Evidence map›Paper›PMID 42847779›Full record

ArticleBriefings in bioinformatics2026

Deconformer: efficient cell-type composition profiling of cfRNA across diverse cell types.

Chaoxing Wang, Xuetao Tian, Shuo Yan, Jinghua Sun, Sujun Zhu, Jiayi Li, Chu Shi, Tingyu Yang, Yulong Qin, Zhongzhen Liu and 7 more

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

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0citing papers in PubMed
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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Chaoxing WangCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Xuetao TianFaculty of Psychology, Beijing Normal University, Xinjiekouwai Street, Haidian District, Beijing 100875, Beijing, China.
Shuo YanCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Jinghua SunState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.
Sujun ZhuObstetrics Department, Shenzhen Maternity and Child Healthcare Hospital, Hongli Road, Futian District, Shenzhen 518028, Guangdong, China.
Jiayi LiCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Chu ShiState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.
Tingyu YangCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Yulong QinCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Zhongzhen LiuState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.
Juan ZengObstetrics Department, Shenzhen Maternity and Child Healthcare Hospital, Hongli Road, Futian District, Shenzhen 518028, Guangdong, China.
Dongyue YuCollege of Life Sciences, Nankai University, Weijin Road, Nankai District, Tianjin 300071, Tianjin, China.
Wentao LiuCollege of Life Sciences, University of Chinese Academy of Sciences, Yuquan Road, Shijingshan District, Beijing 100049, Beijing, China.
Chengbin HuState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.
Qing ZhouState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.
Xin JinState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.ORCID 0000-0001-7554-4975
Wen-Jing WangState Key Laboratory of Genome and Multi-omics Technologies, BGI Research, Yunhua Road, Yantian District, Shenzhen 518083, Guangdong, China.ORCID 0000-0002-4527-1168

Funding

National Natural Science Foundation of China grant 62207002National Natural Science Foundation of China grant U23A20402Science, Technology and Innovation Commission of Shenzhen Municipality grant JCYJ20170412152854656
6 · The paper itself

Abstract

Resolving cell-type contributions in cell-free RNA (cfRNA) profiles is important for liquid-biopsy research, but profiling many potential cellular sources remains computationally challenging. Here, we present Deconformer, a biologically informed deep-learning framework that integrates pathway knowledge into a Transformer architecture to estimate relative cfRNA contributions across 60 major human cell types. In systematic benchmarks using cross-platform simulations selected for similarity to real plasma cfRNA, Deconformer showed improved robustness from pathway-informed modeling and achieved competitive accuracy with substantially lower computational cost than established deconvolution methods. Applied to real cfRNA cohorts, it recapitulated known gestational trajectories and detected disease-associated composition shifts, supporting its use as a practical framework for large-scale cfRNA profiling.

Indexed as

Cell-Free Nucleic AcidsDeep LearningSoftwareHumansLiquid BiopsyCell-Free Nucleic Acidscell-free RNAcell-type compositiondeep learningliquid biopsy

Identifiers

PMID42847779

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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.