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- Data Repository China (People's Republic of) Compatibility:Not yet registeredPartners:NGDC, CNCB / BIG, CAS, CAS-MPG Partner Institute for Computational Biology (PICB), Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China Comparative Genomics, Population Genetics, GenotypingNGDC, CNCB / BIG, CAS,CAS-MPG Partner Institute for Computational Biology (PICB), Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China
PGG.Population is a database to aid research on genomic diversity and genetic ancestry of human populations, containing over 7000 genomes, covering more than 350 non-overlapping worldwide populations/groups. It stores information on the genomic diversity of each population, including their genetic affinity, population structure, genetic admixture, ancestral architecture, and evidence of natural selection in their genomes.
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re3data: r3d100012342
GSA is a data repository specialized for archiving raw sequence reads. It supports data generated from a variety of sequencing platforms ranging from Sanger sequencing machines to single-cell sequencing machines and provides data storing and sharing services free of charge for worldwide scientific communities. In addition to raw sequencing data, GSA also accommodates secondary analyzed files in acceptable formats (like BAM, VCF). Its user-friendly web interfaces simplify data entry and submitted data are roughly organized as two parts, viz., Metadata and File, where the former can be further assorted into BioProject, BioSample, Experiment and Run, and the latter contains raw sequence reads.
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As a unicellular eukaryote, the budding yeast Saccharomyces cerevisiae strikes a unique balance between biological complexity and experimental tractability, serving as a long-standing classic model for both basic and applied studies. Recently, S. cerevisiae further emerged as a leading system for studying natural diversity of genome evolution and its associated functional implication at population scales. Having high-quality comparative and functional genomics data is critical for such efforts. Here we exhaustively expanded the Telomere-to-Telomere (T2T) S. cerevisiae reference assembly panel (ScRAP) that we previously constructed for 142 strains to cover high-quality genome assemblies and annotations for 264 S. cerevisiae strains from diverse geographical and ecological niches and also 33 outgroup strains from the other Saccharomyces species described in the genus. We created a dedicated online database, ScRAPdb (https://www.evomicslab.org/db/ScRAPdb/), to host this expanded pangenome collection. On top of the pangenome, ScRAPdb also integrates a population-scale pan-omics atlas (pantranscriptome, panproteome, and panphenome) and rich data exploration toolkits for intuitive genomics analyses. All curated data and downstream analysis results could be easily downloaded from the database. We expect ScRAPdb to become a highly valuable platform for the yeast community and beyond, leading to a pan-omics understanding of the global genetic and phenotypic diversity.
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re3data: r3d100012773
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re3data: r3d100011149
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re3data: r3d100012176
iDog is an integrated resource for domestic dog (Canis lupus familiaris) and wild canids that provides the worldwide dog research community a variety of data services. This includes Genes, Genomes, SNPs, Breed/Disease Traits, Gene Expressions, Single Cell, Dog-Human Homolog Diseases and Literatures. In addition, iDog provides Online tools for performing genomic data visualization and analyses.
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eccDNAdb currently includes 1270 eccDNAs, which were identified in 480 samples (of 42 cancers) after analyzing a total number of 3395 tumor samples (of 57 cancers) including patient tissues, patient-derived xenografts, and cancer cell lines. A total number of 54,901 eccDNA genes were annotated and included in the database as well. With the integration of gene expression, clinical information and chromatin accessibility data, eccDNAdb enables users to easily determine the biological function and clinical relevance of eccDNAs in human cancers.
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- Data Repository China (People's Republic of) Compatibility:Not yet registeredPartners:NGDC, CNCB / BIG, CAS, CAS-MPG Partner Institute for Computational Biology (PICB), Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China Comparative Genomics, Population Genetics, GenotypingNGDC, CNCB / BIG, CAS,CAS-MPG Partner Institute for Computational Biology (PICB), Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China
PGG.Population is a database to aid research on genomic diversity and genetic ancestry of human populations, containing over 7000 genomes, covering more than 350 non-overlapping worldwide populations/groups. It stores information on the genomic diversity of each population, including their genetic affinity, population structure, genetic admixture, ancestral architecture, and evidence of natural selection in their genomes.
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For further information contact us at helpdesk@openaire.eu - Data Repository China (People's Republic of) Compatibility:Not yet registeredPartners:NGDC, CNCB / BIG, CAS Genomics, Nucleic acid sequence, readNGDC, CNCB / BIG, CAS
re3data: r3d100012342
GSA is a data repository specialized for archiving raw sequence reads. It supports data generated from a variety of sequencing platforms ranging from Sanger sequencing machines to single-cell sequencing machines and provides data storing and sharing services free of charge for worldwide scientific communities. In addition to raw sequencing data, GSA also accommodates secondary analyzed files in acceptable formats (like BAM, VCF). Its user-friendly web interfaces simplify data entry and submitted data are roughly organized as two parts, viz., Metadata and File, where the former can be further assorted into BioProject, BioSample, Experiment and Run, and the latter contains raw sequence reads.
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For further information contact us at helpdesk@openaire.eu - Data Repository China (People's Republic of) Compatibility:Not yet registeredPartners:Sun Yat-sen University Functional Genomics, Transcriptomics, ProteomicsSun Yat-sen University
As a unicellular eukaryote, the budding yeast Saccharomyces cerevisiae strikes a unique balance between biological complexity and experimental tractability, serving as a long-standing classic model for both basic and applied studies. Recently, S. cerevisiae further emerged as a leading system for studying natural diversity of genome evolution and its associated functional implication at population scales. Having high-quality comparative and functional genomics data is critical for such efforts. Here we exhaustively expanded the Telomere-to-Telomere (T2T) S. cerevisiae reference assembly panel (ScRAP) that we previously constructed for 142 strains to cover high-quality genome assemblies and annotations for 264 S. cerevisiae strains from diverse geographical and ecological niches and also 33 outgroup strains from the other Saccharomyces species described in the genus. We created a dedicated online database, ScRAPdb (https://www.evomicslab.org/db/ScRAPdb/), to host this expanded pangenome collection. On top of the pangenome, ScRAPdb also integrates a population-scale pan-omics atlas (pantranscriptome, panproteome, and panphenome) and rich data exploration toolkits for intuitive genomics analyses. All curated data and downstream analysis results could be easily downloaded from the database. We expect ScRAPdb to become a highly valuable platform for the yeast community and beyond, leading to a pan-omics understanding of the global genetic and phenotypic diversity.
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re3data: r3d100012773
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iDog is an integrated resource for domestic dog (Canis lupus familiaris) and wild canids that provides the worldwide dog research community a variety of data services. This includes Genes, Genomes, SNPs, Breed/Disease Traits, Gene Expressions, Single Cell, Dog-Human Homolog Diseases and Literatures. In addition, iDog provides Online tools for performing genomic data visualization and analyses.
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eccDNAdb currently includes 1270 eccDNAs, which were identified in 480 samples (of 42 cancers) after analyzing a total number of 3395 tumor samples (of 57 cancers) including patient tissues, patient-derived xenografts, and cancer cell lines. A total number of 54,901 eccDNA genes were annotated and included in the database as well. With the integration of gene expression, clinical information and chromatin accessibility data, eccDNAdb enables users to easily determine the biological function and clinical relevance of eccDNAs in human cancers.
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