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Aims and Scope

Aims & Scope

What This Journal Publishes

A peer-reviewed, open-access journal for the genomic and epigenomic drivers of cancer — from mechanism through to clinical translation.

Our Aim

We publish work that advances understanding of how genomic and epigenomic change drives malignancy, and how that understanding reaches patients. We value methodological rigour and reproducibility over novelty for its own sake, and we actively seek negative and confirmatory results where they are well powered. A study that closes a question is as valuable to us as one that opens it.

4
issues each year
18 days
median to first decision
0
charges of any kind
CC BY
authors keep copyright

Subject Areas

Discovery

Tumour evolution, epigenetic regulation, structural variation, single-cell and spatial genomics.

Translation

Biomarkers, liquid biopsy, early detection, therapeutic resistance and precision oncology.

Methods

Sequencing chemistry, computational pipelines, benchmarking studies and open analytical tooling.

Populations

Germline risk, ancestry-aware analysis, screening programmes and health-system implementation.

In Scope

  • Genome-wide and targeted studies of carcinogenesis and tumour progression
  • Epigenetic mechanisms including methylation, chromatin state and non-coding regulation
  • Single-cell, spatial and long-read approaches to tumour heterogeneity
  • Circulating tumour DNA and other minimally invasive diagnostics
  • Functional genomics, including CRISPR screens and synthetic-lethal interactions
  • Computational methods released with documented, runnable code
  • Germline and polygenic contributions to cancer susceptibility
  • Pharmacogenomics and mechanisms of acquired treatment resistance
  • Tumour–immune interaction where a genomic or transcriptomic readout is central
  • Benchmarking and reproducibility studies of established methods

Out of Scope

  • Case reports without a genomic or molecular component
  • Purely clinical trials with no accompanying molecular analysis
  • Re-analyses of public data that add no new interpretation
  • Studies where the underlying data cannot be shared
  • Cell-line-only work with no validation in primary material
  • Predictive models reported without an independent test set

Article Types

1

Research Article

Full-length original work. No fixed word limit; length should match the evidence.

2

Brief Report

A single, well-supported finding. Up to 2,500 words and three display items.

3

Review

Commissioned or proposed. Send an outline before writing a full submission.

4

Registered Report

Peer-reviewed before results exist; acceptance in principle survives the outcome.

Readership

Our readers are cancer biologists, computational scientists, pathologists and clinical oncologists. Write so that a competent researcher one field away can follow the argument: define abbreviations on first use, state what is new in the abstract, and keep the methods detailed enough to be repeated.

Not sure whether your work fits? Send a presubmission enquiry with your abstract through the Contact Us page and an editor will respond before you invest time in a full submission. We would rather answer a short question early than decline a finished manuscript late.

Ready to submit?

Read the Guide for Authors, then start your submission from the Submit Paper menu.