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Methods & technologies

Methods are selected by the questions they can answer

This is a capability and study-design framework, not a claim that every method is currently available or in active use. Final selection depends on verified expertise, host resources and research design.

Question-led selectionCapability under verificationValidation by design

Method architecture

Thirteen method families across measurement and inference

Each card separates what a method measures, why it may be relevant and the class of question it can address.

01

Genomic Measurement

Genomic Measurement

Next Generation Sequencing

Measures
Nucleic-acid sequence at scale across genomes and transcriptomes.
Relevance
Provides quantitative material for genomic and transcriptomic analysis.
Research question
Which sequence-level features track biological variation?

Genomic Measurement

Genomics

Measures
Genome-wide variation and structural organisation.
Relevance
Supports analysis of inherited and acquired genomic variation.
Research question
How might genomic variation shape aging trajectories?

Genomic Measurement

Transcriptomics

Measures
RNA abundance across genes, isoforms and conditions.
Relevance
Captures regulatory state and cellular response.
Research question
Which regulatory programmes vary across age and state?
02

Molecular Measurement

Molecular Measurement

Proteomics

Measures
Protein abundance, modification and complex composition.
Relevance
Connects molecular composition more directly to cellular function.
Research question
Which proteome changes precede functional decline?
03

Resolution

Resolution

Single-Cell Analysis

Measures
Molecular state at the resolution of individual cells.
Relevance
Resolves heterogeneity hidden in bulk measurements.
Research question
Which cell populations contribute to tissue-level phenotypes?

Resolution

Spatial Omics

Measures
Molecular profiles that retain tissue coordinates.
Relevance
Preserves the spatial context in which mechanisms operate.
Research question
How is molecular variation distributed within tissue architecture?
04

Structure & Physics

Structure & Physics

Structural Biology

Measures
Three-dimensional structures of biomolecules and complexes.
Relevance
Provides a mechanistic basis for structure–function reasoning.
Research question
How does structural change alter functional capacity?

Structure & Physics

Molecular Biophysics

Measures
Stability, dynamics, kinetics and interaction energetics.
Relevance
Quantifies the physical basis of molecular behaviour.
Research question
Which biophysical parameters distinguish resilient states?
05

Computation

Computation

Bioinformatics

Measures
Derived quantities from large-scale biological datasets.
Relevance
Makes high-dimensional data reproducibly analysable.
Research question
Which analytical pipelines yield stable, interpretable signals?

Computation

Network Biology

Measures
Topology and dynamics of molecular interaction networks.
Relevance
Places individual measurements into a systems context.
Research question
How does network organisation buffer perturbation?

Computation

Machine Learning

Measures
Statistical structure and predictive relationships in data.
Relevance
Can detect complex patterns when validity and interpretability are controlled.
Research question
Can predictive models remain mechanistically interpretable?
06

Inference

Inference

Biostatistics

Measures
Effect size, uncertainty and inferential validity.
Relevance
Defines the evidence required to support a scientific claim.
Research question
What design supports a defensible causal conclusion?

Inference

Data Integration

Measures
Joint structure across heterogeneous data modalities.
Relevance
Connects separate measurement layers into one analytical framework.
Research question
How can layers be integrated without inflating false discovery?

Measurement validity

Does the assay measure the biological quantity required by the hypothesis?

Inference validity

Can the analysis distinguish uncertainty, prediction and causal interpretation?

Independent validation

Can central findings be challenged with orthogonal data or methodology?