Evidence map›Paper›PMID 35684650›Full record

ArticleSensors (Basel, Switzerland)2022

A Source Localization Method Using Complex Variational Mode Decomposition.

Qiuyan Miao, Xinglin Sun, Bin Wu, Lingyun Ye, Kaichen Song

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2022. 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

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

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

5 authors.

Qiuyan MiaoCollege of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.ORCID 0000-0002-2725-0857
Xinglin SunCollege of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.ORCID 0000-0002-0019-850X
Bin WuCollege of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.ORCID 0000-0001-9401-219X
Lingyun YeCollege of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.
Kaichen SongCollege of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Source localization with a passive sensors array is a common topic in various areas. Among the popular source localization algorithms, the compressive sensing (CS)-based method has recently drawn considerable interest because it is a high-resolution method, robust with coherent sources and few snapshots, and applicable for mixed near-field and far-field source localization. However, the CS-based methods rely on the dense grid to ensure the required estimation precision, which is time-consuming and impractical. This paper applies the complex variational mode decomposition (CVMD) to source localization. Specifically, the signal model of the source localization problem is similar to the time-domain frequency-modulated signal model. Motivated by this, we extend CVMD, initially designed for nonstationary time-domain signal analysis, to array signal processing. The decomposition results of the array measurements can correspond to the potential sources at different locations. Then, the sources' direction and range can be estimated by model fitting with the decomposed subsignals. The simulation results show that the proposed CVMD-based method can locate the pure far-field, pure near-field, mixed far-field, and near-field sources. Notably, it can yield high-resolution localization for the coherent sources with one single snapshot with low computing time.

Indexed as

complex variational mode decompositioncompressive sensingfar-field sourcenear-field sourcesource localization

Identifiers

PMID35684650
PMCPMC9185352

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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.