里程碑式研究:UK Biobank全基因组测序项目揭示人类遗传多样性 在2023年12月13日举办的UK Biobank 2023科学会议上,有一篇发表在医学类论文预印本网站medRxiv的论文Whole-genome sequencing of half-a-million UK Biobank participants引发了学术界...
http://t.cn/A6jM7Zpa 在2023年12月13日举办的UK Biobank 2023科学会议上,有一篇发表在医学类论文预印本网站medRxiv的论文Whole-genome sequencing of half-a-million UK Biobank participants引发了学术界的广...
里程碑式研究:UK Biobank全基因组测序项目揭示人类遗传多样性 在2023年12月13日举办的UK Biobank 2023科学会议上,有一篇发表在医学类论文预印本网站medRxiv的论文Whole-genome sequencing of half-a-million UK Biobank participants引发了学术界的广泛关注。 该研究对约50万人,包括了5个人种的参与者进行了全基因组...
Thousands of missing variants in the UK Biobank are recoverable by genome realignmentDNAexomegeneticssequence alignmentsequence analysisThe UK Biobank is an unprecedented resource for human disease research. In March 2019, 49,997 exomes were made publicly available to investigators. Here we note that ...
Scope:This notebook explains how to explore phenotypic data table and retrieve fields. We will dive deeper into the phenotypic data stored in the Spark database. We will retrieve the information about the fields, and learn how to get a field id, title, and link to the UK Biobank Showcase...
Participation bias in the UK Biobank distorts genetic associations and downstream analyses Article Open access 27 April 2023 Ancestral genetic components are consistently associated with the complex trait landscape in European biobanks Article Open access 10 August 2024 Within-sibship genome-wide as...
Genome-wide association studies of brain structure and function in the UK Biobank The genetic basis of brain structure and function is largely unknown. We carried out genome-wide association studies of 3,144 distinct functional and structural brain imaging derived phenotypes in UK Biobank (discovery ...
Osteoarthritis is a common complex disease imposing a large public-health burden. Here, we performed a genome-wide association study for osteoarthritis, using data across 16.5 million variants from the UK Biobank resource. After performing replication and meta-analysis in up to 30,727 cases and 297...
Illumina Platinum Genomes Menschliche Referenzgenome ClinVar Annotations SnpEff gnomAD 1000 Genomes OpenCravat CODIEREN GATK-Ressourcenpaket TCGA Open Data Pan UK-Biobank Arbeit und Wirtschaft Bevölkerung und Sicherheit Allgemeine Datasets Beispiele Verweis Ressourcen PDF herunterladen Learn...
(I'm pretty sure at the time Hail 0.2 hadn't implemented it's analogous locus type associated with genome build, though I haven't gone back to confirm.) Thescript creating variants.tsv.bgzwas part of the primary Hail 0.1 pipeline and so matches that location-based sort used by all of ...