Evidence map›Paper›PMID 39369547›Full record

ArticleComputers in biology and medicine2024

HIV-1 M group subtype classification using deep learning approach.

Sihua Peng

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

1 author.

Sihua PengDepartment of Epidemiology and Biostatistics, College of Public Health, University of Georgia, Athens, GA, 30602, United States. Electronic address: Sihua.Peng@uga.edu.

Funding

A de novo approach to detect and interrogate neglected HIV diversityR21AI165253 · NIAID · UNIVERSITY OF GEORGIA · PI ZHANG, MING · 2022 to 2023
$415k
NIAID NIH HHS R21 AI165253
6 · The paper itself

Abstract

Traditionally, the classification of HIV-1 M group subtypes has depended on statistical methods constrained by sample sizes. Here HIV-1-M-SPBEnv was proposed as the first deep learning-based method for classifying HIV-1 M group subtypes via env gene sequences. This approach overcomes sample size challenges by utilizing artificial molecular evolution techniques to generate a synthetic dataset suitable for machine learning. Employing a convolutional Autoencoder embedded with two residual blocks and two transpose residual blocks, followed by a full connected neural network block, HIV-1-M-SPBEnv simplifies complex, high-dimensional DNA sequence data into concise, information-rich, low-dimensional representations, achieving exceptional classification accuracy. Through independent data set validation, the precision, accuracy, recall and F1 score of the HIV-1-M-SPBEnv model predictions were all 100 %, confirming its capability to accurately identify all 12 subtypes of the HIV-1 M group. Deployed through a web server, it provides seamless HIV-1 M group subtype prediction capabilities for researchers and clinicians. HIV-1-M-SPBEnv web server is accessible at http://www.hivsubclass.com and all the code is available at https://github.com/pengsihua2023/HIV-1-M-SPBEnv.

Indexed as

Deep LearningHIV-1HIV InfectionsHumansNeural Networks, ComputerAIDSAutoencoderClassificationDeep learningHIV

Identifiers

PMID39369547
PMCPMC12208307

What Socratic holds

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Registered trials

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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 Socratic graph.