OASIS LAB

Reliability supported by our own laboratory.

OASIS operates genetic testing through its own laboratory and is developing a high-throughput testing laboratory in Fukuoka. We focus on direct workflow management and close coordination with medical institutions.

A professional working in a testing laboratory

LABORATORY PLATFORM

From our current laboratory to a high-throughput platform in Fukuoka.

OASIS manages genetic testing and analytical workflows through its own laboratory. Direct operational responsibility, rather than relying solely on third-party outsourcing, is a core part of how we approach testing reliability.

In Fukuoka, we are developing a high-throughput testing laboratory. Equipment, people and quality-management processes are being prepared for a domestic workflow covering specimen receipt, preparation, analysis and reporting.

LABORATORY ROADMAP

Current operations and the Fukuoka programme

OWN LAB / IN OPERATION
OASIS OWN LAB

OASIS Laboratory

An OASIS-operated laboratory for genetic testing and analysis, with designated specimen transport and management workflows.

  • Next-generation sequencing-based analysis
  • Bioinformatics
  • Preparation of test reports
UNDER DEVELOPMENT
FUKUOKA

Fukuoka High-throughput Laboratory

A domestic testing platform under development, designed around standardised workflows and scalable specimen processing.

  • Domestic specimen receipt, preparation and analysis
  • Automation-oriented high-throughput processing
  • Coordination with medical institutions in Japan
  • Connections to training and research and development

LABORATORY PROCESS

Equipment planning for automation and standardisation

Each stage from specimen receipt and preparation to nucleic-acid extraction and sample preparation is designed with standardisation and automation in mind.

An automated specimen-processing line
01Specimen receipt and automated preparation
A specimen identification and aliquoting system
02Identification and aliquoting
A nucleic-acid extraction and purification system
03Nucleic-acid extraction
A sample-preparation workstation
04Sample and library preparation

QUALITY MANAGEMENT

How we approach the testing workflow

Identity, process records and quality indicators are reviewed from specimen receipt through reporting to support consistent information for medical institutions.

01

Receipt and verification

Request data, specimen identity and condition on receipt are checked and recorded.

02

Pre-analytics and quality review

Specimen suitability is assessed before nucleic-acid extraction and other preparation.

03

Measurement and analysis

Testing is performed under the designated workflow and quality indicators are reviewed.

04

Interpretation and reporting

Analytical results are reviewed and reported to the requesting medical institution.

05

Records and support

Process records are retained to support traceability, review and inquiries.

OPERATIONAL PRINCIPLES

Operations designed for reliability

Checks and records at each stage

  • Matching request data with specimen identity
  • Recording receipt condition and preparation steps
  • Reviewing quality indicators during measurement and analysis
  • Checking report content before return to the requester
  • Maintaining records that support review and inquiries

Information coordination with medical institutions

  • Confirming requests and specimen requirements in advance
  • Clear coordination from receipt through reporting
  • Accessible delivery of reports and testing information
  • Ongoing support for review and additional inquiries
  • Development of the domestic testing platform in Fukuoka