Evidence map›Paper›PMID 35409058›Full record

ArticleInternational journal of molecular sciences2022

Generative Adversarial Networks for Creating Synthetic Nucleic Acid Sequences of Cat Genome.

Debapriya Hazra, Mi-Ryung Kim, Yung-Cheol Byun

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Molecular Pharmacology at the Crossroads of Precision Medicine.Current issues in molecular biology · 2025
    Article
  3. Article
  4. Deep Generative Model-Driven Design of Microbial Synthetic Promoters.Journal of microbiology and biotechnology · 2025
    Review
  5. Article
  6. DeepBJournal of advanced research · 2025
    Article
  7. Article
  8. The Use of AI for Phenotype-Genotype Mapping.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  9. Progress of the "Molecular Informatics" Section in 2022.International journal of molecular sciences · 2023
    Article
  10. 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

3 authors at 2 institutions in 1 country.

Debapriya HazraDepartment of Computer Engineering, Jeju National University, Jeju 63243, Korea.
Mi-Ryung KimVeterinary Internal Medicine, Kyungpook National University, Daegu 41566, Korea.
Yung-Cheol ByunDepartment of Computer Engineering, Institute of Information Science & Technology, Jeju National University, Jeju 63243, Korea.ORCID 0000-0003-1107-9941
Jeju National University · KRKyungpook National University · KR

Funding

Jeju National University P0016977
6 · The paper itself

Abstract

Nucleic acids are the basic units of deoxyribonucleic acid (DNA) sequencing. Every organism demonstrates different DNA sequences with specific nucleotides. It reveals the genetic information carried by a particular DNA segment. Nucleic acid sequencing expresses the evolutionary changes among organisms and revolutionizes disease diagnosis in animals. This paper proposes a generative adversarial networks (GAN) model to create synthetic nucleic acid sequences of the cat genome tuned to exhibit specific desired properties. We obtained the raw sequence data from Illumina next generation sequencing. Various data preprocessing steps were performed using Cutadapt and DADA2 tools. The processed data were fed to the GAN model that was designed following the architecture of Wasserstein GAN with gradient penalty (WGAN-GP). We introduced a predictor and an evaluator in our proposed GAN model to tune the synthetic sequences to acquire certain realistic properties. The predictor was built for extracting samples with a promoter sequence, and the evaluator was built for filtering samples that scored high for motif-matching. The filtered samples were then passed to the discriminator. We evaluated our model based on multiple metrics and demonstrated outputs for latent interpolation, latent complementation, and motif-matching. Evaluation results showed our proposed GAN model achieved 93.7% correlation with the original data and produced significant outcomes as compared to existing models for sequence generation.

Indexed as

Adenosine DeaminaseImage Processing, Computer-AssistedDNAIntercellular Signaling Peptides and ProteinsAdenosine DeaminaseDNAIntercellular Signaling Peptides and Proteinscat genomegenerative adversarial networksmotif matchingnucleic acid sequencespromoter classificationpromoter predictionsynthetic genomeWGAN-GP

Identifiers

PMID35409058
PMCPMC8998662
OpenAlexW4221133435

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.