TechnologiesDNA-SeqCirculating Tumor DNA

High-sensitivity cfDNA and ctDNA analysis services

Cell-free DNA (cfDNA) and circulating tumor DNA (ctDNA) extraction and analysis services for drug development, from discovery to large clinical trials.

cfDNA and ctDNA analysis in liquid biopsies

Circulating tumor DNA (ctDNA) testing is challenging due to its very low quantities in liquid biopsies and the presence of short, fragmented DNA. This requires an optimized extraction protocol and highly sensitive and robust methodologies, such as next-generation sequencing (NGS), for accurate detection and quantification.

We perform qPCR and dPCR on short cfDNA and ctDNA targets

ctDNA and cfDNA testing services at TATAA

NGS-based ctDNA and cfDNA analysis enables the detection of tumor-derived DNA fragments in the bloodstream, providing non-invasive insights.

  • Monitor residual cancer cells post-treatment by analyzing ctDNA and cfDNA to detect relapse.
  • Track ctDNA and cfDNA levels to assess the effectiveness of ongoing therapies.
  • Detect genetic changes in tumors during treatment by analyzing ctDNA and cfDNA for adaptive therapies.
  • Identify resistance mutations emerging during therapy using ctDNA and cfDNA for timely interventions.
  • Assess tumor mutations non-invasively with cfDNA and ctDNA liquid biopsies, eliminating the need for tissue biopsies.
  • Track ctDNA and cfDNA dynamics to monitor patient responses and disease progression in clinical trials.

Detect and quantify cell free DNA and circulating DNA fragments shed by tumors.

Whole genome sequencing Whole exome sequencing Targeted Gene Panels Circulating Tumor DNA (ctDNA)
Library preparation IDT xGen DNA Library Prep Kit EZ with UDIs IDT xGen DNA Library Prep Kit EZ with UDIs, combined with xGen Exome Hyb Panel v2
Recommended sample input Fresh frozen cells or tissue
EDTA whole blood or PAXgene DNA tubes
High quality FFPE (IDT DNA Integrity score > 1.0)
Fresh frozen cells or tissue
EDTA whole blood or PAXgene DNA tubes
High quality FFPE (IDT DNA Integrity score > 1.0)
Recommended DNA input Range: 0.1 ng – 1 ug
Standard input: 100ng
Range: 0.1 ng – 1 ug
Standard input: 100ng
Range: 0.1 ng – 1 ug
Standard input: 100ng
Range: 0.1 ng – 1 ug
Standard input: 100ng
Recommended sequencing Paired-end sequencing Paired-end sequencing Paired-end sequencing Paired-end sequencing
Deliverables Quality-controlled data
Fastq files
Study report
Quality-controlled data
Fastq files
Study report
Quality-controlled data
Fastq files
Study report
Quality-controlled data
Fastq files
Study report

GLP and GCLP compliant laboratory

We are accredited for Good Laboratory Practice (GLP) by the Swedish Board for Accreditation and Conformity Assessment (SWEDAC) for qPCR, dPCR, and molecular biology. In addition, we are Good Clinical Laboratory Practice (GCLP) compliant to ensure the safe and reliable analysis of clinical samples.

Difference between cfDNA and ctDNA

Cell-free DNA (cfDNA) is fragmented DNA that freely circulates in blood and other biofluids. It can originate from various sources, including fetal DNA in prenatal screenings, donor DNA in transplant rejection monitoring, and immune cell DNA in inflammatory diseases. Circulating tumor DNA (ctDNA) is a subset of cfDNA derived explicitly from tumor cells through apoptosis, necrosis, or active secretion.

Both cfDNA and ctDNA serve as valuable biomarkers in precision medicine, oncology, and disease monitoring. Non-invasive, liquid biopsies assess disease status, treatment response, and progression.

Resources

Overview of bioanalysis in advanced therapies

  • Assay design and validation
  • Regulatory guidelines (EMA and FDA)
  • Challenges and best practices

Genomic biomarker analysis (DNA, RNA, miRNA, ctDNA etc,)

  • Technology overview
  • Analytical validation
  • Regulatory overview

Capability PDF

Download our latest brochure for a summary of our molecular CRO services and capabilities.

Your trusted partner for cfDNA and ctDNA sequencing.