Sequencing services.
Choose 10x single-cell sequencing, RNA-seq, shotgun metagenomics, or WGS with practical help on sample handling, sequencing depth, QC, downstream analysis, and read-based project scoping.
10x Single Cell Sequencing
Uncover rare populations, immune states, and developmental trajectories with on-site freshness support for time-sensitive single-cell work.
- On-site handoff, fast transfer, and lab intake coordination
- Cell-by-cell transcriptomic resolution
- Clustering, annotation, and differential expression
RNA-seq
Measure expression programs, treatment responses, splice variants, and pathway-level changes without overbuying sequencing depth.
- Flexible service scoped by the reads your study needs
- Read-based pricing instead of read-length or fixed-batch pressure
- Gene and isoform-level analysis
Shotgun Metagenomics
Move from organism detection to functional capacity, resistance profiling, and strain-aware microbiome analysis.
- Taxonomic and functional profiling
- AMR and virulence factor detection
- Flexible databases and custom analysis options
Whole-Genome Sequencing
Sequence research genomes with coverage-aware planning, QC expectations, and downstream variant-ready outputs.
- WGS planning around target coverage and species
- Library QC and sequencing coordination
- Analysis support for study-specific outputs
More than standard catalog work.
The Athenomics service menu also supports 16S/ITS, antibody sequencing, CRISPR screens, custom sequencing, tissue dissociation, nuclei extraction, library QC, and lane-level sequencing capacity.
Sequencing-only support
PE150 extra sequencing, custom read-depth planning, and small jobs scoped by reads rather than lane minimums.
Antibody sequencing
Hybridoma sequencing, display library work, single B cell projects, and BCR/TCR options for immune studies.
CRISPR and specialty workflows
Custom sequencing and bioinformatics support for study-specific assays that do not fit a standard catalog page.
Fast handoff, flexible scale, clear answers.
Athenomics is positioned for researchers who want the convenience of a modern sequencing service with the care of a scientific collaborator and pricing matched to their read-depth needs.