Tandem repeats in the long-read sequencing era.
Global genomic diversity for All of Us.
Competition between sites of meiotic recombination in snakes.
The regulatory landscape of chromatin accessibility.
Unveiling the expanding protein universe of life.
Metabolic engineering of plant medicines.
Genome replication in space and time.
Divergence and conservation of the meiotic recombination machinery.
Challenges and best practices in omics benchmarking.
Context-specific functions of chromatin remodellers in development and disease.
Translating genomic advances into biodiversity conservation.
Fitness effects of mutations throughout evolution.
A TRIP to understand gene regulation.
Transcriptional diversity along the intestinal crypt-villi axis.
A whole-genome shotgun approach to human reference genome sequencing.
Inhibitors of bacterial immune systems: discovery, mechanisms and applications.
Interrogating epigenetic mechanisms with chemically customized chromatin.
Real-time single-molecule imaging of transcriptional regulatory networks in living cells.
The transition from genomics to phenomics in personalized population health.
Chromatin loops facilitate co-regulation of paralogues.
Top predator decline has evolutionary as well as ecological effects.
Effects of regulatory variants across pig tissues.
Ancient migration and the modern genome.
Decoding human genetic variation using a synthetic paradigm.
Swapping genes within and beyond our bodies.
Genomics for monitoring and understanding species responses to global climate change.
Inborn errors of immunity: an expanding universe of disease and genetic architecture.
Scrambling the genome in cancer: causes and consequences of complex chromosome rearrangements.
Non-coding RNAs in disease: from mechanisms to therapeutics.
Spatial resolution of host-microbiome interactions.
Efficient computation reveals rare CRISPR-Cas systems.
De novo genes: from non-genic to genic.
Including diverse populations enhances the discovery of type 2 diabetes loci.
More than a decade of genetic research on the Denisovans.
RNA modifications in physiology and disease: towards clinical applications.
Computational methods for analysing multiscale 3D genome organization.
Genomic surveillance for antimicrobial resistance - a One Health perspective.
Weaponized genomics: potential threats to international and human security.
WNT regulator controls stripe patterning.
Mouse genome rewriting with human DNA for disease modelling.
SWI/SNF function compensated by another chromatin remodeller.
Mary Lyon and the birth of X-inactivation research.
The evolutionary tale of lactase persistence in humans.
Principles and methods for transferring polygenic risk scores across global populations.
Genetics of human brain development.
Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans.
Harnessing deep learning for population genetic inference.
Targeted genome-modification tools and their advanced applications in crop breeding.
What tubulin can teach us about gene regulation.
Genome assembly in the telomere-to-telomere era.
02841 서울 성북구 안암로 145 고려대학교 도서관 학술정보큐레이션팀 | E-MAIL libres@korea.ac.kr
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