dbSNP: the NCBI database of genetic variation

• Genomic data in the All of Us Research Program · 2024

• Aberrant phase separation and nucleolar dysfunction in rare genetic diseases · 2023

• jMorp: Japanese Multi-Omics Reference Panel update report 2023 · 2023

• The UCSC Genome Browser database: 2024 update · 2023

• PeSTo: parameter-free geometric deep learning for accurate prediction of protein binding interfaces · 2023

• Neoadjuvant therapy with immune checkpoint blockade, antiangiogenesis, and chemotherapy for locally advanced gastric cancer · 2023

• Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes · 2022

• Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project · 2022

• The co-evolution of the genome and epigenome in colorectal cancer · 2022

• The UCSC Genome Browser database: 2023 update · 2022

• Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis · 2022

• Predicting dynamic cellular protein–RNA interactions by deep learning using in vivo RNA structures · 2021

• The variant call format provides efficient and robust storage of GWAS summary statistics · 2021

• Ensembl 2022 · 2021

• Ensembl 2021 · 2020

• RMVar: an updated database of functional variants involved in RNA modifications · 2020

• Dating genomic variants and shared ancestry in population-scale sequencing data · 2020

• The UCSC Genome Browser database: 2021 update · 2020

• Broad host range of SARS-CoV-2 predicted by comparative and structural analysis of ACE2 in vertebrates · 2020

• Therapy-Induced Evolution of Human Lung Cancer Revealed by Single-Cell RNA Sequencing · 2020

and 121 more

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