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pmid:37662777

Prognostic value of GLCE and infiltrating immune cells in Ewing sarcoma.

Jian Wen · Lijun Yi · Lijia Wan · Xieping Dong

Heliyon · 2023 doi:10.1016/j.heliyon.2023.e19357

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:37662777
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2026-11-01T19:02:26Z
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2026-11-01T22:52:37Z
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paper object · 10 fields
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title
Prognostic value of GLCE and infiltrating immune cells in Ewing sarcoma.
doi
10.1016/j.heliyon.2023.e19357
pmid
37662777
authors array · 4 items
[0]
Jian Wen
[1]
Lijun Yi
[2]
Lijia Wan
[3]
Xieping Dong
journal
Heliyon
year
2023
abstract
Background: The prognostic value of D-glucuronyl C5-epimerase (GLCE) and mast cell infiltration in Ewing sarcoma (ES) has not been well specified and highlighted, which may facilitate survival prediction and treatment. Methods: Several qualified datasets were downloaded from the GEO website. Common differentially expressed genes between normal subjects and ES patients in GSE17679, GSE45544, and GSE68776 were identified and screened by multiple algorithms to find hub genes with prognostic value. The prognostic value of 64 infiltrating cells was also explored. A prognostic model was established and then validated with GSE63155 and GSE63156. Finally, functional analysis was performed. Results: GLCE and mast cell infiltration were screened as two indicators for a prognostic model. The Kaplan‒Meier analysis showed that patients in the low GLCE expression, mast cell infiltration and risk score groups had poorer outcomes than patients in the high GLCE expression, mast cell infiltration and risk score groups, both in the training and validation sets. Scatter plots and heatmaps also indicated the same results. The concordance indices and calibration analyses indicated a high prediction accuracy of the model in the training and validation sets. The time-dependent receiver operating characteristic analyses suggested high sensitivity and specificity of the model, with area under the curve values between 0.76 and 0.98. The decision curve analyses suggested a significantly higher net benefit by the model than the treat-all and treat-none strategies. Functional analyses suggested that glycosaminoglycan biosynthesis-heparan sulfate/heparin, the cell cycle and microRNAs in cancer were upregulated in ES patients. Conclusions: GLCE and mast cell infiltration are potential prognostic indicators in ES. GLCE may affect the proliferation, angiogenesis and metastasis of ES by affecting the biosynthesis of heparan sulfate and heparin.
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DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.
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sections[4] "Identification of common DEGs and prognostic genes" paragraph 2
quote
DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.
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Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.
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sections[24] "Data availability" paragraph 2
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Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.
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Inflammatory gene profiling of Ewing sarcoma family of tumors
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Ewing sarcoma compared to a normal body map
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Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions [EuroEwing]
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Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.
access_statement_kind
data_availability_statement
sample_accessions array · 74 items
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GSM1681080
[1]
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[2]
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[4]
GSM1681084
[5]
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[32]
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[39]
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[40]
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[41]
GSM1681121
[42]
GSM1681122
[43]
GSM1681123
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GSM1681124
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GSM1681125
[46]
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[48]
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[49]
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[50]
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[51]
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[54]
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[73]
GSM1681153
sample_count
74
group_sizes
null
group_sizes_basis
null
platform
5175
taxon
Homo sapiens
title
Exon array profiles of primary human Ewing sarcoma tumors
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 10 items
[0]
asset:data:geo:GSE17679 not downloaded
[1]
asset:data:geo:GSE17679 licence not read
[2]
asset:data:geo:GSE45544 not downloaded
[3]
asset:data:geo:GSE45544 licence not read
[4]
asset:data:geo:GSE63155 not downloaded
[5]
asset:data:geo:GSE63155 licence not read
[6]
asset:data:geo:GSE63156 not downloaded
[7]
asset:data:geo:GSE63156 licence not read
[8]
asset:data:geo:GSE68776 not downloaded
[9]
asset:data:geo:GSE68776 licence not read
analysis object · 4 fields
state
complete
methods array · 5 items
[0] object · 10 fields
id
method-1
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
dsl_operations array · 1 item
[0]
cox_ph
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
band
verbatim
quote
DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.
[1] object · 10 fields
id
method-2
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
quote
random forest
[2] object · 10 fields
id
method-3
family
network_analysis
specific
ppi_network
label
Network / pathway analysis
dsl_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
quote
PPI
[3] object · 10 fields
id
method-4
family
network_analysis
specific
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label
Network / pathway analysis
dsl_operations array · 1 item
[0]
pathway_enrich
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parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
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GO enrichment
[4] object · 10 fields
id
method-5
family
model_calibration
specific
decision_curve
label
Model calibration / clinical utility
dsl_operations array · 2 items
[0]
calibration_bins
[1]
net_benefit
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
predictions_and_outcomes
evidence object · 3 fields
score
0.7
band
medium
quote
net benefit
targets array · 0 items
gaps array · 0 items
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]
cox_ph
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: cox_proportional_hazards.
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 · 5 items
[0]
GSE17679
[1]
GSE68776
[2]
GSE45544
[3]
GSE63155
[4]
GSE63156
resolved_accessions array · 5 items
[0]
GSE17679
[1]
GSE68776
[2]
GSE45544
[3]
GSE63155
[4]
GSE63156
statements array · 1 item
[0]
Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.
basis
The paper names GSE17679, GSE68776, GSE45544, GSE63155, GSE63156 in Gene Expression Omnibus (GEO) 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]
cox_ph
assets array · 2 items
[0]
source:pmid:37662777
[1]
data:geo:GSE17679
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE17679
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
2026-11-01T18:52:10Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
15403
completion_tokens
2743
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
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review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
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null
runs array · 0 items
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:37662777
type
paper
label
pmid:37662777
[1] object · 3 fields
id
source:pmid:37662777
type
manuscript
label
PMID 37662777 full text
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id
data:geo:GSE17679
type
dataset
label
GEO GSE17679
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
id
pmid:37662777
type
paper
label
pmid:37662777
[1] object · 3 fields
id
source:pmid:37662777
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manuscript
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PMID 37662777 full text
[2] object · 3 fields
id
data:geo:GSE17679
type
dataset
label
GEO GSE17679
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-37662777
type
extraction
used array · 1 item
[0]
source:pmid:37662777
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE17679
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE17679
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agent:corpus-assay-engine
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[0] object · 3 fields
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agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
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software
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MiniMax literature reader
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reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:37662777
parent_hash
sha256:f9a289831f2c67999a53c5b18f3b94376899f2e6152ac6e6d8aecd9d30b603df
fork_of
null
gaps array · 14 items
[0]
asset:data:geo:GSE17679 licence not read
[1]
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[2]
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[3]
asset:data:geo:GSE45544 not downloaded
[4]
asset:data:geo:GSE63155 licence not read
[5]
asset:data:geo:GSE63155 not downloaded
[6]
asset:data:geo:GSE63156 licence not read
[7]
asset:data:geo:GSE63156 not downloaded
[8]
asset:data:geo:GSE68776 licence not read
[9]
asset:data:geo:GSE68776 not downloaded
[10]
execution.not_run
[11]
review.human_critique
[12]
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[13]
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assays array · 1 item
[0] object · 11 fields
role
analysis
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survival_analysis
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f2132e96ae6c7a4e
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cox_ph
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supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.
order_basis
analysis_only
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assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37662777", "kind": "science-record", "revision": 5, "content_hash": "sha256:6759e31ca3688827c652783445037e4412081bebf793125723ee36d3bcc6a70c", "created_at": "2026-11-01T19:02:26Z", "updated_at": "2026-11-01T22:52:37Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic value of GLCE and infiltrating immune cells in Ewing sarcoma.", "doi": "10.1016/j.heliyon.2023.e19357", "pmid": "37662777", "authors": ["Jian Wen", "Lijun Yi", "Lijia Wan", "Xieping Dong"], "journal": "Heliyon", "year": 2023, "abstract": "Background: The prognostic value of D-glucuronyl C5-epimerase (GLCE) and mast cell infiltration in Ewing sarcoma (ES) has not been well specified and highlighted, which may facilitate survival prediction and treatment.\nMethods: Several qualified datasets were downloaded from the GEO website. Common differentially expressed genes between normal subjects and ES patients in GSE17679, GSE45544, and GSE68776 were identified and screened by multiple algorithms to find hub genes with prognostic value. The prognostic value of 64 infiltrating cells was also explored. A prognostic model was established and then validated with GSE63155 and GSE63156. Finally, functional analysis was performed.\nResults: GLCE and mast cell infiltration were screened as two indicators for a prognostic model. The Kaplan‒Meier analysis showed that patients in the low GLCE expression, mast cell infiltration and risk score groups had poorer outcomes than patients in the high GLCE expression, mast cell infiltration and risk score groups, both in the training and validation sets. Scatter plots and heatmaps also indicated the same results. The concordance indices and calibration analyses indicated a high prediction accuracy of the model in the training and validation sets. The time-dependent receiver operating characteristic analyses suggested high sensitivity and specificity of the model, with area under the curve values between 0.76 and 0.98. The decision curve analyses suggested a significantly higher net benefit by the model than the treat-all and treat-none strategies. Functional analyses suggested that glycosaminoglycan biosynthesis-heparan sulfate/heparin, the cell cycle and microRNAs in cancer were upregulated in ES patients.\nConclusions: GLCE and mast cell infiltration are potential prognostic indicators in ES. GLCE may affect the proliferation, angiogenesis and metastasis of ES by affecting the biosynthesis of heparan sulfate and heparin.", "claims": [{"id": "claim-method", "statement": "DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37662777", "locator": "sections[4] \"Identification of common DEGs and prognostic genes\" paragraph 2", "quote": "DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37662777", "locator": "sections[24] \"Data availability\" paragraph 2", "quote": "Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37662777"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes."}}, {"id": "method-2", "family": "machine_learning", "specific": "random_forest", "label": "Machine learning", "dsl_operations": [], "missing_operations": ["machine_learning_random_forest"], "expressible": false, "parameters": {}, "data_shapes": ["labelled_feature_matrix"], "evidence": {"score": 0.8, "band": "high", "quote": "random forest"}}, {"id": "method-3", "family": "network_analysis", "specific": "ppi_network", "label": "Network / pathway analysis", "dsl_operations": ["build_graph", "centrality_scores", "pathway_enrich"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["edge_list"], "evidence": {"score": 0.8, "band": "high", "quote": "PPI"}}, {"id": "method-4", "family": "network_analysis", "specific": "pathway_enrichment", "label": "Network / pathway analysis", "dsl_operations": ["pathway_enrich"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["edge_list"], "evidence": {"score": 0.8, "band": "high", "quote": "GO enrichment"}}, {"id": "method-5", "family": "model_calibration", "specific": "decision_curve", "label": "Model calibration / clinical utility", "dsl_operations": ["calibration_bins", "net_benefit"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["predictions_and_outcomes"], "evidence": {"score": 0.7, "band": "medium", "quote": "net benefit"}}], "targets": [], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"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": {"tier": "R1", "reachable": true, "accessions": ["GSE17679", "GSE68776", "GSE45544", "GSE63155", "GSE63156"], "resolved_accessions": ["GSE17679", "GSE68776", "GSE45544", "GSE63155", "GSE63156"], "statements": ["Publicly available data sets were analyzed in this study. These data can be found at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68776, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45544, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63155, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63156."], "basis": "The paper names GSE17679, GSE68776, GSE45544, GSE63155, GSE63156 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["cox_ph"], "assets": ["source:pmid:37662777", "data:geo:GSE17679"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE17679"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T18:52:10Z", "independence": "single_reader"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 15403, "completion_tokens": 2743, "cached_tokens": 128}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:37662777", "type": "paper", "label": "pmid:37662777"}, {"id": "source:pmid:37662777", "type": "manuscript", "label": "PMID 37662777 full text"}, {"id": "data:geo:GSE17679", "type": "dataset", "label": "GEO GSE17679"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:37662777", "type": "paper", "label": "pmid:37662777"}, {"id": "source:pmid:37662777", "type": "manuscript", "label": "PMID 37662777 full text"}, {"id": "data:geo:GSE17679", "type": "dataset", "label": "GEO GSE17679"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-37662777", "type": "extraction", "used": ["source:pmid:37662777"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE17679", "type": "accession_resolution", "used": ["data:geo:GSE17679"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:37662777", "parent_hash": "sha256:f9a289831f2c67999a53c5b18f3b94376899f2e6152ac6e6d8aecd9d30b603df", "fork_of": null, "generation": 4}, "gaps": ["asset:data:geo:GSE17679 licence not read", "asset:data:geo:GSE17679 not downloaded", "asset:data:geo:GSE45544 licence not read", "asset:data:geo:GSE45544 not downloaded", "asset:data:geo:GSE63155 licence not read", "asset:data:geo:GSE63155 not downloaded", "asset:data:geo:GSE63156 licence not read", "asset:data:geo:GSE63156 not downloaded", "asset:data:geo:GSE68776 licence not read", "asset:data:geo:GSE68776 not downloaded", "execution.not_run", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes."], "order_basis": "analysis_only", "id": "assay:1"}]}