Evidence map›Paper›PMID 42285091›Full record

ArticleCell reports. Medicine2026

Toward generalizable prediction of cancer signal using a cell-free DNA language model.

Yang Xu, Hua Bao, Daxin Huang, Kun Zhang, Junfei Zhu, Liu Yang, Shengling Fu, Zhili Chang, Jinfeng Zhang, Shuang Chang and 5 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Yang XuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Hua BaoGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Daxin HuangDepartment of Radiation Oncology, Fujian Medical University Union Hospital, Fuzhou, China.
Kun ZhangDepartment of Thoracic Surgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Junfei ZhuDepartment of Respiratory and Critical Care Medicine, Taizhou Central Hospital, Taizhou, China.
Liu YangColorectal Center, Jiangsu Cancer Hospital, Nanjing, China.
Shengling FuDepartment of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Zhili ChangGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Jinfeng ZhangGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Shuang ChangGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Baihan ZhuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Shuyu WuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Shanshan YangGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Xue WuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Yang ShaoGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China; School of Public Health, Nanjing Medical University, Nanjing, China. Electronic address: yang.shao@geneseeq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-free DNA can be used for early cancer detection, minimal residual disease monitoring, and post-treatment risk stratification. However, current assays are often designed for a single purpose and rely on deep or broad sequencing panels that capture only a small fraction of tumor-derived signals, limiting transferability, increasing cost, and reducing scalability. Fragmentia-AI is an artificial intelligence language model that learns fragment-level sequence patterns in tumor-derived cell-free DNA. Instead of focusing on mutations, it uses the structure of cell-free DNA to detect cancer signals in a partially panel-agnostic manner from ultra-low sequencing input, approximately 0.1%-1% of conventional depth. The model performs well across cancer types and clinical settings, including monitoring after surgery or immunotherapy, and in samples with low variant allele frequencies or no detected mutations. Fragment-level analyses identify shorter fragments and tumor-derived sequence patterns across panels of different sizes and ultra-low-pass whole-genome sequencing in multiple cohorts.

Indexed as

Cell-Free Nucleic AcidsNeoplasmsArtificial IntelligenceHigh-Throughput Nucleotide SequencingHumansMutationCell-Free Nucleic Acidsartificial intellegencecell free DNAearly cancer detectionfragmentomicslarge language modelminimal residual diseaseultra-low sequencingwhole genome sequencing

Identifiers

PMID42285091
PMCPMC13400139

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.