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Table 1 SPRINT algorithm flow Function Partition(DataSet S {S training set} Begin If (all s∈S the same mark) then Return; Foreach a∈A Do calculate column attribute a split S into S1 and S2 using the best split attribute Partition(S1); Partition(S2); End SPRINT Fig. 1 Example of attribution list.
The multi-faceted functional decomposition of G is defined as the problem of simultaneously constructing the atlas of decompositions, and the function partition, such that the following objective function is maximized: The right half of the terms captures the cost function of decomposing G into A; the left half, decomposing D into.
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This system architecture, as the basis for the system design and implementation, support aspects like re-use, function partitioning, scalability and distributed development with well defined system interfaces.
Function partitioning depends on the atlas of decompositions because not every partition of the GO DAG is capable of forming a modular decomposition of functional modules.
Recent evolutionary theories suggest that duplicate genes more commonly survive by function partitioning or subfunctionalization, rather than acquiring new functions [ 30].
Zebrafish CYP paralogs that are co-orthologs of the human CYPs could have distinct functions, as a result of function partitioning (subfunctionalization) or differential regulation (temporal and/or organ differences or differences in induction).
According to the model proposed for the evolution of the Syn-Timp cluster [ 40], the locus containing the ancestral nested genes has undergone gene duplications and losses in vertebrates, followed by function partitioning among the resulting paralogs.
In this case, the ancestral OGC locus seems to have undergone duplication after the split between Protostomia and Deuterostomia, followed by function partitioning among the resulting paralogs (Additional file 4).
It then describes how a platform's architecture can make growing complexity manageable by serving two functions, partitioning innovation tasks and facilitating reintegration of an ecosystem's parts.
The idea that lamin functions partitioned differently in different species is also supported by the fact that not all metazoans express two types of lamins.
The cellular layout of partitioned subnetworks strictly depends on the cellular component branch of GO, but the other two functions, partitioning and coloring, can be driven by any annotation associated with a major gene or protein identifier system.
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