search
  • Country
    Clear
  • Thematic
    Clear
  • Type
  • Compatibility Level
  • Jurisdiction
5,812 Data sources

  • GB
  • NL
  • CH
  • SG
  • DZ
  • Thematic: No

  • University of Groningen institutional repository

    more_vert
  • more_vert
  • This site provides access to the research outputs of the Université dAlger 2. Users may set up RSS feeds to be alerted to new content. The interface is available in English.

    more_vert
  • more_vert
  • A public standards-compliant repository for gel-based proteomics data linked to protein identification published in the literature, and stores a collection of multi-species reference maps, with thousands of identified spots..

    more_vert
  • more_vert
  • more_vert
  • more_vert
  • more_vert
  • The Mitochondrial Disease Sequence Data Resource (MSeqDR) is a centralized genome and phenome bioinformatics resource built by the mitochondrial disease community to facilitate clinical diagnosis and research investigations of individual patient phenotypes, genomes, genes, and variants. It integrates community knowledge from expert‐curated databases with genomic and phenotype data shared by clinicians and researchers.

    more_vert
  • chevron_left
  • 5
  • 6
  • 7
  • 8
  • 9
  • chevron_right
5,812 Data sources
  • University of Groningen institutional repository

    more_vert
  • more_vert
  • This site provides access to the research outputs of the Université dAlger 2. Users may set up RSS feeds to be alerted to new content. The interface is available in English.

    more_vert
  • more_vert
  • A public standards-compliant repository for gel-based proteomics data linked to protein identification published in the literature, and stores a collection of multi-species reference maps, with thousands of identified spots..

    more_vert
  • more_vert
  • more_vert
  • more_vert
  • more_vert
  • The Mitochondrial Disease Sequence Data Resource (MSeqDR) is a centralized genome and phenome bioinformatics resource built by the mitochondrial disease community to facilitate clinical diagnosis and research investigations of individual patient phenotypes, genomes, genes, and variants. It integrates community knowledge from expert‐curated databases with genomic and phenotype data shared by clinicians and researchers.

    more_vert
  • chevron_left
  • 5
  • 6
  • 7
  • 8
  • 9
  • chevron_right