Custom Project

End-to-end biology testing solutions, personalized for your research goals.

ACGT provides molecular biology and sequencing solutions, with flexible service levels and competitive pricing, personalized for your research objectives and regulatory submissions. 

With 30 years’ experience in DNA sequencing and molecular biology services, ACGT understands your needs. Trust in our expert staff with the highest quality customer service and research execution.

Service Platform

We incorporate multiple state-of-the-art analytic technologies in designing customized workflows for diverse sample types.

Sanger Sequencing

Next Generation Sequencing

Copy Number Analysis

Fragment Length Analysis

Service Description​

Contact us with your custom project needs, and we will respond within 1-3 business days.

  • Personalized project proposal, designed specific to your project requirements and/or scope of work
  • Status updates (e.g. sample receipt, testing progress, any issues or complications) provided periodically and upon request
  • Consultation with dedicated project manager, ACGT Scientific Director, and bioinformatics analyst via email, phone or e-meetings
  • Project report and deliverables (raw data and all analysis results) upon completion 
  • All testing materials and generated data managed, archived, and purged

Committed to Quality

Our NGS services are offered at the following quality grades, up to cGMP compliance. ACGT pursues a culture of quality with an aim towards continuous improvement. Our rigorous quality management systems (QMS) ensure compliance with Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) sequence analysis in regulatory grade sequencing and molecular biology studies.

Credentials

ACGT’s rigorous Quality Assurance Program ensures strict regulatory compliance and performance standards.

Credentials

ACGT’s rigorous Quality Assurance Program ensures strict regulatory compliance and performance standards.

  • Compliant with Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP)
  • Compliant with HIPAA regulations for clinical work
  • Strictly implemented Standard Operating Procedures (SOP) and Work Instructions (WI)
  • Independent Quality Assurance Unit (QAU) segregated from conducting laboratory studies and procedures
  • Regular internal audits to ensure compliance and target continuous improvement
  • Compliant with US FDA regulations covering GLP Compliance with Biosafety Level 2 (BSL-2) regulations
  • Electronic Record Retention and Archiving in compliance with GLP
  • Regular Training and internal certification of each employee in GLP, HIPPA and safety protocols
  • Vendor, service provider, and equipment qualification programs
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