Making sense of the regulatory genome.
Cis-regulatory elements at cellular resolution.
Is enhancer-driven gene regulation all wrapped up?
Regulatory genomics at biobank scales.
Predicting the regulatory genome.
Regulatory genome annotation.
RNA splicing - a central layer of gene regulation.
The effects of loss of Y chromosome on male health.
The therapeutic potential of circular RNAs.
Epigenetics and individuality: from concepts to causality across timescales.
A phylogenetic approach to comparative genomics.
Diversity and consequences of structural variation in the human genome.
Profiling the total transcriptome of single nuclei in archived samples with snRandom-seq.
Indirect recognition of pathogen virulence proteins to activate plant immune receptors.
Epigenetic ageing clocks: statistical methods and emerging computational challenges.
From genome to drug: the hidden story of diversity.
The genesis of paleogenetics.
Emerging roles of transcriptional condensates as temporal signal integrators.
X-linked competition - implications for human development and disease.
Simultaneous single-cell sequencing of RNA and DNA at scale with DEFND-seq.
Genomics of schizophrenia, bipolar disorder and major depressive disorder.
A crossroads in the timeline of human evolution.
Measuring the effects of regulatory variants in an endogenous context.
RNA polymerase II transcription compartments - from factories to condensates.
Spatial multi-omics of nuclear architecture with two-layer seqFISH.
Author Correction: Evolution and regulation of animal sex chromosomes.
Non-retroviral RNA viruses in eukaryotic genomes.
The evolutionary foundations of transcriptional regulation in animals.
When cellular reprogramming meets AI: towards de novo cell design.
Experimental evolution in an era of molecular manipulation.
An evolutionary continuum between non-coding and coding DNA.
Multiplexed assays of variant effect for clinical variant interpretation.
Viromics approaches for the study of viral diversity and ecology in microbiomes.
Towards improved fine-mapping of candidate causal variants.
Integrating the genome and exposome for precision health in Kuwait.
Rethinking life through digital evolution.
Prompt-based bioinformatics: a new interface for multi-omics analysis.
Tracing the evolution of sequencing into the era of genomic medicine.
Harnessing functional annotation to improve the accuracy and transferability of polygenic scores.
Collaborating at the nexus of genomics, humanities, social science and stakeholders.
A genomic view of Earth's biomes.
A clinical milestone for CRISPR in sickle-cell disease.
Advances in haplotype phasing and genotype imputation.
Spatial metabolomics to unravel cellular metabolism
The early days of transcriptome sequencing and functional genomics: Transcriptomics
The hidden diversity of tumours: Cancer genetics
Cytoplasmic mRNA decay and quality control machineries in eukaryotes
Spatial miRNomics: towards the integration of microRNAs in spatial biology
Integrating ELSI study teams in paediatric genomic research efforts
Genomic data sharing: you don’t know what you’ve got (till it’s gone)