Evidence map›Paper›PMID 42102803›Full record

ArticleCell reports methods2026

A multiplex PCR-based sequencing method for the diagnosis and differentiation of echinococcosis using plasma samples, a proof-of-concept study.

Yanping Zhao, Yeqin Wang, Ming Zhi, Lin Yang, Wending Pang, Tian Chen, Yiyang Shi, Shu Shen, Hong-Bin Yan, Chunyang Li and 4 more

Abstract read
In one paragraph

Article in Cell reports methods, 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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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

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

14 authors.

Yanping ZhaoBGI Research, Shenzhen 518083, China; BGI Research, Chongqing 401329, China.
Yeqin WangBGI Research, Shenzhen 518083, China.
Ming ZhiDepartment of Hepatobiliary Surgery II, The People's Hospital of Ganzi Tibetan Autonomous Prefecture, Kangding, Sichuan 626000, China.
Lin YangBGI Research, Shenzhen 518083, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Wending PangBGI Research, Shenzhen 518083, China; BGI Research, Chongqing 401329, China; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China.
Tian ChenBGI Research, Shenzhen 518083, China.
Yiyang ShiDepartment of Hepatobiliary Surgery II, The People's Hospital of Ganzi Tibetan Autonomous Prefecture, Kangding, Sichuan 626000, China.
Shu ShenDepartment of Liver Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, China.
Hong-Bin YanState Key Laboratory for Animal Disease Control and Prevention, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.
Chunyang LiBiomedical Big Data Center, Med-X Center for Informatics, West China Hospital of Sichuan University, Chengdu, China. Electronic address: lichunyang@wchscu.cn.
Gengfu WeiDepartment of Hepatobiliary Surgery II, The People's Hospital of Ganzi Tibetan Autonomous Prefecture, Kangding, Sichuan 626000, China. Electronic address: 18030916298@163.com.
Yanyan ZhangBGI Research, Shenzhen 518083, China. Electronic address: zhangyanyan@genomics.cn.
Xin JinState Key Laboratory of Genome and Multi-Omics Technologies, BGI Research, Shenzhen, China; Shenzhen Key Laboratory of Transomics Biotechnologies, Shenzhen, China; Shanxi Medical University-BGI Collaborative Center for Future Medicine, Shanxi Medical University, Taiyuan, China. Electronic address: jinxin@genomics.cn.
Yan ZhangState Key Laboratory of Genome and Multi-Omics Technologies, BGI Research, Shenzhen, China; Shenzhen Key Laboratory of Transomics Biotechnologies, Shenzhen, China. Electronic address: zhangyan15@genomics.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Echinococcosis poses a significant public health threat, and its diagnosis relies on imaging. Non-invasive plasma detection of Echinococcus cell-free DNA (cfDNA) offers a promising diagnostic approach. We developed a low-cost multiplex PCR panel with 230 primer pairs targeting Echinococcus mitochondrial genomes and nuclear DNA repeat regions. We validated the panel using gradient dilutions of two pathogen species' DNA and 81 plasma samples (53 patients and 28 controls), differentiating species through sequencing analysis. Our method detected Echinococcus genomic DNA at an input as low as 1 fg per reaction, and tests of clinical samples showed a sensitivity of 68.42% and specificity of 92.86%. Based on our detection, 80% of the clinically confirmed cases were correctly identified as positive echinococcosis cases, and cfDNA levels correlated significantly with lesion size. This study highlights the potential of targeted cfDNA sequencing for non-invasive echinococcosis diagnosis and species differentiation and offers a promising tool for doubtful cases.

Indexed as

EchinococcosisEchinococcusMultiplex Polymerase Chain ReactionSequence Analysis, DNAAnimalsCell-Free Nucleic AcidsDNA, HelminthFemaleHumansMaleProof of Concept StudySensitivity and SpecificityCell-Free Nucleic AcidsDNA, Helminthcell-free DNACP: microbiologyCP: molecular biologyechinococcosisEchinococcus granulosusEchinococcus multilocularisliquid biopsynon-invasive diagnosistarget sequencing

Identifiers

PMID42102803
PMCPMC13282652

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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.