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pmid:26484146

Whole blood gene expression profiling of neonates with confirmed bacterial sepsis.

Paul Dickinson · Claire L Smith · Thorsten Forster · Marie Craigon · Alan J Ross · Mizan R Khondoker · Alasdair Ivens · David J Lynn · Judith Orme · Allan Jackson · Paul Lacaze · Katie L Flanagan · Benjamin J Stenson · Peter Ghazal

Genomics data · 2015 doi:10.1016/j.gdata.2014.11.003

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complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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title
Whole blood gene expression profiling of neonates with confirmed bacterial sepsis.
doi
10.1016/j.gdata.2014.11.003
pmid
26484146
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[0]
Paul Dickinson
[1]
Claire L Smith
[2]
Thorsten Forster
[3]
Marie Craigon
[4]
Alan J Ross
[5]
Mizan R Khondoker
[6]
Alasdair Ivens
[7]
David J Lynn
[8]
Judith Orme
[9]
Allan Jackson
[10]
Paul Lacaze
[11]
Katie L Flanagan
[12]
Benjamin J Stenson
[13]
Peter Ghazal
journal
Genomics data
year
2015
abstract
Neonatal infection remains a primary cause of infant morbidity and mortality worldwide and yet our understanding of how human neonates respond to infection remains incomplete. Changes in host gene expression in response to infection may occur in any part of the body, with the continuous interaction between blood and tissues allowing blood cells to act as biosensors for the changes. In this study we have used whole blood transcriptome profiling to systematically identify signatures and the pathway biology underlying the pathogenesis of neonatal infection. Blood samples were collected from neonates at the first clinical signs of suspected sepsis alongside age matched healthy control subjects. Here we report a detailed description of the study design, including clinical data collected, experimental methods used and data analysis workflows and which correspond with data in Gene Expression Omnibus (GEO) data sets (GSE25504). Our data set has allowed identification of a patient invariant 52-gene classifier that predicts bacterial infection with high accuracy and lays the foundation for advancing diagnostic, prognostic and therapeutic strategies for neonatal sepsis.
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Per-gene hypotheses of differential expression between bacterial infection cases and control neonates were tested through linear modeling of the log2 scale expression values between groups and subsequent empirical Bayesian approaches to moderate the test statistic by pooling variance information from multiple genes (Bioconductor package ‘limma’ [4]).
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Per-gene hypotheses of differential expression between bacterial infection cases and control neonates were tested through linear modeling of the log2 scale expression values between groups and subsequent empirical Bayesian approaches to moderate the test statistic by pooling variance information from multiple genes (Bioconductor package ‘limma’ [4]).
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Here we report a detailed description of the study design, including clinical data collected, experimental methods used and data analysis workflows and which correspond with data in Gene Expression Omnibus (GEO) data sets (GSE25504).
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Our data set has allowed identification of a patient invariant 52-gene classifier that predicts bacterial infection with high accuracy and lays the foundation for advancing diagnostic, prognostic and therapeutic strategies for neonatal sepsis.
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Whole blood mRNA expression profiling of host molecular networks in neonatal sepsis
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A case–control gene expression profiling study of whole blood taken from neonates at the first clinical sign of sepsis and control healthy neonates. Study includes training and replication sets for blood culture positive samples and clinical evaluation set of blood culture negative sepsis cases. Results compared blood culture or cerebrospinal fluid positive septic neonates, blood culture negative septic neonates and healthy control neonates. Prior power calculations were based on Healthy Edinburgh neonates using the CodeLink platform and Gambian infants (9 months of age) were used for further refinement of power calculations using Illumina HT-12 platform.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:26484146", "kind": "science-record", "revision": 8, "content_hash": "sha256:d599eb97a401f88ff399d317f2790f321301baed7465989d239ae4e73e332cda", "created_at": "2026-11-01T15:40:12Z", "updated_at": "2026-11-01T22:42:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Whole blood gene expression profiling of neonates with confirmed bacterial sepsis.", "doi": "10.1016/j.gdata.2014.11.003", "pmid": "26484146", "authors": ["Paul Dickinson", "Claire L Smith", "Thorsten Forster", "Marie Craigon", "Alan J Ross", "Mizan R Khondoker", "Alasdair Ivens", "David J Lynn", "Judith Orme", "Allan Jackson", "Paul Lacaze", "Katie L Flanagan", "Benjamin J Stenson", "Peter Ghazal"], "journal": "Genomics data", "year": 2015, "abstract": "Neonatal infection remains a primary cause of infant morbidity and mortality worldwide and yet our understanding of how human neonates respond to infection remains incomplete. Changes in host gene expression in response to infection may occur in any part of the body, with the continuous interaction between blood and tissues allowing blood cells to act as biosensors for the changes. In this study we have used whole blood transcriptome profiling to systematically identify signatures and the pathway biology underlying the pathogenesis of neonatal infection. Blood samples were collected from neonates at the first clinical signs of suspected sepsis alongside age matched healthy control subjects. Here we report a detailed description of the study design, including clinical data collected, experimental methods used and data analysis workflows and which correspond with data in Gene Expression Omnibus (GEO) data sets (GSE25504). Our data set has allowed identification of a patient invariant 52-gene classifier that predicts bacterial infection with high accuracy and lays the foundation for advancing diagnostic, prognostic and therapeutic strategies for neonatal sepsis.", "claims": [{"id": "claim-method", "statement": "Per-gene hypotheses of differential expression between bacterial infection cases and control neonates were tested through linear modeling of the log2 scale expression values between groups and subsequent empirical Bayesian approaches to moderate the test statistic by pooling variance information from multiple genes (Bioconductor package ‘limma’ [4]).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:26484146", "locator": "sections[9] \"Data normalization and analysis\" paragraph 5", "quote": "Per-gene hypotheses of differential expression between bacterial infection cases and control neonates were tested through linear modeling of the log2 scale expression values between groups and subsequent empirical Bayesian approaches to moderate the test statistic by pooling variance information from multiple genes (Bioconductor package ‘limma’ [4])."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Deposited data are available here: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE25504.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:26484146", "locator": "sections[2] \"Direct link to deposited data\" paragraph 2", "quote": "Deposited data are available here: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE25504."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified a patient-invariant 52-gene classifier that predicts bacterial infection with high accuracy, using whole-blood transcriptome data deposited in Gene Expression Omnibus as GSE25504.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:26484146", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Here we report a detailed description of the study design, including clinical data collected, experimental methods used and data analysis workflows and which correspond with data in Gene Expression Omnibus (GEO) data sets (GSE25504)."}, {"asset": "source:pmid:26484146", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Our data set has allowed identification of a patient invariant 52-gene classifier that predicts bacterial infection with high accuracy and lays the foundation for advancing diagnostic, prognostic and therapeutic strategies for neonatal sepsis."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified a patient-invariant 52-gene classifier that predicts bacterial infection with high accuracy, using whole-blood transcriptome data deposited in Gene Expression Omnibus as GSE25504.", "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:26484146"], "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:GSE25504"], "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:GSE25504"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:26484146", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.gdata.2014.11.003", "sha256": 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{"id": "asset:table:pmid:26484146:1", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:dd856033b2e9bcbba1025c9dd8b45bd3157d64d2641989f1701ff73be93bc156", "bytes": 2140, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[1]/table-wrap[1]#t0015", "version": null, "note": null, "structure": {"pmcid": "PMC4535963", "section_index": 1, "section_title": "Introduction", "row_count": 9, "column_count": 2}, "table": {"label": null, "caption": null, "rows": [["Specifications"], ["Organism/cell line/tissue", "Homo sapiens/whole blood"], ["Sex", "Male and female"], ["Sequencer or array type", "Illumina HT-12V3.0 Whole Human Genome microarray, CodeLink 55K Whole Human Genome microarray, Affymetrix U219 Whole Human Genome microarray and Affymetrix HG U133 Plus 2.0 Whole Human Genome microarray"], ["Data format", "Raw data (Tab delimited text files of background 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Study includes training and replication sets for blood culture positive samples and clinical evaluation set of blood culture negative sepsis cases. Results compared blood culture or cerebrospinal fluid positive septic neonates, blood culture negative septic neonates and healthy control neonates. Prior power calculations were based on Healthy Edinburgh neonates using the CodeLink platform and Gambian infants (9 months of age) were used for further refinement of power calculations using Illumina HT-12 platform."], ["Consent", "Written informed consent was obtained from parents of all enrolled infants in accordance with approval granted by the Lothian Research Ethics Committee for blood samples for RNA isolation obtained at the first time of clinical signs of suspected sepsis (reference 05/s1103/3). Samples obtained from The Gambia conformed to MRC policy regarding ethical research in children and were approved by the local scientific coordinating committee (SCC), the Joint Gambia Government/MRC Ethics Committee and by the London School of Hygiene and Tropical Medicine Ethics Committee (reference SCC1085 Pilot Study 1 (L2008.63))"], ["Sample source location", "Edinburgh, UK and The Gambia"]], "row_count": 9, "column_count": 2, "numeric_cells": 3, "header_rows": 1, "locator": "section[1]/table-wrap[1]#t0015"}}], "gaps": ["asset:data:geo:GSE25504 not downloaded", "asset:data:geo:GSE25504 licence not read"]}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "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": 1.0, "band": "verbatim", "quote": "Per-gene hypotheses of differential expression between bacterial infection cases and control neonates were tested through linear modeling of the log2 scale expression values between groups and subsequent empirical Bayesian approaches to moderate the test statistic by pooling variance information from multiple genes (Bioconductor package ‘limma’ [4])."}}], "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": ["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: limma_voom."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. 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