ArticleJournal of the American Medical Informatics Association : JAMIA
'N-of-1-pathways' unveils personal deregulated mechanisms from a single pair of RNA-Seq samples: towards precision medicine.
Article in Journal of the American Medical Informatics Association : JAMIA. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.
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Who cites it
34 citing papers in PubMed, 43 citations in OpenAlex.
- Baricitinib-associated changes in global gene expression during a 24-week phase II clinical systemic lupus erythematosus trial implicates a mechanism of action through multiple immune-related pathways.Lupus science & medicine · 2020Trial
- Functional Depth Biomarkers Distinguish Lung Squamous Cell Carcinoma from Lung Adenocarcinoma.Research square · 2026Article
- Paired-Sample and Pathway-Anchored MLOps Framework for Robust Transcriptomic Machine Learning in Small Cohorts: Model Classification Study.JMIR bioinformatics and biotechnology · 2025Article
- FUSION: a family-level integration approach for robust differential analysis of small non-coding RNAs.Bioinformatics (Oxford, England) · 2025Article
- Evaluation of single-sample network inference methods for precision oncology.NPJ systems biology and applications · 2024Article
- Unlocking immune-mediated disease mechanisms with transcriptomics.Biochemical Society transactions · 2021Review
- Hypoxia-Inducible Factor 2-Alpha Mediated Gene Sets Differentiate Pulmonary Arterial Hypertension.Frontiers in cell and developmental biology · 2021Article
- Personalized beyond Precision: Designing Unbiased Gold Standards to Improve Single-Subject Studies of Personal Genome Dynamics from Gene Products.Journal of personalized medicine · 2020Article
- binomialRF: interpretable combinatoric efficiency of random forests to identify biomarker interactions.BMC bioinformatics · 2020Article
- Causal network perturbations for instance-specific analysis of single cell and disease samples.Bioinformatics (Oxford, England) · 2020Article
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- Module Analysis Using Single-Patient Differential Expression Signatures Improves the Power of Association Studies for Alzheimer's Disease.Frontiers in genetics · 2020Article
- Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine.BMC medical genomics · 2019Article
- Developing a 'personalome' for precision medicine: emerging methods that compute interpretable effect sizes from single-subject transcriptomes.Briefings in bioinformatics · 2019Review
- Interpretation of 'Omics dynamics in a single subject using local estimates of dispersion between two transcriptomes.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2019Article
- A Single-Subject Method to Detect Pathways Enriched With Alternatively Spliced Genes.Frontiers in genetics · 2019Article
- Testing for differentially expressed genetic pathways with single-subject N-of-1 data in the presence of inter-gene correlation.Statistical methods in medical research · 2018Article
- Unmet Needs in Systemic Sclerosis Understanding and Treatment: the Knowledge Gaps from a Scientist's, Clinician's, and Patient's Perspective.Clinical reviews in allergy & immunology · 2018Review
- The Emerging Potential for Network Analysis to Inform Precision Cancer Medicine.Journal of molecular biology · 2018Review
- Emergence of pathway-level composite biomarkers from converging gene set signals of heterogeneous transcriptomic responses.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018Article
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Authors and funding
12 authors at 3 institutions in 2 countries.
Funding
Abstract
backgroundThe emergence of precision medicine allowed the incorporation of individual molecular data into patient care. Indeed, DNA sequencing predicts somatic mutations in individual patients. However, these genetic features overlook dynamic epigenetic and phenotypic response to therapy. Meanwhile, accurate personal transcriptome interpretation remains an unmet challenge. Further, N-of-1 (single-subject) efficacy trials are increasingly pursued, but are underpowered for molecular marker discovery.
method'N-of-1-pathways' is a global framework relying on three principles: (i) the statistical universe is a single patient; (ii) significance is derived from geneset/biomodules powered by paired samples from the same patient; and (iii) similarity between genesets/biomodules assesses commonality and differences, within-study and cross-studies. Thus, patient gene-level profiles are transformed into deregulated pathways. From RNA-Seq of 55 lung adenocarcinoma patients, N-of-1-pathways predicts the deregulated pathways of each patient.
resultsCross-patient N-of-1-pathways obtains comparable results with conventional genesets enrichment analysis (GSEA) and differentially expressed gene (DEG) enrichment, validated in three external evaluations. Moreover, heatmap and star plots highlight both individual and shared mechanisms ranging from molecular to organ-systems levels (eg, DNA repair, signaling, immune response). Patients were ranked based on the similarity of their deregulated mechanisms to those of an independent gold standard, generating unsupervised clusters of diametric extreme survival phenotypes (p=0.03).
conclusionsThe N-of-1-pathways framework provides a robust statistical and relevant biological interpretation of individual disease-free survival that is often overlooked in conventional cross-patient studies. It enables mechanism-level classifiers with smaller cohorts as well as N-of-1 studies. SOFTWARE: http://lussierlab.org/publications/N-of-1-pathways.
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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.