Microbial ecology and evolution in the genomics era.
vol.27 iss.1 (2026) Ancient DNA insights into diverse pathogens and their hosts.
vol.27 iss.1 (2026) Whole-genome spatial transcriptomic imaging with RAEFISH.
(2026) A genomic and epigenomic view of human centromeres.
(2026) Ancestral diversity in complex disease genetics: from discovery to translation.
(2026) From models to molecules: self-organized and instructed modes of developmental patterning.
(2026) Mapping the disease interactome.
(2026) Proteoform medicine: characterizing and targeting protein forms in human disease.
(2026) Interpretation, extrapolation and perturbation of single cells.
(2026) Let the data speak - single-cell analysis with CellWhisperer.
(2026) Bringing methylation profile scores to early life.
(2026) Regulation of gene expression by alternative polyadenylation in health and disease.
(2026) Monitoring biological effects of somatic cell genome editing.
(2026) Emergence and evolution of protein-coding de novo genes.
(2026) Long non-coding RNAs as orchestrators of dosage compensation.
(2026) Bridging behaviour and genomics for tsetse fly control
(2026) pp.1 High-throughput identification of aptamer–target pairs with SPARK-seq
(2026) pp.1 Making sense of the regulatory genome.
vol.26 iss.10 (2025) Cis-regulatory elements at cellular resolution.
vol.26 iss.10 (2025) Is enhancer-driven gene regulation all wrapped up?
vol.26 iss.10 (2025) Regulatory genomics at biobank scales.
vol.26 iss.10 (2025) Predicting the regulatory genome.
vol.26 iss.10 (2025) Regulatory genome annotation.
vol.26 iss.10 (2025) RNA splicing - a central layer of gene regulation.
vol.26 iss.6 (2025) Exploring biodiversity through museomics.
vol.26 iss.3 (2025) Profiling the total transcriptome of single nuclei in archived samples with snRandom-seq.
vol.26 iss.3 (2025) Indirect recognition of pathogen virulence proteins to activate plant immune receptors.
vol.26 iss.3 (2025) Genetic conflict and its resolution between the sexes.
vol.26 iss.3 (2025) The early days of transcriptome sequencing and functional genomics.
vol.26 iss.3 (2025) Genome-wide association testing beyond SNPs.
vol.26 iss.3 (2025) From computational models of the splicing code to regulatory mechanisms and therapeutic implications.
vol.26 iss.3 (2025) Biobanking with genetics shapes precision medicine and global health.
vol.26 iss.3 (2025) The lives of cells, recorded.
vol.26 iss.3 (2025) Ethical governance for genomic data science in the cloud.
vol.26 iss.2 (2025) Slide-tags enables spatial single-nucleus sequencing.
vol.26 iss.2 (2025) The phenotypic consequences of enhancer evolution.
vol.26 iss.2 (2025) Cohesin and CTCF emerge as building blocks of 3D genome structure.
vol.26 iss.2 (2025) Context-specific regulatory variants in precision medicine and agriculture.
vol.26 iss.2 (2025) Multifunctional histone variants in genome function.
vol.26 iss.2 (2025) Progress in toxicogenomics to protect human health.
vol.26 iss.2 (2025) Genome-scale models in human metabologenomics.
vol.26 iss.2 (2025) A call to action to scale up research and clinical genomic data sharing.
vol.26 iss.2 (2025) The evolution of DNA sequencing with microfluidics.
vol.26 iss.1 (2025) Causal inference for epigenetic ageing.
vol.26 iss.1 (2025) Systemic cell-cell communication in cancer.
vol.26 iss.1 (2025) A brief history of metabolic gradient theory.
vol.26 iss.1 (2025) How the waxing and waning of a mutation determines HIV treatment success.
vol.26 iss.1 (2025) DNA methylation in mammalian development and disease.
vol.26 iss.1 (2025) Chromosomal instability as a driver of cancer progression.
vol.26 iss.1 (2025) Inference and applications of ancestral recombination graphs.
vol.26 iss.1 (2025)
vol.27 iss.1 (2026) Ancient DNA insights into diverse pathogens and their hosts.
vol.27 iss.1 (2026) Whole-genome spatial transcriptomic imaging with RAEFISH.
(2026) A genomic and epigenomic view of human centromeres.
(2026) Ancestral diversity in complex disease genetics: from discovery to translation.
(2026) From models to molecules: self-organized and instructed modes of developmental patterning.
(2026) Mapping the disease interactome.
(2026) Proteoform medicine: characterizing and targeting protein forms in human disease.
(2026) Interpretation, extrapolation and perturbation of single cells.
(2026) Let the data speak - single-cell analysis with CellWhisperer.
(2026) Bringing methylation profile scores to early life.
(2026) Regulation of gene expression by alternative polyadenylation in health and disease.
(2026) Monitoring biological effects of somatic cell genome editing.
(2026) Emergence and evolution of protein-coding de novo genes.
(2026) Long non-coding RNAs as orchestrators of dosage compensation.
(2026) Bridging behaviour and genomics for tsetse fly control
(2026) pp.1 High-throughput identification of aptamer–target pairs with SPARK-seq
(2026) pp.1 Making sense of the regulatory genome.
vol.26 iss.10 (2025) Cis-regulatory elements at cellular resolution.
vol.26 iss.10 (2025) Is enhancer-driven gene regulation all wrapped up?
vol.26 iss.10 (2025) Regulatory genomics at biobank scales.
vol.26 iss.10 (2025) Predicting the regulatory genome.
vol.26 iss.10 (2025) Regulatory genome annotation.
vol.26 iss.10 (2025) RNA splicing - a central layer of gene regulation.
vol.26 iss.6 (2025) Exploring biodiversity through museomics.
vol.26 iss.3 (2025) Profiling the total transcriptome of single nuclei in archived samples with snRandom-seq.
vol.26 iss.3 (2025) Indirect recognition of pathogen virulence proteins to activate plant immune receptors.
vol.26 iss.3 (2025) Genetic conflict and its resolution between the sexes.
vol.26 iss.3 (2025) The early days of transcriptome sequencing and functional genomics.
vol.26 iss.3 (2025) Genome-wide association testing beyond SNPs.
vol.26 iss.3 (2025) From computational models of the splicing code to regulatory mechanisms and therapeutic implications.
vol.26 iss.3 (2025) Biobanking with genetics shapes precision medicine and global health.
vol.26 iss.3 (2025) The lives of cells, recorded.
vol.26 iss.3 (2025) Ethical governance for genomic data science in the cloud.
vol.26 iss.2 (2025) Slide-tags enables spatial single-nucleus sequencing.
vol.26 iss.2 (2025) The phenotypic consequences of enhancer evolution.
vol.26 iss.2 (2025) Cohesin and CTCF emerge as building blocks of 3D genome structure.
vol.26 iss.2 (2025) Context-specific regulatory variants in precision medicine and agriculture.
vol.26 iss.2 (2025) Multifunctional histone variants in genome function.
vol.26 iss.2 (2025) Progress in toxicogenomics to protect human health.
vol.26 iss.2 (2025) Genome-scale models in human metabologenomics.
vol.26 iss.2 (2025) A call to action to scale up research and clinical genomic data sharing.
vol.26 iss.2 (2025) The evolution of DNA sequencing with microfluidics.
vol.26 iss.1 (2025) Causal inference for epigenetic ageing.
vol.26 iss.1 (2025) Systemic cell-cell communication in cancer.
vol.26 iss.1 (2025) A brief history of metabolic gradient theory.
vol.26 iss.1 (2025) How the waxing and waning of a mutation determines HIV treatment success.
vol.26 iss.1 (2025) DNA methylation in mammalian development and disease.
vol.26 iss.1 (2025) Chromosomal instability as a driver of cancer progression.
vol.26 iss.1 (2025) Inference and applications of ancestral recombination graphs.
vol.26 iss.1 (2025)
