Exploring biodiversity through museomics. Profiling the total transcriptome of single nuclei in archived samples with snRandom-seq. Indirect recognition of pathogen virulence proteins to activate plant immune receptors. Genetic conflict and its resolution between the sexes. The early days of transcriptome sequencing and functional genomics. Genome-wide association testing beyond SNPs. From computational models of the splicing code to regulatory mechanisms and therapeutic implications. Biobanking with genetics shapes precision medicine and global health. The lives of cells, recorded. Ethical governance for genomic data science in the cloud. Slide-tags enables spatial single-nucleus sequencing. The phenotypic consequences of enhancer evolution. Cohesin and CTCF emerge as building blocks of 3D genome structure. Context-specific regulatory variants in precision medicine and agriculture. Multifunctional histone variants in genome function. Progress in toxicogenomics to protect human health. Genome-scale models in human metabologenomics. A call to action to scale up research and clinical genomic data sharing. The evolution of DNA sequencing with microfluidics. Causal inference for epigenetic ageing. Systemic cell-cell communication in cancer. A brief history of metabolic gradient theory. How the waxing and waning of a mutation determines HIV treatment success. DNA methylation in mammalian development and disease. Chromosomal instability as a driver of cancer progression. Inference and applications of ancestral recombination graphs. Evolution and regulation of animal sex chromosomes. Decoding cell-cell communication using spatial transcriptomics. Tracking protein binding to cis-regulatory elements with PRINT. Intrinsically disordered regions as facilitators of the transcription factor target search. Genomic data sharing: you don't know what you've got (till it's gone). Spatial miRNomics: towards the integration of microRNAs in spatial biology. Integrating ELSI study teams in paediatric genomic research efforts. Spatial metabolomics to unravel cellular metabolism. The hidden diversity of tumours. Cytoplasmic mRNA decay and quality control machineries in eukaryotes. Diversity and consequences of structural variation in the human genome. Epigenetic ageing clocks: statistical methods and emerging computational challenges. Epigenetics and individuality: from concepts to causality across timescales. A phylogenetic approach to comparative genomics. The effects of loss of Y chromosome on male health. Progress in understanding the vertebrate segmentation clock. Beyond the black box with biologically informed neural networks. From genome to drug: the hidden story of diversity. The genesis of paleogenetics. Emerging roles of transcriptional condensates as temporal signal integrators. Leveraging genetics to understand ADAR1-mediated RNA editing in health and disease. SHOX value: the pseudoautosomal gene underlying short stature in Turner syndrome. TACIT and CoTACIT for histone modification profiling in single cells and lineage tracing. The therapeutic potential of circular RNAs