NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge
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Pavel P. Kuksa | Nicholas R. Wheeler | P. Kuksa | O. Valladares | Y. Leung | Zivadin Katanic | Emily Greenfest-Allen | W. Bush | Prabhakaran Gangadharan | Jeffrey Cifello | A. Kuzma | Wan-Ping Lee | Li-San Wang | Christian J Stoeckert | Jeffrey Cifello | Nicholas Wheeler | Gerard D. Schellenberg | Gerard D Schellenberg
[1] 2023 Alzheimer's disease facts and figures , 2023, Alzheimer's & dementia : the journal of the Alzheimer's Association.
[2] P. Kuksa,et al. FILER: a framework for harmonizing and querying large-scale functional genomics knowledge , 2022, NAR genomics and bioinformatics.
[3] Jeremy D. DeBarry,et al. VEuPathDB: the eukaryotic pathogen, vector and host bioinformatics resource center , 2021, Nucleic Acids Res..
[4] Ira M. Hall,et al. High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios , 2021, Cell.
[5] Astrid Gall,et al. Ensembl 2021 , 2020, Nucleic Acids Res..
[6] William S Bush,et al. Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies , 2019, PSB.
[7] Thawfeek M. Varusai,et al. The reactome pathway knowledgebase , 2019, Nucleic Acids Res..
[8] Helen E. Parkinson,et al. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 , 2018, Nucleic Acids Res..
[9] Alan F. Scott,et al. OMIM.org: leveraging knowledge across phenotype–gene relationships , 2018, Nucleic Acids Res..
[10] The Gene Ontology Consortium,et al. The Gene Ontology Resource: 20 years and still GOing strong , 2018, Nucleic Acids Res..
[11] The UniProt Consortium,et al. UniProt: a worldwide hub of protein knowledge , 2018, Nucleic Acids Res..
[12] Gregory M. Cooper,et al. CADD: predicting the deleteriousness of variants throughout the human genome , 2018, Nucleic Acids Res..
[13] Mark Gerstein,et al. GENCODE reference annotation for the human and mouse genomes , 2018, Nucleic Acids Res..
[14] Paul Denny,et al. Genenames.org: the HGNC and VGNC resources in 2019 , 2018, Nucleic Acids Res..
[15] Michael Boehnke,et al. emeraLD: Rapid Linkage Disequilibrium Estimation with Massive Data Sets , 2018, bioRxiv.
[16] William S. Bush,et al. Functional annotation of genomic variants in studies of late-onset Alzheimer’s disease , 2018, Bioinform..
[17] J. Michael Cherry,et al. The Encyclopedia of DNA elements (ENCODE): data portal update , 2017, Nucleic Acids Res..
[18] Brent S. Pedersen,et al. GIGGLE: a search engine for large-scale integrated genome analysis , 2017, Nature Methods.
[19] Daniel M. Childress,et al. NIAGADS: The NIA Genetics of Alzheimer's Disease Data Storage Site , 2016, Alzheimer's & Dementia.
[20] James Y. Zou. Analysis of protein-coding genetic variation in 60,706 humans , 2015, Nature.
[21] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[22] Michael Q. Zhang,et al. Integrative analysis of 111 reference human epigenomes , 2015, Nature.
[23] François Schiettecatte,et al. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders , 2014, Nucleic Acids Res..
[24] T. Meehan,et al. An atlas of active enhancers across human cell types and tissues , 2014, Nature.
[25] Nick C Fox,et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease , 2013, Nature Genetics.
[26] Steve Pettifer,et al. EDAM: an ontology of bioinformatics operations, types of data and identifiers, topics and formats , 2013, Bioinform..
[27] Raymond K. Auerbach,et al. An Integrated Encyclopedia of DNA Elements in the Human Genome , 2012, Nature.
[28] D. G. Clark,et al. Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease , 2011, Nature Genetics.
[29] Michael Boehnke,et al. LocusZoom: regional visualization of genome-wide association scan results , 2010, Bioinform..
[30] W. G. Hill,et al. The Limits of Individual Identification from Sample Allele Frequencies: Theory and Statistical Analysis , 2009, PLoS genetics.
[31] S. Nelson,et al. Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays , 2008, PLoS genetics.
[32] M. Ashburner,et al. The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration , 2007, Nature Biotechnology.
[33] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[34] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[35] OUP accepted manuscript , 2021, Database.
[36] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[37] Susumu Goto,et al. KEGG: Kyoto Encyclopedia of Genes and Genomes , 2000, Nucleic Acids Res..