New data
from old samples

A pioneering process to enable Whole Genome Sequencing from FFPE samples by extracting high quality DNA

Download datasheet

98% genome coverage
from FFPE samples

Unlock new insights from tumor samples with 98% sequence alignments covered at a depth of 20x. This process produces reliable, high-quality results for whole genome, exome, or multi-omic analysis comparable to fresh frozen-derived data, enabling quality mutation and copy number variation analyses.


Unlock novel insights, develop more targeted therapies, and speed time to value with SeqPlus.

Results comparable to fresh frozen

Generates sequence alignments covering 98% of the genome at a depth of 20x or greater, when sequenced at a depth of 70x for whole genome sequencing.

WGS from FFPE samples

Unlike traditional FFPE sequencing processes, ours can isolate enough high-quality DNA to achieve good coverage across whole genome or whole exome sequencing.

CNV analysis

Allows for high-quality mutation and copy number variation analysis.

Add sequencing to your current work flow

In addition to pathology, you can now add whole genome and whole exome sequencing to your workflow.

Proven using 15 year old archival tissue

Our assay works with archival tissue biobank samples as old as 15 years, routine clinical processing of samples for clinical trial recruitment, and tissue sections as part of normal clinical diagnostic workflows.

Salvage your degraded samples

Our FFPE process can work on specimens with degraded DNA, cross-linked nucleic acids, and low quantities of material.