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These model organisms present with ataxia, 17, 92 which is only additionally observed in a New Zealand Huntaway dog model of MPS IIIA.
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However, RAD data from non-model organisms present additional challenges including a high rate of sequencing errors and data processing errors (i.e., de novo assembly and linkage assignment with a distantly related reference genome).
In addition, the short lifespan of this model organism presents an interesting feature for research on aging.
In a practical sense, working with non-model organisms presents unique challenges.
Each of the model organisms presents unique advantages for the study of RASopathies.
Usually, protein names were used in the protein interactions for presenting proteins, whereas for some interactions, the proteins in different model organisms were presented in different ways, which needed to be normalized for the convenience of the following analysis.
In order to stimulate further functional studies on genetic pathways for internal and environmental regulation of carotene synthesis, modification and degradation, an overview on the situation in the most thoroughly studied model organisms is presented.
Equivalent domain co-occurrence networks for 3 other model organisms are presented in the Supplementary Figure S2.
In this paper, research results reported in the available literature, focused on specific and current investigations concerning model organisms, are presented and discussed.
This article reports on a comprehensive study on resolving the ambiguity in mentions of biomedical named entities with respect to model organisms and presents an array of approaches, with focus on methods utilizing natural language parsers.
We chose Synechocystis sp. PCC 6803 as a model organism to present more details on the enzymes of the L-arginine-degrading pathways and to validate the bioinformatic results by a transcript analysis.
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