Services
From study design and quality control to statistical interpretation, visualization, and manuscript support.
What we offer
End to end scRNA-seq (10X Genomics, Smart-Seq2) and spatial transcriptomics (10X Visium/VisiumHD, MERFISH) analysis including quality control, integration, cell type annotation, trajectory analysis, cell-cell communication, and multi sample integration.
View pipelineComprehensive bulk RNASeq data analysis, from raw sequencing reads to actionable biological insights, including quality control, differential expression, co-expression networks, and pathway interpretation.
View pipelineAdvanced whole genome and exome sequencing analysis, from raw data processing to accurate variant detection, annotation, and interpretation, enabling meaningful clinical and research insights.
View pipelineTurn high-dimensional protein measurements into clear biological findings through assay and sample quality control, differential protein abundance testing, pathway analysis, biomarker evaluation, and integration with clinical or other omics data.
View pipelineMap transcription-factor binding and histone modifications with a reproducible workflow covering read quality control, alignment, enrichment assessment, peak calling, differential binding, motif discovery, and regulatory interpretation.
View pipelineAnalyze Illumina EPIC and 450K methylation arrays from raw IDAT files through sample and probe quality control, normalization, batch assessment, differential methylation, region analysis, and pathway interpretation.
View pipelineSupervised and unsupervised learning applied to biological data, classification, regression, clustering, deep learning for protein sequences, and multi-omics integration.
Discuss this serviceCustom R Shiny dashboards and interactive multi omics visualization webtools for exploring and sharing complex genomic datasets with collaborators and clinicians.
Discuss this serviceEngagement model
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