Evidence map›Paper›PMID 35734766›Full record

ArticleBiology methods & protocols2022

MLBioIGE: integration and interplay of machine learning and bioinformatics approach to identify the genetic effect of SARS-COV-2 on idiopathic pulmonary fibrosis patients.

Sk Tanzir Mehedi, Kawsar Ahmed, Francis M Bui, Musfikur Rahaman, Imran Hossain, Tareq Mahmud Tonmoy, Rakibul Alam Limon, Sobhy M Ibrahim, Mohammad Ali Moni

Open access · goldAbstract read
In one paragraph

Article in Biology methods & protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 4 institutions in 4 countries.

Sk Tanzir MehediDepartment of Information Technology, University of Information Technology and Sciences, Baridhara, Dhaka-1212, Bangladesh.ORCID https://orcid.org/0000-0003-4435-7856
Kawsar AhmedDepartment of Electrical and Computer Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.ORCID https://orcid.org/0000-0002-4034-9819
Francis M BuiDepartment of Electrical and Computer Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.ORCID https://orcid.org/0000-0002-8799-5965
Musfikur RahamanDepartment of Information Technology, University of Information Technology and Sciences, Baridhara, Dhaka-1212, Bangladesh.
Imran HossainDepartment of Information Technology, University of Information Technology and Sciences, Baridhara, Dhaka-1212, Bangladesh.
Tareq Mahmud TonmoyDepartment of Information Technology, University of Information Technology and Sciences, Baridhara, Dhaka-1212, Bangladesh.
Rakibul Alam LimonDepartment of Information Technology, University of Information Technology and Sciences, Baridhara, Dhaka-1212, Bangladesh.
Sobhy M IbrahimDepartment of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Mohammad Ali MoniFaculty of Health and Behavioural Sciences, School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, QLD 4072, Australia.ORCID https://orcid.org/0000-0003-0756-1006
University of Information Technology and Sciences · BDUniversity of Saskatchewan · CAKing Saud University · SAThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2, the virus that causes COVID-19, is a current concern for people worldwide. The virus has recently spread worldwide and is out of control in several countries, putting the outbreak into a terrifying phase. Machine learning with transcriptome analysis has advanced in recent years. Its outstanding performance in several fields has emerged as a potential option to find out how SARS-CoV-2 is related to other diseases. Idiopathic pulmonary fibrosis (IPF) disease is caused by long-term lung injury, a risk factor for SARS-CoV-2. In this article, we used a variety of combinatorial statistical approaches, machine learning, and bioinformatics tools to investigate how the SARS-CoV-2 affects IPF patients' complexity. For this study, we employed two RNA-seq datasets. The unique contributions include common genes identification to identify shared pathways and drug targets, PPI network to identify hub-genes and basic modules, and the interaction of transcription factors (TFs) genes and TFs-miRNAs with common differentially expressed genes also placed on the datasets. Furthermore, we used gene ontology and molecular pathway analysis to do functional analysis and discovered that IPF patients have certain standard connections with the SARS-CoV-2 virus. A detailed investigation was carried out to recommend therapeutic compounds for IPF patients affected by the SARS-CoV-2 virus.

Indexed as

COVID-19differentially expressed genesgene ontologyidiopathic pulmonary fibrosismachine learningSARS-CoV-2

Identifiers

PMID35734766
PMCPMC9210941
OpenAlexW4281833436

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.