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pmid:37729607

A 12-gene panel in estimating hormone-treatment responses of castration-resistant prostate cancer patients generated using a combined analysis of bulk and single-cell sequencing data.

Juanlan Huang · Dale Liu · Jun Li · Jing Xu · Shaowei Dong · Hao Zhang

Annals of medicine · 2023 doi:10.1080/07853890.2023.2260387

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

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:37729607
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2026-11-01T19:02:34Z
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2026-11-01T22:52:45Z
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title
A 12-gene panel in estimating hormone-treatment responses of castration-resistant prostate cancer patients generated using a combined analysis of bulk and single-cell sequencing data.
doi
10.1080/07853890.2023.2260387
pmid
37729607
authors array · 6 items
[0]
Juanlan Huang
[1]
Dale Liu
[2]
Jun Li
[3]
Jing Xu
[4]
Shaowei Dong
[5]
Hao Zhang
journal
Annals of medicine
year
2023
abstract
BACKGROUND: Castration-resistant prostate cancer (CRPC) represents one type of advanced prostate cancer (PCa) with a median survival time of 1-2 years. Currently, there is a lack of reliable gene panels in predicting hormone treatment (HT) responses due to limited knowledge of CRPC-specific tumor-microenvironment (TME) characteristics. METHODS: In this study, we first screened for up-regulated genes in CRPC samples using bulk-sequencing data retrieved from TCGA online database, and further investigated the expression status of these genes in four sets of downloaded single-cell RNA sequencing (scRNAseq) data: GSE117403 containing 16 normal human prostate samples; GSE141445 containing 13 PCa samples; GSE176031 containing 11 PCa samples and GSE137829 containing 6 CRPC samples. RESULTS: We identified a series of CRPC-specific TME characteristics including an enriched number of PEG10+ neuroendocrine cells, elevated expression of PPIB/CCDC74A/GAPDH/AR genes in tumor cells, increased expression of FAP/TGFB1 in cancer-associated fibroblasts (CAFs), suppressed immune environment featured by enhanced M2 macrophage polarization, T cell exhaustion and increased number of regulatory B cells. We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = -0.47, p = 0.019). CONCLUSIONS: Based on these unique TME characteristics of CRPC, we established a prediction tool for estimating the duration of HT responses in PCa treatment. Our results suggest mechanisms by which prostate cancer becomes castrate resistant. Further study of PEG10 (and/or others) to evaluate therapeutic efficacy should be considered.
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To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples. Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup. Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package. ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function.
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sections[5] "Identification of differentially expressed genes" paragraph 2
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To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples.
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sections[7] "Similarity analysis using Pearson correlation method" paragraph 2
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Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup.
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sections[7] "Similarity analysis using Pearson correlation method" paragraph 2
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Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package.
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sections[13] "Receiver operating characteristic (ROC) analysis" paragraph 2
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ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function.
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We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).
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We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).
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We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).
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We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).
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Single-cell analysis of human primary prostate cancer reveals the heterogeneity of tumor-associated epithelial cell states
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To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples. Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup. Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package. ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function.
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data:geo:GSE117403
type
dataset
label
GEO GSE117403
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-37729607
type
extraction
used array · 1 item
[0]
source:pmid:37729607
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE117403
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE117403
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
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 object · 4 fields
parent_id
pmid:37729607
parent_hash
sha256:423a65352184277df9900b3349804f44892b3a3c24f09cbc4a7a09114d6bec32
fork_of
null
gaps array · 13 items
[0]
asset:data:geo:GSE117403 licence not read
[1]
asset:data:geo:GSE117403 not downloaded
[2]
asset:data:geo:GSE137829 licence not read
[3]
asset:data:geo:GSE137829 not downloaded
[4]
asset:data:geo:GSE141445 licence not read
[5]
asset:data:geo:GSE141445 not downloaded
[6]
asset:data:geo:GSE176031 licence not read
[7]
asset:data:geo:GSE176031 not downloaded
[8]
execution.not_run
[9]
method.reader_differs_from_extractor
[10]
review.human_critique
[11]
review.independent_reader
[12]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
differential_expression
definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples. Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup. Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package. ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37729607", "kind": "science-record", "revision": 5, "content_hash": "sha256:606ba4ba4d27cd1498e164f72aeaf33b2f0c0deefd63ba221b42f825741693dc", "created_at": "2026-11-01T19:02:34Z", "updated_at": "2026-11-01T22:52:45Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A 12-gene panel in estimating hormone-treatment responses of castration-resistant prostate cancer patients generated using a combined analysis of bulk and single-cell sequencing data.", "doi": "10.1080/07853890.2023.2260387", "pmid": "37729607", "authors": ["Juanlan Huang", "Dale Liu", "Jun Li", "Jing Xu", "Shaowei Dong", "Hao Zhang"], "journal": "Annals of medicine", "year": 2023, "abstract": "BACKGROUND: Castration-resistant prostate cancer (CRPC) represents one type of advanced prostate cancer (PCa) with a median survival time of 1-2 years. Currently, there is a lack of reliable gene panels in predicting hormone treatment (HT) responses due to limited knowledge of CRPC-specific tumor-microenvironment (TME) characteristics.\nMETHODS: In this study, we first screened for up-regulated genes in CRPC samples using bulk-sequencing data retrieved from TCGA online database, and further investigated the expression status of these genes in four sets of downloaded single-cell RNA sequencing (scRNAseq) data: GSE117403 containing 16 normal human prostate samples; GSE141445 containing 13 PCa samples; GSE176031 containing 11 PCa samples and GSE137829 containing 6 CRPC samples.\nRESULTS: We identified a series of CRPC-specific TME characteristics including an enriched number of PEG10+ neuroendocrine cells, elevated expression of PPIB/CCDC74A/GAPDH/AR genes in tumor cells, increased expression of FAP/TGFB1 in cancer-associated fibroblasts (CAFs), suppressed immune environment featured by enhanced M2 macrophage polarization, T cell exhaustion and increased number of regulatory B cells. We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = -0.47, p = 0.019).\nCONCLUSIONS: Based on these unique TME characteristics of CRPC, we established a prediction tool for estimating the duration of HT responses in PCa treatment. Our results suggest mechanisms by which prostate cancer becomes castrate resistant. Further study of PEG10 (and/or others) to evaluate therapeutic efficacy should be considered.", "claims": [{"id": "claim-method", "statement": "To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples. Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup. Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package. ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37729607", "locator": "sections[5] \"Identification of differentially expressed genes\" paragraph 2", "quote": "To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples."}, {"asset": "source:pmid:37729607", "locator": "sections[7] \"Similarity analysis using Pearson correlation method\" paragraph 2", "quote": "Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup."}, {"asset": "source:pmid:37729607", "locator": "sections[7] \"Similarity analysis using Pearson correlation method\" paragraph 2", "quote": "Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package."}, {"asset": "source:pmid:37729607", "locator": "sections[13] \"Receiver operating characteristic (ROC) analysis\" paragraph 2", "quote": "ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function."}], "state": "complete"}, {"id": "claim-data-access", "statement": "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.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37729607", "locator": "sections[28] \"Data availability statement\" paragraph 2", "quote": "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."}], "state": "complete"}, {"id": "claim-target-result", "statement": "We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).", "kind": "quantitative", "target": {"value": 0.78, "unit": "auc", "tolerance": null, "source": "We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019)."}, "evidence": [{"asset": "source:pmid:37729607", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "We further established a 12-gene panel using these characteristics and showed that this panel could separate CRPC samples from PCa samples (AUC of 0.78), and CRPC patients with higher panel scores tended to have treatment failure or progression (R = −0.47, p = 0.019).", "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:37729607"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE117403"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE117403"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37729607", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1080/07853890.2023.2260387", "sha256": "sha256:80178ddca97b5359ab3ec832aaea7a90b36231d173fee4819d2a511b343a7b20", "bytes": 52261, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1080/07853890.2023.2260387", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10512812", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE117403", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE117403", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE117403", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM3293873", "GSM3293874", "GSM3293875", "GSM3293876", "GSM3293877", "GSM3293878", "GSM3293879", "GSM3293880", "GSM3293881", "GSM3293882", "GSM3293883", "GSM3293884", "GSM3293885", "GSM3293886", "GSM3293887", "GSM3293888"], "sample_count": 16, "group_sizes": null, "group_sizes_basis": null, "platform": "18573", "taxon": "Homo sapiens", "title": "Single Cell RNA-sequencing of cell types isolated by FACS from normal human prostates", "resolution_checked_at": "2026-11-01T19:09:46Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE137829", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE137829", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE137829", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM4089151", "GSM4089152", "GSM4089153", "GSM4089154", "GSM4711414", "GSM4711415"], "sample_count": 6, "group_sizes": null, "group_sizes_basis": null, "platform": "24676", "taxon": "Homo sapiens", "title": "Single-cell analysis supports a luminal-neuroendocrine transdifferentiation in human prostate cancer", "resolution_checked_at": "2026-11-01T19:09:46Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE141445", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE141445", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE141445", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function."}}, {"id": "method-2", "family": "principal_component_analysis", "specific": "pca", "label": "Principal component analysis", "dsl_operations": ["pca_fit"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["wide_numeric_matrix"], "evidence": {"score": 0.8, "band": "high", "quote": "PCA"}}, {"id": "method-3", "family": "differential_expression", "specific": "limma_voom", "label": "Differential expression analysis", "dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["count_matrix_with_condition"], "evidence": {"score": 0.8, "band": "high", "quote": "Limma"}}, {"id": "method-4", "family": "correlation_analysis", "specific": "pearson", "label": "Correlation analysis", "dsl_operations": ["pearson_r"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["paired_numeric_columns"], "evidence": {"score": 0.8, "band": "high", "quote": "Pearson correlation"}}, {"id": "method-5", "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": 0.7, "band": "medium", "quote": "PPI"}}, {"id": "method-6", "family": "diagnostic_evaluation", "specific": "roc", "label": "Diagnostic test evaluation", "dsl_operations": ["confusion_counts", "roc_curve", "sensitivity_specificity", "solve_confusion_matrix", "classification_metrics", "published_precision_envelope"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["reference_standard_and_test"], "evidence": {"score": 0.8, "band": "high", "quote": "ROC analysis"}}], "targets": [{"id": "target-published-estimate", "claim_id": "claim-target-result", "operation": "build_graph", "expected_value": 0.78, "unit": "auc", "tolerance": null, "state": "complete", "note": "The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none."}, {"id": "target-published-estimate-p-value", "claim_id": "claim-target-result", "operation": "build_graph", "expected_value": 0.019, "unit": "p-value", "tolerance": null, "state": "complete", "note": "The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold."}], "gaps": ["method.reader_differs_from_extractor"]}, "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": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: deseq2."}, "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": ["GSE117403", "GSE141445", "GSE176031", "GSE137829"], "resolved_accessions": ["GSE117403", "GSE141445", "GSE176031", "GSE137829"], "statements": ["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 GSE117403, GSE141445, GSE176031, GSE137829 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "assets": ["source:pmid:37729607", "data:geo:GSE117403"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE117403"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T18:53:56Z", "independence": "single_reader"}, "evidence_check": {"method": "reordered", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 15274, "completion_tokens": 2467, "cached_tokens": 256}}, "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:37729607", "type": "paper", "label": "pmid:37729607"}, {"id": "source:pmid:37729607", "type": "manuscript", "label": "PMID 37729607 full text"}, {"id": "data:geo:GSE117403", "type": "dataset", "label": "GEO GSE117403"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:37729607", "type": "paper", "label": "pmid:37729607"}, {"id": "source:pmid:37729607", "type": "manuscript", "label": "PMID 37729607 full text"}, {"id": "data:geo:GSE117403", "type": "dataset", "label": "GEO GSE117403"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-37729607", "type": "extraction", "used": ["source:pmid:37729607"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE117403", "type": "accession_resolution", "used": ["data:geo:GSE117403"], "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:37729607", "parent_hash": "sha256:423a65352184277df9900b3349804f44892b3a3c24f09cbc4a7a09114d6bec32", "fork_of": null, "generation": 4}, "gaps": ["asset:data:geo:GSE117403 licence not read", "asset:data:geo:GSE117403 not downloaded", "asset:data:geo:GSE137829 licence not read", "asset:data:geo:GSE137829 not downloaded", "asset:data:geo:GSE141445 licence not read", "asset:data:geo:GSE141445 not downloaded", "asset:data:geo:GSE176031 licence not read", "asset:data:geo:GSE176031 not downloaded", "execution.not_run", "method.reader_differs_from_extractor", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["To screen for differentially expressed genes, we applied Deseq2 (R package) to raw-count reads of HT_YES and HT_NO samples. Data normalization among different datasets was performed using log2(CPM + 1), and mean expression values for all genes were calculated for each subgroup. Pearson correlation value between two subgroups was calculated using R cor.test() function and the correlation results between all subgroup combinations were visualized using R ‘pheatmap’ package. ROC analysis was performed using R package ‘ROCR’ and ‘pROC’, and the AUC (area under curves) values were calculated using auc() function."], "order_basis": "analysis_only", "id": "assay:1"}]}