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GraphQL is a data query and manipulation language that allows specifying what data is to be retrieved ("declarative data fetching") or modified. A GraphQL server can process a client query using data from separate sources and present the results in a unified graph . [ 2 ]
[37] [38] The project was conducted under the auspices of the Linked Data Benchmark Council (LDBC), starting with the formation of a Graph Query Language task force in late 2015, with the bulk of the work of paper writing occurring in 2017. G-CORE is a composable language which is closed over graphs: graph inputs are processed to create a graph ...
These steps are sufficient to provide general purpose computing and what is typically required to express the common motifs of any graph traversal query. Given that Gremlin is a language, an instruction set, and a virtual machine, it is possible to design another traversal language that compiles to the Gremlin traversal machine (analogous to ...
Weak mutation testing (or weak mutation coverage) requires that only the first and second conditions are satisfied. Strong mutation testing requires that all three conditions are satisfied. Strong mutation is more powerful, since it ensures that the test suite can really catch the problems. Weak mutation is closely related to code coverage ...
Mutation is a genetic operator used to maintain genetic diversity of the chromosomes of a population of an evolutionary algorithm (EA), including genetic algorithms in particular. It is analogous to biological mutation .
Site-directed mutagenesis is used to generate mutations that may produce a rationally designed protein that has improved or special properties (i.e.protein engineering). Investigative tools – specific mutations in DNA allow the function and properties of a DNA sequence or a protein to be investigated in a rational approach. Furthermore ...
Complete framework with user-friendly GUI to analyse NGS data. It integrates a proprietary high quality alignment algorithm and plug-in ability to integrate various public aligner into a framework allowing to import short reads, align them, detect variants, and generate reports. It is made for resequencing projects, namely in a diagnostic setting.
The MADS box is a conserved sequence motif. The genes which contain this motif are called the MADS-box gene family. [1] The MADS box encodes the DNA-binding MADS domain. The MADS domain binds to DNA sequences of high similarity to the motif CC[A/T] 6 GG termed the CArG-box. [2] MADS-domain proteins are generally transcription factors.