Microbial ecology and evolution in the genomics era
Ancient DNA insights into diverse pathogens and their hosts
Bringing methylation profile scores to early life.
Regulation of gene expression by alternative polyadenylation in health and disease.
Long non-coding RNAs as orchestrators of dosage compensation.
Emergence and evolution of protein-coding de novo genes.
Interpretation, extrapolation and perturbation of single cells
Let the data speak — single-cell analysis with CellWhisperer
A genomic and epigenomic view of human centromeres
Ancestral diversity in complex disease genetics: from discovery to translation
From models to molecules: self-organized and instructed modes of developmental patterning
Mapping the disease interactome
Proteoform medicine: characterizing and targeting protein forms in human disease
Whole-genome spatial transcriptomic imaging with RAEFISH
Monitoring biological effects of somatic cell genome editing
Bridging behaviour and genomics for tsetse fly control
High-throughput identification of aptamer–target pairs with SPARK-seq
The genetic foundations of convergent traits
Revisiting the blueprint for an interpretable virtual cell
Revisiting the molecular workhorse: plasmids in evolutionary conflict
Navigating ethical, legal and social implications in genomic newborn screening
Massively parallel reporter assays: from barcodes to biology
Annotating genomes at increased scale and resolution
A codon-resolved view of subcellular translation with LOCL-TL
Evolutionary causes and consequences of gene duplication
Bridging technical innovation and computational advances in studies of RNA–protein assemblies
From DNA microarrays to somatic mosaicism in population cohorts
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.