Some of the most harmful genetic changes in cancer are also the hardest to see. These structural alterations, deep within a tumor’s DNA, can fuel aggressive growth and evade standard testing, especially when tissue samples are small or degraded.
To address this challenge, Mayo Clinic researchers have developed a new computational tool called BACDAC that shines a light on these elusive genomic patterns. The tool helps researchers identify signs of genomic instability using DNA sequencing that reads the entire genome, even in low-purity or low-coverage samples.
The tool could help clinicians better predict how a tumor will behave and guide more personalized treatment choices.
Detecting chromosome changes
At the core of BACDAC’s approach is the concept of ploidy, which refers to the number of complete sets of chromosomes in a cell. While normal human cells have two sets (46 chromosomes total), cancer cells often show large-scale gains or losses, disrupting this balance and enabling unchecked growth.
In a study published in Genome Biology, the research team used BACDAC to analyze more than 650 tumors across 12 cancer types. The tool helped researchers detect signs of whole-genome doubling, where a tumor duplicates all of its DNA. This type of abnormal ploidy is often linked to aggressive behavior and treatment resistance.
“This tool lets us see a layer of the genome that’s been invisible until now,” says George Vasmatzis, Ph.D., a lead author of the study and co-director of Mayo Clinic’s Biomarker Discovery Program. “We’ve spent decades studying the biology of genomic instability. This is the first time we’ve been able to translate that knowledge into a tool that works at scale.”
BACDAC also provides a visual summary of a tumor’s genomic landscape. A custom output called the Constellation Plot offers an intuitive view of whether the tumor’s chromosomes are stable or disrupted. This may help researchers and pathologists interpret results more easily.
Next, the Mayo Clinic team plans to further validate BACDAC and develop it into a clinically deployable diagnostic tool. It may help inform treatment decisions by providing a clearer view of a tumor’s structural changes.
More information:
Sarah H. Johnson et al, Tumor ploidy determination in low-pass whole genome sequencing and allelic copy number visualization using the Constellation Plot, Genome Biology (2025). DOI: 10.1186/s13059-025-03599-2
2025 Tribune Content Agency, LLC.
Citation:
Computational tool exposes hidden cancer DNA changes that may drive treatment resistance (2025, June 21)
retrieved 21 June 2025
from https://medicalxpress.com/news/2025-06-tool-exposes-hidden-cancer-dna.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.
Some of the most harmful genetic changes in cancer are also the hardest to see. These structural alterations, deep within a tumor’s DNA, can fuel aggressive growth and evade standard testing, especially when tissue samples are small or degraded.
To address this challenge, Mayo Clinic researchers have developed a new computational tool called BACDAC that shines a light on these elusive genomic patterns. The tool helps researchers identify signs of genomic instability using DNA sequencing that reads the entire genome, even in low-purity or low-coverage samples.
The tool could help clinicians better predict how a tumor will behave and guide more personalized treatment choices.
Detecting chromosome changes
At the core of BACDAC’s approach is the concept of ploidy, which refers to the number of complete sets of chromosomes in a cell. While normal human cells have two sets (46 chromosomes total), cancer cells often show large-scale gains or losses, disrupting this balance and enabling unchecked growth.
In a study published in Genome Biology, the research team used BACDAC to analyze more than 650 tumors across 12 cancer types. The tool helped researchers detect signs of whole-genome doubling, where a tumor duplicates all of its DNA. This type of abnormal ploidy is often linked to aggressive behavior and treatment resistance.
“This tool lets us see a layer of the genome that’s been invisible until now,” says George Vasmatzis, Ph.D., a lead author of the study and co-director of Mayo Clinic’s Biomarker Discovery Program. “We’ve spent decades studying the biology of genomic instability. This is the first time we’ve been able to translate that knowledge into a tool that works at scale.”
BACDAC also provides a visual summary of a tumor’s genomic landscape. A custom output called the Constellation Plot offers an intuitive view of whether the tumor’s chromosomes are stable or disrupted. This may help researchers and pathologists interpret results more easily.
Next, the Mayo Clinic team plans to further validate BACDAC and develop it into a clinically deployable diagnostic tool. It may help inform treatment decisions by providing a clearer view of a tumor’s structural changes.
More information:
Sarah H. Johnson et al, Tumor ploidy determination in low-pass whole genome sequencing and allelic copy number visualization using the Constellation Plot, Genome Biology (2025). DOI: 10.1186/s13059-025-03599-2
2025 Tribune Content Agency, LLC.
Citation:
Computational tool exposes hidden cancer DNA changes that may drive treatment resistance (2025, June 21)
retrieved 21 June 2025
from https://medicalxpress.com/news/2025-06-tool-exposes-hidden-cancer-dna.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.
