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Background: The ability to differentiate between viable and dead microorganisms in metagenomic data is crucial for various microbial inferences, ranging from assessing ecosystem functions of environmental microbiomes to inferring the virulence of potential pathogens from metagenomic analysis. Established viability-resolved genomic approaches are labor-intensive as well as biased and lacking in sensitivity.
Results: We here introduce a new fully computational framework that leverages nanopore sequencing technology to assess microbial viability directly from freely available nanopore signal data. Our approach utilizes deep neural networks to learn features from such raw nanopore signal data that can distinguish DNA from viable and dead microorganisms in a controlled experimental setting of UV-induced Escherichia cell death. The application of explainable artificial intelligence (AI) tools then allows us to pinpoint the signal patterns in the nanopore raw data that allow the model to make viability predictions at high accuracy. Using the model predictions as well as explainable AI, we show that our framework can be leveraged in a real-world application to estimate the viability of obligate intracellular Chlamydia, where traditional culture-based methods suffer from inherently high false-negative rates. This application shows that our viability model captures predictive patterns in the nanopore signal that can be utilized to predict viability across taxonomic boundaries. We finally show the limits of our model's generalizability through antibiotic exposure of a simple mock microbial community, where a new model specific to the killing method had to be trained to obtain accurate viability predictions.
Conclusions: While the potential of our computational framework's generalizability and applicability to metagenomic studies needs to be assessed in more detail, we here demonstrate for the first time the analysis of freely available nanopore signal data to infer the viability of microorganisms, with many potential applications in environmental, veterinary, and clinical settings.
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http://dx.doi.org/10.1093/gigascience/giaf100 | DOI Listing |
An exciting feature of nanopore sequencing is its ability to record multi-omic information on the same sequenced DNA molecule. Well-trained models allow the detection of nucleotide-specific molecular signatures through changes in ionic current as DNA molecules translocate through the nanopore. Thus, naturally occurring DNA modifications, such as DNA methylation and hydroxymethylation, may be recorded simultaneously with the genetic sequence.
View Article and Find Full Text PDFGigascience
January 2025
Helmholtz AI, Helmholtz Zentrum Muenchen, 85764 Neuherberg, Germany.
Background: The ability to differentiate between viable and dead microorganisms in metagenomic data is crucial for various microbial inferences, ranging from assessing ecosystem functions of environmental microbiomes to inferring the virulence of potential pathogens from metagenomic analysis. Established viability-resolved genomic approaches are labor-intensive as well as biased and lacking in sensitivity.
Results: We here introduce a new fully computational framework that leverages nanopore sequencing technology to assess microbial viability directly from freely available nanopore signal data.
ACS Sens
September 2025
Advanced Photonics Center, School of Electronic Science and Engineering, Southeast University Nanjing 210096, China.
Extracellular vesicles (EVs) have emerged as promising biomarkers in cancer diagnostics. However, rapid and nondestructive isolation of EVs from plasma remains challenging due to the presence of abundant interferents with smaller sizes (e.g.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Jiangsu Key Laboratory for Design and Manufacture of Precision Medicine Equipment, School of Mechanical Engineering, Southeast University, Nanjing 211189, China.
Nanofluidic memristors have become a hotspot in neuromorphic computing research due to their potential in modeling biological synaptic functions. However, many existing nanofluidic memristors rely on electrochemical or electric field-driven mechanisms, failing to directly mimic the properties of mechanically gated ion channels (e.g.
View Article and Find Full Text PDFBiosens Bioelectron
August 2025
University of Science and Technology of China, Hefei, 230026, China; Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China; Tianjin Guoke Medical Technology Development Co., Ltd, Tianjin, 300399, China. Electronic address:
In conventional electrochemical biosensors, nanobubbles generated by electrochemical reactions typically adhere to the electrode interface, which affect the accuracy of measurements. In this study, we take good use of nanobubbles as the signal source and effectively address this limitation. An ultrasensitive approach for the detection of miRNA is further developed coupling catalytic hairpin assembly and DNA-functionalized nanopores to generate nanobubbles.
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