Evidence map›Paper›PMID 39544183›Full record

ReviewJournal of biological methods2024

Cancer genetics and deep learning applications for diagnosis, prognosis, and categorization.

Massoud Sokouti, Babak Sokouti

Abstract readReview
In one paragraph

Review in Journal of biological methods, 2024. 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. Review
  2. Review
  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

2 authors.

Massoud SokoutiResearch Center of Evidence-Based Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Babak SokoutiBiotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression data are used to discover meaningful hidden information in gene datasets. Cancer and other disorders may be diagnosed based on differences in gene expression profiles, and this information can be gleaned by gene sequencing. Thanks to the tremendous power of artificial intelligence (AI), healthcare has become a significant user of deep learning (DL) for predicting cancer diseases and categorizing gene expression. Gene expression Microarrays have been proved effective in predicting cancer diseases and categorizing gene expression. Gene expression datasets contain only limited samples, but the features of cancer are diverse and complex. To overcome their dimensionality, gene expression datasets must be enhanced. By learning and analyzing features of input data, it is possible to extract features, as multidimensional arrays, from the data. Synthetic samples are needed to strengthen the range of information. DL strategies may be used when gene expression data are used to diagnose and classify cancer diseases.

Indexed as

CancerDeep learningGene expressionHigh dimensionality

Identifiers

PMID39544183
PMCPMC11557296

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.