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- Data Repository Belgium, United States Compatibility:Not yet registeredPartners:UMD, UMD, Quest Diagnostics (United States) Oncology, Genetics, Life ScienceUMD,UMD,Quest Diagnostics (United States)
BRCA Share is a novel gene datashare initiative that provides scientists and commercial laboratory organizations around the world with open access to BRCA Share (formerly UMD-BRCA1) contains BRCA1 and BRCA2 genetic data. The program’s goal is to accelerate research on BRCA gene mutations, particularly variants of uncertain significance, to improve the ability of clinical laboratory diagnostics to predict which individuals are at risk of developing these cancers.
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For further information contact us at helpdesk@openaire.eu - Data Repository Canada, United States Compatibility:Not yet registeredPartners:OCUL, OCUL, York University, IQSS, Dataverse Project +2 partners Humanities and Social Sciences, Humanities, Life SciencesOCUL,OCUL,York University,IQSS,Dataverse Project,Dataverse Project,IQSS
re3data: r3d100012812 , r3d100012812
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:Zdaly, WorldData.AI, Zdaly, WorldData.AI Humanities and Social Sciences, Social Sciences, Political ScienceZdaly,WorldData.AI,Zdaly,WorldData.AI
re3data: r3d100013323 , r3d100013323
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For further information contact us at helpdesk@openaire.eu - Data Repository United Kingdom, United States Compatibility:Not yet registeredPartners:Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK, Harvard Stem Cell Institute, Cambridge, MA, USA, Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK, Harvard Stem Cell Institute, Cambridge, MA, USA Life Science, Expression data, Stem cellOxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK,Harvard Stem Cell Institute, Cambridge, MA, USA,Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK,Harvard Stem Cell Institute, Cambridge, MA, USA
The Stem Cell Commons were initiated by the Harvard Stem Cell Institute to develop a community for stem cell bioinformatics. This open source environment for sharing, processing and analyzing stem cell data brings together stem cell data sets with tools for curation, dissemination and analysis. Standardization of the analytical approaches will enable researchers to directly compare and integrate their results with experiments and disease models in the Commons.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:collected from a compatible aggregatorPartners:Blackfynn Inc., Blackfynn (United States) Neurosciences, Medicine, Life SciencesBlackfynn Inc.,Blackfynn (United States)
re3data: r3d100013148
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:NIH Life Science, Signaling, Molecular interactionNIH
The Pathway Interaction Database is a highly-structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signaling pathways.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States, United Kingdom Compatibility:Not yet registeredPartners:KFF, Google Arts & Cultures, University of South Florida Libraries, OHA, HES +5 partners Humanities and Social Sciences, Ancient Cultures, HistoryKFF,Google Arts & Cultures,University of South Florida Libraries,OHA,HES,Google Arts & Cultures,HES,CyArk,CyArk,University of South Florida Libraries
re3data: r3d100013317 , r3d100013317
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:NCBI, NCBI Epigenetics, Genetics, Biomedical ScienceNCBI,NCBI
re3data: r3d100010788 , r3d100010788
The Database of Genotypes and Phenotypes (dbGaP) archives and distributes the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:UCAR, UCAR Environmental Science, Earth ScienceUCAR,UCAR
A collection of earth science-related data available to the research community.
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re3data: r3d100010905 , r3d100010905
The Trace Archives includes the following archives: The Sequence Read Archive (SRA) stores raw sequence data from "next-generation" sequencing technologies including 454, IonTorrent, Illumina, SOLiD, Helicos and Complete Genomics. In addition to raw sequence data, SRA now stores alignment information in the form of read placements on a reference sequence. The Trace Archive serves as the repository of sequencing data from gel/capillary platforms such as Applied Biosystems ABI 3730®. The Trace Assembly Archive stores pairwise alignment and multiple alignment of sequencing reads, linking basic trace data with finished genomic sequence as found in GenBank.
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- Data Repository Belgium, United States Compatibility:Not yet registeredPartners:UMD, UMD, Quest Diagnostics (United States) Oncology, Genetics, Life ScienceUMD,UMD,Quest Diagnostics (United States)
BRCA Share is a novel gene datashare initiative that provides scientists and commercial laboratory organizations around the world with open access to BRCA Share (formerly UMD-BRCA1) contains BRCA1 and BRCA2 genetic data. The program’s goal is to accelerate research on BRCA gene mutations, particularly variants of uncertain significance, to improve the ability of clinical laboratory diagnostics to predict which individuals are at risk of developing these cancers.
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For further information contact us at helpdesk@openaire.eu - Data Repository Canada, United States Compatibility:Not yet registeredPartners:OCUL, OCUL, York University, IQSS, Dataverse Project +2 partners Humanities and Social Sciences, Humanities, Life SciencesOCUL,OCUL,York University,IQSS,Dataverse Project,Dataverse Project,IQSS
re3data: r3d100012812 , r3d100012812
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:Zdaly, WorldData.AI, Zdaly, WorldData.AI Humanities and Social Sciences, Social Sciences, Political ScienceZdaly,WorldData.AI,Zdaly,WorldData.AI
re3data: r3d100013323 , r3d100013323
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For further information contact us at helpdesk@openaire.eu - Data Repository United Kingdom, United States Compatibility:Not yet registeredPartners:Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK, Harvard Stem Cell Institute, Cambridge, MA, USA, Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK, Harvard Stem Cell Institute, Cambridge, MA, USA Life Science, Expression data, Stem cellOxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK,Harvard Stem Cell Institute, Cambridge, MA, USA,Oxford e-Research Centre, Department of Engineering Science, University of Oxford, Oxford, UK,Harvard Stem Cell Institute, Cambridge, MA, USA
The Stem Cell Commons were initiated by the Harvard Stem Cell Institute to develop a community for stem cell bioinformatics. This open source environment for sharing, processing and analyzing stem cell data brings together stem cell data sets with tools for curation, dissemination and analysis. Standardization of the analytical approaches will enable researchers to directly compare and integrate their results with experiments and disease models in the Commons.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:collected from a compatible aggregatorPartners:Blackfynn Inc., Blackfynn (United States) Neurosciences, Medicine, Life SciencesBlackfynn Inc.,Blackfynn (United States)
re3data: r3d100013148
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:NIH Life Science, Signaling, Molecular interactionNIH
The Pathway Interaction Database is a highly-structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signaling pathways.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States, United Kingdom Compatibility:Not yet registeredPartners:KFF, Google Arts & Cultures, University of South Florida Libraries, OHA, HES +5 partners Humanities and Social Sciences, Ancient Cultures, HistoryKFF,Google Arts & Cultures,University of South Florida Libraries,OHA,HES,Google Arts & Cultures,HES,CyArk,CyArk,University of South Florida Libraries
re3data: r3d100013317 , r3d100013317
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re3data: r3d100010788 , r3d100010788
The Database of Genotypes and Phenotypes (dbGaP) archives and distributes the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
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For further information contact us at helpdesk@openaire.eu - Data Repository United States Compatibility:Not yet registeredPartners:UCAR, UCAR Environmental Science, Earth ScienceUCAR,UCAR
A collection of earth science-related data available to the research community.
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re3data: r3d100010905 , r3d100010905
The Trace Archives includes the following archives: The Sequence Read Archive (SRA) stores raw sequence data from "next-generation" sequencing technologies including 454, IonTorrent, Illumina, SOLiD, Helicos and Complete Genomics. In addition to raw sequence data, SRA now stores alignment information in the form of read placements on a reference sequence. The Trace Archive serves as the repository of sequencing data from gel/capillary platforms such as Applied Biosystems ABI 3730®. The Trace Assembly Archive stores pairwise alignment and multiple alignment of sequencing reads, linking basic trace data with finished genomic sequence as found in GenBank.
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