Singapore scientists created Fragle, an AI model that identifies cancer progression through blood DNA fragment analysis. Unlike traditional methods, it skips expensive sequencing by focusing on size variations in tumor DNA. The tool has shown high accuracy across diverse cancers and integrates with hospital lab workflows. Researchers are now testing its ability to predict treatment outcomes in real-time clinical trials.
June 16, 2025
New AI tool analyses DNA for faster, affordable cancer monitoring
"Just as scientists tracked Covid-19
outbreaks by detecting viral particles in wastewater, Fragle analyses DNA
fragments in blood to monitor cancer treatment response and detect relapse
early" – Dr. Anders Skanderup, A*STAR GIS
A team of researchers from Singapore has
developed a new artificial intelligence (AI)-based method that makes tracking
cancer easier and faster-using blood tests.
Key Points
1 AI tool detects cancer DNA patterns from blood
fragments
2 Reduces reliance on costly mutation sequencing
3 Works across 100+ patients and cancer types
4 Enables bi-monthly relapse monitoring during
therapy
The method called "Fragle",
developed by a team from the A*STAR Genome Institute of Singapore (A*STAR GIS),
requires only a small blood sample, and analyses the size of DNA fragments in
the blood to reveal distinct patterns that differentiate cancer DNA from
healthy DNA. This can help doctors track cancer treatment responses more
accurately and frequently.
"Just as scientists tracked Covid-19
outbreaks by detecting viral particles in wastewater, Fragle analyses DNA
fragments in blood to monitor cancer treatment response and detect relapse
early," said lead author Dr. Anders Skanderup, Senior Principal Scientist
at A*STAR GIS Laboratory of Computational Cancer Genomics.
Existing methods for measuring cancer DNA in
the blood, also known as circulating tumour DNA (ctDNA), often require complex
and expensive DNA sequencing to screen for common cancer mutations. However,
because cancer mutations vary between patients, test results can be
inconsistent, making it difficult for doctors to track cancer treatment
response with blood tests effectively.
On the other hand, Fragle uses AI to analyse
the size of DNA fragments in the blood.
Cancer DNA tends to exhibit different size
patterns compared to healthy DNA, and the Fragle AI-model can identify these
differences using very small amounts of DNA. As a result, the method allows for
faster and more affordable cancer tracking, said the researchers in the paper,
published in the journal Nature Biomedical Engineering.
It has also demonstrated high reliability,
delivering accurate results across blood samples from hundreds of cancer
patients and distinct cancer types. In addition, the method is versatile and
compatible with most DNA profiling techniques commonly used in hospitals or
offered by commercial providers.
In an ongoing study of more than 100 clinical
trial patients, the GIS-NCCS team is using Fragle to monitor ctDNA levels every
two months during treatment, with the aim of catching signs of relapse before
they appear on routine scans.
The team is also studying whether early
changes in ctDNA can identify which patients are likely to have a favourable or
poor response to the therapy. The goal of the study is to assess the value of
incorporating ctDNA tests in routine monitoring of cancer patients during
treatment.
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