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Dorothea Emig

Researcher at Max Planck Society

Publications -  12
Citations -  684

Dorothea Emig is an academic researcher from Max Planck Society. The author has contributed to research in topics: Alternative splicing & Protein–protein interaction. The author has an hindex of 8, co-authored 12 publications receiving 623 citations.

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AltAnalyze and DomainGraph: analyzing and visualizing exon expression data

TL;DR: A new software workflow composed of the open-source application AltAnalyze and the Cytoscape plugin DomainGraph provides an intuitive and comprehensive end-to-end solution for the analysis and visualization of alternative splicing data from Affymetrix Exon and Gene Arrays at the level of proteins, domains, microRNA binding sites, molecular interactions and pathways.
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Specificity of Linear Motifs that Bind to a Common Mitogen-Activated Protein Kinase Docking Groove.

TL;DR: A coherent structural model for MAPK docking specificity is suggested that reveals how short linear motifs binding to a common kinase docking groove can mediate diverse interaction patterns and contribute to correct MAPK partner selection in signaling networks.
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Partitioning biological data with transitivity clustering.

TL;DR: The bead-based registration framework is currently the only solution allowing robust, real-time registration of time-lapse SPIM recordings and enables fully unguided registration without prior knowledge of the arrangement of the views, and outperforms intensity- based registration approaches in terms of precision and speed.
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Comprehensive cluster analysis with Transitivity Clustering

TL;DR: This protocol guides the user through the most important features of Transitivity Clustering and takes ∼1 h to complete: protein (super)family detection with Cytoscape, protein homology detection with incomplete gold standards and clusters of gene expression data.
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Tissue-specific proteins and functional implications.

TL;DR: The analysis based on RNA-sequencing suggests that tissue-specific protein interactions are less common and mainly involved with transmembrane transport and receptor activation, and the number of alternative transcripts is increased for widely expressed genes, suggesting that alternative splicing plays a prominent role in generating specific functional characteristics of tissues.