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pmid:35846148

Predicting the Lung Adenocarcinoma and Its Biomarkers by Integrating Gene Expression and DNA Methylation Data.

Wang-Ren Qiu · Bei-Bei Qi · Wei-Zhong Lin · Shou-Hua Zhang · Wang-Ke Yu · Shun-Fa Huang

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.926927

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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title
Predicting the Lung Adenocarcinoma and Its Biomarkers by Integrating Gene Expression and DNA Methylation Data.
doi
10.3389/fgene.2022.926927
pmid
35846148
authors array · 6 items
[0]
Wang-Ren Qiu
[1]
Bei-Bei Qi
[2]
Wei-Zhong Lin
[3]
Shou-Hua Zhang
[4]
Wang-Ke Yu
[5]
Shun-Fa Huang
journal
Frontiers in genetics
year
2022
abstract
The early symptoms of lung adenocarcinoma patients are inapparent, and the clinical diagnosis of lung adenocarcinoma is primarily through X-ray examination and pathological section examination, whereas the discovery of biomarkers points out another direction for the diagnosis of lung adenocarcinoma with the development of bioinformatics technology. However, it is not accurate and trustworthy to diagnose lung adenocarcinoma due to omics data with high-dimension and low-sample size (HDLSS) features or biomarkers produced by utilizing only single omics data. To address the above problems, the feature selection methods of biological analysis are used to reduce the dimension of gene expression data (GSE19188) and DNA methylation data (GSE139032, GSE49996). In addition, the Cartesian product method is used to expand the sample set and integrate gene expression data and DNA methylation data. The classification is built by using a deep neural network and is evaluated on K-fold cross validation. Moreover, gene ontology analysis and literature retrieving are used to analyze the biological relevance of selected genes, TCGA database is used for survival analysis of these potential genes through Kaplan-Meier estimates to discover the detailed molecular mechanism of lung adenocarcinoma. Survival analysis shows that COL5A2 and SERPINB5 are significant for identifying lung adenocarcinoma and are considered biomarkers of lung adenocarcinoma.
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Five-fold cross validation is also used to obtain the average values of accuracy and AUROC.
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sections[11] "The Impact of Different Classifiers on Performance" paragraph 3
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Five-fold cross validation is also used to obtain the average values of accuracy and AUROC.
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DNA methylation profiling of lung adenocarcinomas and patient-matched non-malignant lung
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parameters object · 0 fields
data_shapes array · 1 item
[0]
count_matrix_with_condition
evidence object · 3 fields
score
0.8
band
high
quote
limma
[2] object · 10 fields
id
method-3
family
machine_learning
specific
random_forest
label
Machine learning
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
machine_learning_random_forest
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
0.8
band
high
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random forest
[3] object · 10 fields
id
method-4
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diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
dsl_operations array · 6 items
[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
score
0.8
band
high
quote
AUROC
[4] object · 10 fields
id
method-5
family
null
specific
null
label
five-fold cross validation
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Five-fold cross validation is also used to obtain the average values of accuracy and AUROC.
targets array · 0 items
gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 3 items
[0]
GSE19188
[1]
GSE139032
[2]
GSE49996
resolved_accessions array · 3 items
[0]
GSE19188
[1]
GSE139032
[2]
GSE49996
statements array · 1 item
[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
basis
The paper names GSE19188, GSE139032, GSE49996 in Comprehensive Gene Expression Omnibus of the National Center for Biotechnology Information and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
[0]
survival_km
assets array · 2 items
[0]
source:pmid:35846148
[1]
data:geo:GSE139032
steps array · 1 item
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run_analysis
must_build object · 5 fields
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converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE139032
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T17:55:46Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
12800
completion_tokens
1381
cached_tokens
256
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
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MiniMax-M3.1-Flash
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minimax
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review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
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absent
status
not_run
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null
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gaps array · 1 item
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execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:35846148
type
paper
label
pmid:35846148
[1] object · 3 fields
id
source:pmid:35846148
type
manuscript
label
PMID 35846148 full text
[2] object · 3 fields
id
data:geo:GSE139032
type
dataset
label
GEO GSE139032
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:35846148
type
paper
label
pmid:35846148
[1] object · 3 fields
id
source:pmid:35846148
type
manuscript
label
PMID 35846148 full text
[2] object · 3 fields
id
data:geo:GSE139032
type
dataset
label
GEO GSE139032
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-35846148
type
extraction
used array · 1 item
[0]
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agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE139032
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accession_resolution
used array · 1 item
[0]
data:geo:GSE139032
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
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software
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Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
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MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:35846148
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sha256:4a0ebd6bf1ce8c0b9833eaf35d229ffc1d94a2933615a23ffd7add1f249659f5
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null
gaps array · 11 items
[0]
asset:data:geo:GSE139032 licence not read
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asset:data:geo:GSE139032 not downloaded
[2]
asset:data:geo:GSE19188 licence not read
[3]
asset:data:geo:GSE19188 not downloaded
[4]
asset:data:geo:GSE49996 licence not read
[5]
asset:data:geo:GSE49996 not downloaded
[6]
execution.not_run
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method.reader_named_unmapped
[8]
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[9]
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assays array · 1 item
[0] object · 11 fields
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supported
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dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35846148", "kind": "science-record", "revision": 4, "content_hash": "sha256:cf4c677899033f0db9df5149f805e18489e250398ae10ff2049d2f3bbdcdcbd6", "created_at": "2026-11-01T18:14:55Z", "updated_at": "2026-11-01T22:07:03Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Predicting the Lung Adenocarcinoma and Its Biomarkers by Integrating Gene Expression and DNA Methylation Data.", "doi": "10.3389/fgene.2022.926927", "pmid": "35846148", "authors": ["Wang-Ren Qiu", "Bei-Bei Qi", "Wei-Zhong Lin", "Shou-Hua Zhang", "Wang-Ke Yu", "Shun-Fa Huang"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "The early symptoms of lung adenocarcinoma patients are inapparent, and the clinical diagnosis of lung adenocarcinoma is primarily through X-ray examination and pathological section examination, whereas the discovery of biomarkers points out another direction for the diagnosis of lung adenocarcinoma with the development of bioinformatics technology. However, it is not accurate and trustworthy to diagnose lung adenocarcinoma due to omics data with high-dimension and low-sample size (HDLSS) features or biomarkers produced by utilizing only single omics data. To address the above problems, the feature selection methods of biological analysis are used to reduce the dimension of gene expression data (GSE19188) and DNA methylation data (GSE139032, GSE49996). In addition, the Cartesian product method is used to expand the sample set and integrate gene expression data and DNA methylation data. The classification is built by using a deep neural network and is evaluated on K-fold cross validation. Moreover, gene ontology analysis and literature retrieving are used to analyze the biological relevance of selected genes, TCGA database is used for survival analysis of these potential genes through Kaplan-Meier estimates to discover the detailed molecular mechanism of lung adenocarcinoma. 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