Skip to main content

Next-Generation Molecular Diagnostics, Made Simple.

NGS-Driven Clarity for Embryo Viability

Take control of your preimplantation genetic testing for aneuploidy (PGT-A) workflow with EVASEQ’s all-in-one library kit and cloud portal. Designed for fertility clinics and genetic labs, EVASEQ simplifies NGS-based embryo screening so you can bring testing in-house — reducing turnaround time, lowering cost and improving clinical control.

About Evaseq

Evaseq is a research-driven biotech solutions company focused on transforming molecular diagnostics through innovation, quality assurance, and customer-centric design. Our mission is to enable every clinic and laboratory to perform high-quality genetic testing independently—without relying on external labs.

With validated NGS-based kits, robust workflows, and intuitive analytics software, Evaseq supports genetic testing workflows including PGT-A, PGT-M, PGT-SR, NGS library prep, and molecular research assays.

Key Features

Benefits & Value Proposition

Faster turnaround

No need to outsource; results stay within your facility

Cost-efficient

Lower per-sample cost compared to third-party reference labs

Clinical control

Ownership over your data and workflow, aligning with your brand and patient-experience standards

Scalable

Start with low volumes and scale as your program grows

Data transparency

Portal empowers your team with QC metrics, sample history, and audit trails

Better patient experience

Quicker decisions, improved communication, and reduced embryo-holding time

Technical Overview

  • Input – Single-embryo biopsy or trophoectoderm sample; minimal DNA input required.
  • Library prep – Library preparation kit includes reagents for whole-genome amplification (if required), fragmentation, end-repair, adapter ligation, indexing and cleanup.
  • Sequencing – Compatible with Nanopore, Thermofisher, Illumina for aneuploidy detection.
  • Portal analytics – After upload of FASTQ/BAM, the portal runs QC (mapping %, duplication rate, coverage uniformity), then runs aneuploidy detection algorithm. Generates PDF report, interactive dashboard and data export.
  • Compliance & traceability – Sample barcoding, audit trail, user-access management. Lab maintains control of raw data and final clinical report.
  • Support – Includes workflow guide, reagent specifications, sequencing recommendations, troubleshooting guide, and hot-line/email support.
Use Case

Clinic & Lab Workflow

1

A couple undergoes IVF with embryo biopsy on day 5/6.

2

The embryologist loads the biopsy material into the EVASEQ library kit and follows the workflow.

3

Libraries are pooled and sequenced overnight on your in-house sequencer or via your preferred service.

4

Raw data is uploaded (or streamed) to EVASEQ portal. The system processes it, generates ploidy calls, QC flags, and a clinician-friendly report.

5

The embryology team reviews the report, selects euploid embryos and proceeds with transfer or cryopreservation.

6

The portal archive allows long-term tracking, retrospective review, and integration with your EMR/IVF-suite.

Why EVASEQ?

At EVASEQ, we believe clinics and labs should own the testing process—not outsource it. With decades of experience in genetics and diagnostics, our team developed a robust kit + portal platform that blends ease-of-use with clinical-grade performance. Whether you’re just launching an in-house PGT-A program or expanding volume, EVASEQ offers the flexibility, transparency and control you
need.

Reinventing Molecular Diagnostics for IVF & Genetic research capabilities!

Evaseq delivers state-of-the-art molecular diagnostics kits and software solutions that empower laboratories and fertility clinics to run advanced genetic tests with unmatched accuracy, transparency, and efficiency. From PGT-A library prep kits to our integrated bioinformatics platform, Evaseq is redefining how clinics adopt and scale next-generation sequencing workflows.

Close Menu