Archive Gating
Assess FFPE tissue preservation and intact nuclei to screen eligible retrospective cohorts.

✦ 01 / CONTINUOUS WORKFLOW
Arc·ell seamlessly pairs archival pathology, same-cell multi-omics, and evolutionary analytics so every study unlocks defensible conclusions from retrospective patient histories.

Engineered backwards from critical biological questions to preserve cell identity.
The platform addresses the pivotal checkpoints that determine single-cell oncology success: strict archival tissue QC, high-throughput in situ nanowell library preparation, direct same-cell multi-omics pairing, and lineage-aware phylogenetic reconstruction.
Each module operates independently or combines into an end-to-end evidence trajectory from clinical specimen to published mechanism.
Assess FFPE tissue preservation and intact nuclei to screen eligible retrospective cohorts.
Generate high-resolution genome-wide copy number profiles from archival samples via Arc-well.
Read DNA copy number and 3' RNA from the identical microwell using wellDR-seq chemistry.
Trace tumor phylogenies, clonal seeding, and therapy-resistant subclone dynamics.
Before sequencing the first cell, we align on quality gates, cohort inclusion criteria, and mechanistic hypotheses.
Consult Study Design →Clarify tumor origin, primary-to-metastasis evolution, therapy selection, or genotype-to-phenotype regulation.
Select Arc-well for large-cohort CNA tracking or wellDR-seq for same-cell multi-omics mechanistic depth.
Run a pilot cohort of 3–5 representative specimens with strict gating (GO / HOLD / STOP) to de-risk full study scaling.