Evidence map›Paper›PMID 35720914›Full record

ArticleComputational intelligence and neuroscience2022

Multiclass Cancer Prediction Based on Copy Number Variation Using Deep Learning.

Haleema Attique, Sajid Shah, Saima Jabeen, Fiaz Gul Khan, Ahmad Khan, Mohammed ELAffendi

Open access · hybridAbstract read
In one paragraph

Article in Computational intelligence and neuroscience, 2022. 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
1.3field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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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

6 authors at 3 institutions in 2 countries.

Haleema AttiqueDepartment of Computer Science, COMSATS University Islamabad, Abbottabad Campus, Islamabad, Pakistan.
Sajid ShahDepartment of Computer Science, COMSATS University Islamabad, Abbottabad Campus, Islamabad, Pakistan.ORCID https://orcid.org/0000-0001-6334-4773
Saima JabeenDepartment of IT and Computer Science, Pak-Austria Facchochschule: Institute of Applied Sciences and Technology, Mang, Haripur, KPK, Pakistan.
Fiaz Gul KhanDepartment of Computer Science, COMSATS University Islamabad, Abbottabad Campus, Islamabad, Pakistan.
Ahmad KhanDepartment of Computer Science, COMSATS University Islamabad, Abbottabad Campus, Islamabad, Pakistan.
Mohammed ELAffendiEIAS Data Science Lab, College of Computer and Information Sciences, Prince Sultan University, Riyadh, Saudi Arabia.ORCID https://orcid.org/0000-0001-9349-1985
COMSATS University Islamabad · PKPrince Sultan University · SAPak-Austria Fachhochschule: Institute of Applied Sciences and Technology · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA copy number variation (CNV) is the type of DNA variation which is associated with various human diseases. CNV ranges in size from 1 kilobase to several megabases on a chromosome. Most of the computational research for cancer classification is traditional machine learning based, which relies on handcrafted extraction and selection of features. To the best of our knowledge, the deep learning-based research also uses the step of feature extraction and selection. To understand the difference between multiple human cancers, we developed three end-to-end deep learning models, i.e., DNN (fully connected), CNN (convolution neural network), and RNN (recurrent neural network), to classify six cancer types using the CNV data of 24,174 genes. The strength of an end-to-end deep learning model lies in representation learning (automatic feature extraction). The purpose of proposing more than one model is to find which architecture among them performs better for CNV data. Our best model achieved 92% accuracy with an ROC of 0.99, and we compared the performances of our proposed models with state-of-the-art techniques. Our models have outperformed the state-of-the-art techniques in terms of accuracy, precision, and ROC. In the future, we aim to work on other types of cancers as well.

Indexed as

Deep LearningNeoplasmsDNA Copy Number VariationsHumansMachine LearningNeural Networks, Computer

Identifiers

PMID35720914
PMCPMC9203194
OpenAlexW4285740467

What OpenQuestion holds

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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.