Bulk transcriptomics with DESeq2/edgeR, QC, alignment and pathway enrichment.
From experimental design to scalable cloud delivery — pick a service or compose a full omics program.
Bulk transcriptomics with DESeq2/edgeR, QC, alignment and pathway enrichment.
10x Chromium, Seurat & Scanpy workflows, integration and trajectory analysis.
Visium / Xenium / MERFISH analysis, niche detection, cell–cell interaction.
Orthology, synteny, evolutionary models across species and strains.
Shotgun & 16S microbiome analysis with taxonomic and functional profiling.
QC, imputation, association testing and polygenic risk scoring.
Neuronal vulnerability mapping, multi-omics integration and single-cell brain atlases for neurodegeneration research.
Reproducible Nextflow / Snakemake stacks with CI/CD and containers.
Study design, statistical strategy and reviewer-ready interpretation.
End-to-end omics pipelines tailored to your data and infrastructure.
AWS / GCP / Azure HPC, batch, S3, Terraform and cost optimization.
Hands-on workshops on NGS, scRNA-seq, R/Python and reproducibility.