The phrase "a next generation methodology" is correct and usable in written English.
It can be used when discussing innovative or advanced approaches to a particular process or field of study.
Example: "Our research team has developed a next generation methodology for data analysis that significantly improves accuracy and efficiency."
Alternatives: "an advanced methodology" or "a cutting-edge approach".
In conclusion, a "next-generation" methodology able to assess embryo competence, improving IVF success rates and reducing the likelihood of multiple pregnancies, is urgently required.
This paper proposes process and models for a next generation AOSE methodology.
This work also demonstrates the successful and efficient application of a next generation sequencing methodology.
This situation is analogous to that of object-oriented methodologies and notations pre-UML, and we argue that the time is ripe to begin the development of a next generation agent-oriented software engineering (AOSE) methodology, leading ultimately towards a unified AOSE methodology.
All these factors would render topology-based approaches to be a next-generation benchmark methodology for pathway-based analysis of both microarrays and GWAS data.
Results: Using a human whole exome enrichment technique, chimpanzee and rhesus macaque samples were captured alongside a human sample and sequenced using standard next-generation methodologies.
Next-generation methodologies that build upon these strategies will bundle together the key components of these methodological advances to provide a powerful tool for quantitative descriptions of the phenotypes of this genetic model organism.
This is particularly important for the rapidly expanding set of genomes, like that of the turkey, that are shotgun sequenced solely by "next-generation" methodologies that tend to give shorter sequence contig and scaffold lengths.
454-Pyrosequencing is a next-generation, high-throughput sequencing methodology based on the sequence by synthesis approach and is useful due to its longer read length compared to read lengths generated by the current Illumina or Ion-torrent platforms: 700 bp compared to 300 and 400 bp, respectively.
Finally, we indicate that performing a larger SLE GWAS and applying a more targeted set of methods, such as the ImmunoChip and next generation sequencing methodology, are important for identifying additional loci and enhancing our understanding of the pathogenesis of SLE.
We demonstrate that our B-cell ALL xenograft panel recapitulates the DNA methylation and gene expression profiles of the primary tumour and will facilitate future genome-wide interrogation of gene expression and DNA methylation using next generation sequencing methodology.
