OMAPiX delivers end-to-end multiomics services built around your scientific question.
01 / Single Cell
We deliver end-to-end single-cell sequencing services to help you resolve cellular heterogeneity, identify rare cell populations, and track dynamic cell states.

Up to 20,000 cells per sample. 3′, 5′, immune profiling, ATAC, multiome, fixed RNA, and nuclei applications. Compatible with CITE-seq and hashing.
Combinatorial barcoding for whole transcriptome and immune profiling. Scale to 5 million cells in a single assay. Fixation-stable for flexible sample handling.
Microwell-based capture up to 80% efficiency. Supports protein detection, ATAC, and multiplexing. Embedded QC scanner.
Whole-transcriptome spatial profiling at 2µm resolution. 6.5mm² or 11mm² capture areas. Compatible with fresh frozen and FFPE.
Subcellular resolution in situ spatial transcriptomics. Up to 5,000-plex RNA and protein detection. Two 12x24mm capture areas per run.
High-resolution whole-transcriptome spatial mapping at 10µm resolution. Fresh frozen, organism-agnostic.
Integrated sequencing and in situ multiomic analysis. Cytoprofiling of up to 1 million cells in under 24 hours — capturing morphology, RNA, protein, and in situ sequencing in a single workflow.
02 / Spatial Biology
Map gene and protein gene expression localization directly within tissue architecture. We support leading spatial platforms to deliver subcellular resolution.

03 / Sequencing
From standard RNA-Seq to ultra-deep whole genome sequencing, our platform-agnostic sequencing services deliver rapid turnaround and industry-leading data quality.

Highest in class quality scores. Up to 2×300bp reads. Optimized for accuracy-sensitive applications.
Up to 25 billion reads. DRAGEN-compatible pipelines.
Whole transcriptome, mRNA-seq, and targeted RNA profiling to capture gene expression dynamics and splicing variants.
Whole genome sequencing (WGS), exome sequencing (WES), and targeted panels for comprehensive variant detection and genomic mapping.
Assay for Transposase-Accessible Chromatin to map chromatin accessibility and resolve epigenomic regulation across samples.
04 / Bulk Genomics
Comprehensive DNA, RNA, and ATAC sequencing workflows tailored to resolve complex genomic, transcriptomic, and epigenomic questions.
