Evidence map›Paper›PMID 36290497›Full record

ArticleBioengineering (Basel, Switzerland)2022

Predicting Analyte Concentrations from Electrochemical Aptasensor Signals Using LSTM Recurrent Networks.

Fatemeh Esmaeili, Erica Cassie, Hong Phan T Nguyen, Natalie O V Plank, Charles P Unsworth, Alan Wang

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

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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

6 authors.

Fatemeh EsmaeiliDepartment of Engineering Science, University of Auckland, Auckland 1010, New Zealand.ORCID 0000-0002-1661-8409
Erica CassieSchool of Chemical and Physical Sciences, Victoria University of Wellington, Wellington 6021, New Zealand.ORCID 0000-0001-9755-9537
Hong Phan T NguyenSchool of Chemical and Physical Sciences, Victoria University of Wellington, Wellington 6021, New Zealand.
Natalie O V PlankSchool of Chemical and Physical Sciences, Victoria University of Wellington, Wellington 6021, New Zealand.ORCID 0000-0002-9798-9657
Charles P UnsworthDepartment of Engineering Science, University of Auckland, Auckland 1010, New Zealand.
Alan WangAuckland Bioengineering Institute, University of Auckland, Auckland 1010, New Zealand.

Funding

Royal Society of New Zealand 5000357
6 · The paper itself

Abstract

Nanomaterial-based aptasensors are useful devices capable of detecting small biological species. Determining suitable signal processing methods can improve the identification and quantification of target analytes detected by the biosensor and consequently improve the biosensor's performance. In this work, we propose a data augmentation method to overcome the insufficient amount of available original data and long short-term memory (LSTM) to automatically predict the analyte concentration from part of a signal registered by three electrochemical aptasensors, with differences in bioreceptors, analytes, and the signals' lengths for specific concentrations. To find the optimal network, we altered the following variables: the LSTM layer structure (unidirectional LSTM (LSTM) and bidirectional LSTM (BLSTM)), optimizers (Adam, RMSPROP, SGDM), number of hidden units, and amount of augmented data. Then, the evaluation of the networks revealed that the highest original data accuracy increased from 50% to 92% by exploiting the data augmentation method. In addition, the SGDM optimizer showed a lower performance prediction than that of the ADAM and RMSPROP algorithms, and the number of hidden units was ineffective in improving the networks' performances. Moreover, the BLSTM nets showed more accurate predictions than those of the ULSTM nets on lengthier signals. These results demonstrate that this method can automatically detect the analyte concentration from the sensor signals.

Indexed as

bidirectional LSTMclassificationdata augmentationdeep learninglong short-term memory neural networksmulti-class classifierstime-series aptasensor signalunidirectional LSTM

Identifiers

PMID36290497
PMCPMC9598695

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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.