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Adaptive informatics for multi-factorial and high content biological data

Whereas genomic data are universally machine-readable, data arising from imaging, multiplex biochemistry, flow cytometry and other cell- and tissue-based assays usually reside in loosely organized files of poorly documented provenance. This arises because the relational databases used in genomic res...

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Detalles Bibliográficos
Autores principales: Millard, Bjorn L, Niepel, Mario, Menden, Michael P, Muhlich, Jeremy L, Sorger, Peter K
Formato: Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105758/
https://www.ncbi.nlm.nih.gov/pubmed/21516115
http://dx.doi.org/10.1038/nmeth.1600
Descripción
Sumario:Whereas genomic data are universally machine-readable, data arising from imaging, multiplex biochemistry, flow cytometry and other cell- and tissue-based assays usually reside in loosely organized files of poorly documented provenance. This arises because the relational databases used in genomic research are difficult to adapt to rapidly evolving experimental designs, data formats and analytic algorithms. Here we describe an adaptive approach to managing experimental data based on semantically-typed data hypercubes (SDCubes) that combine Hierarchical Data Format 5 (HDF5) and Extensible Markup Language (XML) file types. We demonstrate the application of SDCube-based storage using ImageRail, a software package for high-throughput microscopy. Experimental design and its day-to-day evolution, not rigid standards, determine how ImageRail data are organized in SDCubes. We apply ImageRail to the collection and analysis of drug dose-response landscapes in human cell lines at the single-cell level.