8th Annual Congress of Liquid Biopsy (ISLB 2026)

7 November 2026
to 9 November 2026
The Meliá Castilla Hotel & Convention Center
, Madrid
, Spain

Visit biomodal at booth 

About the event

Join biomodal at ISLB 2026, the only global congress dedicated exclusively to liquid biopsy, in Madrid from 7-9 November 2026.

biomodal is proud to contribute to the conference program with three poster presentations, showcasing how our 6-base sequencing technology is advancing ultrasensitive detection, fragmentomics, and biomarker discovery in liquid biopsy research.

Come visit our posters to learn more about biomodal’s duet technology and see how our solutions are helping researchers uncover a more complete picture of disease biology.

Introducing duet mosaic™
biomodal is excited to introduce the newly launched duet mosaic™ family, new workflows designed for cfDNA and liquid biopsy research that combine genetic, epigenetic, and fragmentomic information from the same molecules, including short, damaged fragments other workflows may miss. When your sample is limited, every fragment matters, and duet mosaic helps researchers access more from every molecule.

Want to connect one-on-one? Complete the form below to schedule a meeting with the biomodal team before, during, or after the show.

Presenting at the event

(226) Integrated 6-base cfDNA Profiling Reveals Complementary Genetic, Epigenetic and Fragmentomic Biomarkers, Enabling Optimal Biomarker Combinations for Cancer Detection

Robert Blanshard

Product Manager

biomodal

Poster #: PP.35

Cell-free DNA (cfDNA) contains multiple layers of biological information, including epigenetic modifications, genetic alterations and fragmentation patterns that are informative for cancer detection. However, these features are typically profiled using separate assays, increasing sample requirements and analytical complexity. We evaluated 6-base sequencing’s ability to simultaneously capture complementary cfDNA signals from a single sample and support multimodal biomarker discovery in colorectal cancer (CRC).

Using duet evoC, we sequenced 10 ng cfDNA from healthy individuals and patients with Stage I-IV CRC. The assay simultaneously identifies the four canonical bases, distinguishes 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) and preserves native fragmentomic information. This enabled concurrent extraction of epigenetic features derived from 5mC and 5hmC profiles, genetic features including sequence variation and mutational signatures, and fragmentomic features including fragment length distributions, nucleosome occupancy patterns and 6-base end motifs.

Independent machine-learning classifiers trained on epigenetic, genetic or fragmentomic features discriminated CRC from healthy, demonstrating that all modalities capture disease-associated information. However, the relative contribution of biomarker classes varied across disease stages and samples, indicating that distinct cfDNA features reflect complementary aspects of tumour biology. Epigenetic, genetic and fragmentomic classifiers showed overlapping but non-identical classification patterns, suggesting substantial orthogonality between modalities. Integration of modality-specific predictions consistently improved performance compared with individual models, highlighting the value of combining multiple cfDNA-derived signals within a unified analytical framework.

These findings demonstrate that simultaneous profiling of methylation, hydroxymethylation, mutations and fragmentation patterns can provide a more comprehensive view of tumour-associated biology than any single modality alone. By preserving multiple complementary biomarker classes within a single workflow, 6-base sequencing enables adaptive multimodal liquid biopsy strategies that accommodate biological heterogeneity across patients and disease stages. This integrated approach provides a foundation for next-generation biomarker models that leverage the most informative cfDNA signals, supporting more precise strategies for cancer detection and monitoring.

(227) Fragment-level Integration of Epigenetic and Genetic Signals for Ultra-sensitive ctDNA Detection in Liquid Biopsy and MRD Applications

Robert Blanshard

Product Manager

biomodal

Poster #: PP.36

Sensitive detection of circulating tumour DNA (ctDNA) is critical for liquid biopsy applications including early cancer detection and minimal residual disease (MRD) monitoring, where disease-associated molecules may be present at very low abundance. Genetic and epigenetic alterations represent complementary sources of information within cfDNA, yet are typically evaluated independently. The 6-base genome, provided by duet evoC, provides the canonical 4-base genome whilst simultaneously distinguishing 5-methylcytosine (5mC) from 5-hydroxymethylcytosine (5hmC) to provide the 5th and 6th, epigenetic bases. The 6-base genome has been shown to be a powerful tool for the discovery of biomarkers of early biological change and provides mechanistic insight across important applications including oncology, liquid biopsy and neurology.

Here we present the next evolution of the duet product portfolio. Through a novel single-stranded ligation approach, we demonstrate markedly improved material recovery and methylation calling sensitivity, whilst maintaining high genetic and epigenetic accuracy. Single-stranded ligation preserves original cfDNA strands, whereas traditional end-repair fills in 5′ overhangs with unmodified cytosines, reducing sensitivity, and degrades 3′ overhangs, lowering information content. Benchmarking against alternative sequencing workflows confirmed improved methylation calling performance, accurate genetic variant calling performance, including C>T variants at CpG sites, and accurate determination of fragmentomic features.

Using contrived samples containing methylated and unmethylated samples of genetically distinct backgrounds, we assessed analytical limit of detection from genetic features, epigenetic features, and both combined. Combining accurate methylation and genetic calls enabled detection in the low parts-per-million range. By simultaneously capturing genetic variation, 5mC and 5hmC, 6-base sequencing provides multiple independent layers of evidence from a single cfDNA sample, offering a clinically relevant framework for ctDNA detection in MRD monitoring and early cancer detection.

(244) Removal of End-repair Reduces Hypomethylation Artefacts and Improves ctDNA Detection and Tissue-of-origin Determination in cfDNA Assays

Robert Blanshard

Product Manager

biomodal

Poster #: PP.37

End-repair and A-tailing (ERAT) is a popular method in the preparation of DNA fragments for sequencing in methylation assays.

However, the end repair step introduces bases that were not originally present within the source material. This is particularly relevant when unmodified cytosines are added in the place of cytosines that were methylated or hydroxymethylated in the original DNA. Furthermore, the polymerases used in end repair can act from nicks internal to a DNA molecule and so can replace large portions of it with non-original nucleotides. This artificially suppresses the apparent levels of methylation that are detected in the assay and, in the most extreme cases, lead to fragments appearing to be artefactually heavily (or entirely) hypomethylated.

Analysis of methylation in cfDNA relies upon the accurate determination of the modification status of each cytosine at the level of individual DNA fragments. Hypomethylation artefacts can dramatically impede the utility of these assays in cases such as MRD detection in liquid biopsies where tumor-derived fragments are present at very low levels.

The duet cfDNA assays (both 5 base and 6 base) ligate sequencing adaptors directly to single-stranded molecules without an end-repair step. Here, we show that this removes the apparent hypomethylation artefact that is present in other assays that rely upon end repair followed by enzymatic conversion for methylation analysis.

The elimination of hypomethylation artifacts improves methylation limit of detection and therefore improves the ability of the assay to detect ctDNA when compared to approaches that use end repair and A-tailing. This distinction improves the power of the technology to discover the most performative liquid biopsy biomarkers using 5mC, 5hmC, complete genetics, including C>T variants, and fragmentomic information.

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Attending from biomodal

Robert Blanshard

Robert Blanshard, PhD

Product Manager

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ISLB 2026 7-9NOV26

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