ArticleSensors (Basel, Switzerland)2021
WiFi Fingerprinting Indoor Localization Based on Dynamic Mode Decomposition Feature Selection with Hidden Markov Model.
Article in Sensors (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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.
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.
Who cites it
6 citing papers in PubMed.
- Comprehensive analysis of security threats and privacy issues in indoor localization systems.Scientific reports · 2025Article
- An Indoor Fingerprint Positioning Algorithm Based on WKNN and Improved XGBoost.Sensors (Basel, Switzerland) · 2023Article
- Precision Enhancement of Wireless Localization System Using Passive DOA Multiple Sensor Network for Moving Target.Sensors (Basel, Switzerland) · 2022Article
- MineBL: A Battery-Free Localization Scheme with Binocular Camera for Coal Mine.Sensors (Basel, Switzerland) · 2022Article
- A Novel Valued Tolerance Rough Set and Decision Rules Method for Indoor Positioning Using WiFi Fingerprinting.Sensors (Basel, Switzerland) · 2022Article
- Vertical Handover Prediction Based on Hidden Markov Model in Heterogeneous VLC-WiFi System.Sensors (Basel, Switzerland) · 2022Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Over the years, WiFi received signal strength indicator (RSSI) measurements have been widely implemented for determining the location of a user's position in an indoor environment, where the GPS signal might not be received. This method utilizes a huge RSSI dataset collected from numerous access points (APs). The WiFi RSSI measurements are nonlinear with distance and are largely influenced by interference in the indoor environment. Therefore, machine learning (ML) techniques such as a hidden Markov model (HMM) are generally utilized to efficiently identify a trend of RSSI values, which corresponds to locations around a region of interest. Similar to other ML tools, the performance and computing cost of the HMM are dependent on the feature dimension since a large quantity of RSSI measurements are required for the learning process. Hence, this article introduces a feature extraction method based on dynamic mode decomposition (DMD) for the HMM to effectively model WiFi fingerprint indoor localization. The DMD is adopted since it decomposes RSSIs to meaningful spatial and temporal forms over a given time. Here, the mode forms are analytically reconstructed to produce low-dimensional feature vectors, which are used with the HMM. The localization performance of the proposed HMM-DMD is compared with other well-known ML algorithms for WiFi fingerprinting localization using simulations. The results show that the HMM-DMD algorithm yields a significant localization performance improvement, accuracy, and reasonable processing time in comparison with the state-of-the-art algorithms.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.