Evidence map›Paper›PMID 36359579›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Multi-Stage Temporal Convolution Network for COVID-19 Variant Classification.

Waseem Ullah, Amin Ullah, Khalid Mahmood Malik, Abdul Khader Jilani Saudagar, Muhammad Badruddin Khan, Mozaherul Hoque Abul Hasanat, Abdullah AlTameem, Mohammed AlKhathami

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

8 authors.

Waseem UllahDepartment of Software, Sejong University, Seoul 05006, Korea.
Amin UllahCORIS Institute, Oregon State University, Corvallis, OR 97331, USA.ORCID 0000-0001-7538-2689
Khalid Mahmood MalikDepartment of Computer Science and Engineering, Oakland University, Rochester, MI 48309, USA.ORCID 0000-0002-7927-3436
Abdul Khader Jilani SaudagarInformation Systems Department, College of Computer and Information Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11564, Saudi Arabia.ORCID 0000-0003-4205-3621
Muhammad Badruddin KhanInformation Systems Department, College of Computer and Information Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11564, Saudi Arabia.ORCID 0000-0002-4628-3240
Mozaherul Hoque Abul HasanatInformation Systems Department, College of Computer and Information Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11564, Saudi Arabia.ORCID 0000-0001-7948-6266
Abdullah AlTameemInformation Systems Department, College of Computer and Information Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11564, Saudi Arabia.
Mohammed AlKhathamiInformation Systems Department, College of Computer and Information Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11564, Saudi Arabia.

Funding

The Deputyship for Research & Innovation project number 959
6 · The paper itself

Abstract

The outbreak of the novel coronavirus disease COVID-19 (SARS-CoV-2) has developed into a global epidemic. Due to the pathogenic virus's high transmission rate, accurate identification and early prediction are required for subsequent therapy. Moreover, the virus's polymorphic nature allows it to evolve and adapt to various environments, making prediction difficult. However, other diseases, such as dengue, MERS-CoV, Ebola, SARS-CoV-1, and influenza, necessitate the employment of a predictor based on their genomic information. To alleviate the situation, we propose a deep learning-based mechanism for the classification of various SARS-CoV-2 virus variants, including the most recent, Omicron. Our model uses a neural network with a temporal convolution neural network to accurately identify different variants of COVID-19. The proposed model first encodes the sequences in the numerical descriptor, and then the convolution operation is applied for discriminative feature extraction from the encoded sequences. The sequential relations between the features are collected using a temporal convolution network to classify COVID-19 variants accurately. We collected recent data from the NCBI, on which the proposed method outperforms various baselines with a high margin.

Indexed as

artificial intelligenceCOVID-19deep learninggenomes sequence analysisvariant classification

Identifiers

PMID36359579
PMCPMC9689740

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.