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YeastRGB: comparing the abundance and localization of yeast proteins across cells and libraries.
Dubreuil, Benjamin; Sass, Ehud; Nadav, Yotam; Heidenreich, Meta; Georgeson, Joseph M; Weill, Uri; Duan, Yuanqiang; Meurer, Matthias; Schuldiner, Maya; Knop, Michael; Levy, Emmanuel D.
Afiliación
  • Dubreuil B; Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Sass E; Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Nadav Y; Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Heidenreich M; Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Georgeson JM; Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Weill U; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
  • Duan Y; Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Meurer M; Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Schuldiner M; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
  • Knop M; Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Levy ED; Cell Morphogenesis and Signal Transduction, DKFZ-ZMBH Alliance and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Nucleic Acids Res ; 47(D1): D1245-D1249, 2019 01 08.
Article en En | MEDLINE | ID: mdl-30357397
The ability to measure the abundance and visualize the localization of proteins across the yeast proteome has stimulated hypotheses on gene function and fueled discoveries. While the classic C' tagged GFP yeast library has been the only resource for over a decade, the recent development of the SWAT technology has led to the creation of multiple novel yeast libraries where new-generation fluorescent reporters are fused at the N' and C' of open reading frames. Efficient access to these data requires a user interface to visualize and compare protein abundance, localization and co-localization across cells, strains, and libraries. YeastRGB (www.yeastRGB.org) was designed to address such a need, through a user-friendly interface that maximizes informative content. It employs a compact display where cells are cropped and tiled together into a 'cell-grid.' This representation enables viewing dozens of cells for a particular strain within a display unit, and up to 30 display units can be arrayed on a standard high-definition screen. Additionally, the display unit allows users to control zoom-level and overlay of images acquired using different color channels. Thus, YeastRGB makes comparing abundance and localization efficient, across thousands of cells from different strains and libraries.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Biblioteca de Genes / Biología Computacional / Proteoma / Proteínas de Saccharomyces cerevisiae / Bases de Datos de Proteínas Idioma: En Revista: Nucleic Acids Res Año: 2019 Tipo del documento: Article País de afiliación: Israel Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Biblioteca de Genes / Biología Computacional / Proteoma / Proteínas de Saccharomyces cerevisiae / Bases de Datos de Proteínas Idioma: En Revista: Nucleic Acids Res Año: 2019 Tipo del documento: Article País de afiliación: Israel Pais de publicación: Reino Unido