Services – ACGT

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Services

Over 30 years of experience in DNA sequencing and molecular biology.

ACGT offers a comprehensive suite of DNA sequencing services from Sanger to the most up-to-date NGS technologies. Trust in our expertise, our culture of quality and our commitment to the life science research community.

Service Options

Whole Plasmid Sequencing

Long-read sequencing of the complete plasmid or amplicon in a single run using Oxford Nanopore (ONT) technology. Rapid and reliable, no primers needed.

Sanger Sequencing

Our most cost-effective, reliable, and fastest solution for sequencing targeted regions of the genome. Sanger sequencing is also the preferred method for validating Next Generation Sequencing (NGS) studies.

Next Generation Sequencing

ACGT offers a comprehensive suite of NGS solutions, from standard to custom services, including extraction, flexible library prep options, short-read and long-read sequencing and robust bioinformatics capabilities.

SNP Genotyping

Providing insights into genetic diversity, inheritance, and evolution, SNP genotyping is a versatile tool in genetics and genomics research; a genetic analytic method used to identify single nucleotide variations in a target genome.

Copy Number Variation

CNVs are genomic alterations that result in abnormal copies of one or more genes, which can be caused by structural genomic events such as duplications, deletions, translocations and inversions.

Fragment Length Analysis

DNA Fragment Length Analysis (FLA) is a versatile tool with numerous applications in both research and clinical settings, contributing to advancements in genetics, diagnostics, and personalized medicine.

Bioinformatics

Comprehensive bioinformatics services and end-to-end solutions to help you interpret it. Our bioinformatics professionals take pride in data accuracy, reliable output, fast turnaround, and thorough customer support.