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NiReject:用于功能近红外光谱中自动坏通道检测

NiReject: toward automated bad channel detection in functional near-infrared spectroscopy.

作者信息

Gerloff Christian, Yücel Meryem A, Mehlem Lena, Konrad Kerstin, Reindl Vanessa

机构信息

JARA Brain Institute II, Molecular Neuroscience and Neuroimaging (INM-11), Jülich Research Centre, Jülich, Germany.

University Hospital RWTH Aachen, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Child Neuropsychology Section, Aachen, Germany.

出版信息

Neurophotonics. 2024 Oct;11(4):045008. doi: 10.1117/1.NPh.11.4.045008. Epub 2024 Nov 4.

DOI:10.1117/1.NPh.11.4.045008
PMID:39497725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11532795/
Abstract

SIGNIFICANCE

The increasing sample sizes and channel densities in functional near-infrared spectroscopy (fNIRS) necessitate precise and scalable identification of signals that do not permit reliable analysis to exclude them. Despite the relevance of detecting these "bad channels," little is known about the behavior of fNIRS detection methods, and the potential of unsupervised and semi-supervised machine learning remains unexplored.

AIM

We developed three novel machine learning-based detectors, unsupervised, semi-supervised, and hybrid NiReject, and compared them with existing approaches.

APPROACH

We conducted a systematic literature search and demonstrated the influence of bad channel detection. Based on 29,924 signals from two independently rated datasets and a simulated scenario space of diverse phenomena, we evaluated the NiReject models, six of the most established detection methods in fNIRS, and 11 prominent methods from other domains.

RESULTS

Although the results indicated that a lack of proper detection can strongly bias findings, detection methods were reported in only 32% of the included studies. Semi-supervised models, specifically semi-supervised NiReject, outperformed both established thresholding-based and unsupervised detectors. Hybrid NiReject, utilizing a human feedback loop, addressed the practical challenges of semi-supervised methods while maintaining precise detection and low rating effort.

CONCLUSIONS

This work contributes toward more automated and reliable fNIRS signal quality control by comprehensively evaluating existing and introducing novel machine learning-based techniques and outlining practical considerations for bad channel detection.

摘要

意义

功能近红外光谱(fNIRS)中样本量和通道密度不断增加,这就需要精确且可扩展地识别那些不允许进行可靠分析从而需排除的信号。尽管检测这些“坏通道”很重要,但对于fNIRS检测方法的行为知之甚少,并且无监督和半监督机器学习的潜力仍未得到探索。

目的

我们开发了三种基于机器学习的新型检测器,即无监督、半监督和混合式NiReject,并将它们与现有方法进行比较。

方法

我们进行了系统的文献检索,并展示了坏通道检测的影响。基于来自两个独立评级数据集的29924个信号以及各种现象的模拟场景空间,我们评估了NiReject模型、fNIRS中六种最成熟的检测方法以及其他领域的11种突出方法。

结果

尽管结果表明缺乏适当的检测会严重影响研究结果,但在所纳入的研究中,仅32%报告了检测方法。半监督模型,特别是半监督NiReject,优于既定的基于阈值的检测器和无监督检测器。混合式NiReject利用人工反馈回路,在保持精确检测和低评级工作量的同时,解决了半监督方法的实际挑战。

结论

这项工作通过全面评估现有方法并引入基于机器学习的新技术,以及概述坏通道检测的实际考虑因素,为实现更自动化和可靠的fNIRS信号质量控制做出了贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/c12a512720c9/NPh-011-045008-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/ba603c28db0a/NPh-011-045008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/b61c47c4b051/NPh-011-045008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/8c78cfc671b7/NPh-011-045008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/a8bca3f0a2f9/NPh-011-045008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/eb77c2d3c5df/NPh-011-045008-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/a4d290f32f4b/NPh-011-045008-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/66482e07f1ff/NPh-011-045008-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/9ca5848549e2/NPh-011-045008-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/c12a512720c9/NPh-011-045008-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/ba603c28db0a/NPh-011-045008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/b61c47c4b051/NPh-011-045008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/8c78cfc671b7/NPh-011-045008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/a8bca3f0a2f9/NPh-011-045008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/eb77c2d3c5df/NPh-011-045008-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/a4d290f32f4b/NPh-011-045008-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/66482e07f1ff/NPh-011-045008-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/9ca5848549e2/NPh-011-045008-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e24/11532795/c12a512720c9/NPh-011-045008-g009.jpg

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