Variant Analysis

Accurate identification and comprehensive interpretation of genetic variants.

ACGT utilizes a suite of powerful sequence analysis tools to investigate virtually any type of DNA alteration, including single nucleotide variants (SNVs), insertions and deletions (InDels), copy number changes (CNVs), and chromosomal aberrations. With the unprecedented scale of datasets, variants are interpreted through aggregation of public databases and custom curation for their incidence, zygosity, consequence, and/or genotyping.

Sequence data is aligned to reference and analyzed for variants (SNPs, InDels, CNVs). Detected variants are visualized and interpreted for their consequence.

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.

Request a custom project proposal for any application

Upon receipt of your quote request you can expect a timely response with questions about your intended study. ACGT will then provide you with a study proposal detailing the methods, materials and equipment used to execute your study, along with a timetable, expected costs and deliverables.