Evidence map›Paper›PMID 42414258›Full record

ArticleMicrosystems & nanoengineering2026

A fully integrated and automated 24-sample microfluidic system for sample-in-amplicon-out forensic analysis.

Jun Nie, Yong Fan, Jichen Li, Jiaming Peng, Fuchun Li, Xiaoyue Luo, Lihuan Huang, Xiaochun Wan, Dehong Yan, Wenting Bu and 2 more

Abstract read
In one paragraph

Article in Microsystems & nanoengineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Jun Nie *Guangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Yong Fan *Guangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Jichen LiGuangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Jiaming PengCollege of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Fuchun LiGuangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Xiaoyue LuoGuangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Lihuan HuangShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Xiaochun WanShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Dehong YanShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Wenting BuGuangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. wt.bu@siat.ac.cn.
Song XuShenzhen Qixu Technology Co., Ltd, Shenzhen, China. xusong@daphina.net.
Yongfan MenGuangdong Provincial Key Laboratory of Biomedical Optical Imaging Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. yf.men@siat.ac.cn.ORCID http://orcid.org/0000-0001-8265-1787

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32500620Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2023A1515110971Shenzhen Science and Technology Innovation Commission JCYJ20220531100803007
6 · The paper itself

Abstract

Rapid, reliable, and high-throughput DNA profiling is critical to modern forensic science. However, current analytical platforms are often limited by low sample throughput, insufficient system integration, and high operational costs. Here we report a fully integrated microfluidic system capable of performing automated, end-to-end forensic DNA analysis of 24 samples in parallel, with a coefficient of variation (CV) of merely 3.14%. The system incorporates sequential modules for cell lysis, magnetic bead-based DNA extraction and purification, multiplex PCR amplification, and product export for STR analysis within a sealed cartridge. Fluidic connectivity among four functional regions is precisely controlled via electromagnetic membrane valves, while automated reagent handling is achieved through solenoid and rotary valve systems. The platform yields high-quality STR amplicons from both buccal swabs and FTA cards, demonstrating complete concordance with conventional laboratory methods. Total 24-sample processing time is under 6 h, with a per-sample cost below $50. This technology offers a potential solution for high-throughput forensic DNA analysis.

Identifiers

PMID42414258
PMCPMC13341781

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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.