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NGS allows for a massive amount of sequence data to be affordably and quickly obtained.
Still, it remains unclear which approaches will benefit the most from this massive amount of sequence data.
The availability of a massive amount of sequence data stimulated in-depth analyses on the organization of bacterial genomes [ 1- 6].
Since a massive amount of sequence data (including the whole genome sequences) is now available, alternative methods of phylogenetic analysis that make use of these data are possible.
First, we used the massive amount of sequence data produced in our experiment to advance the understanding of the evolutionary patterns and processes occurring in the passerine MHC.
The availability of massive amount of sequence data also stimulated in depth evaluation of the organization of the bacterial chromosome [ 5- 9].
Similar(48)
The ability to generate a massive amount of sequencing and genotyping data is transforming the study of human genetic disorders.
Nonetheless, challenges still exist in learning how to most effectively use the massive amount of sequencing or laboratory findings to promote the understanding of drug mechanisms.
The massive amount of sequencing reads obtained from L. menadoensis liver and testis allowed us to apply stringent filtering criteria, both in the processing of raw sequencing reads and in the filtering of assembled contigs, in order to achieve a final set of high quality transcripts and to overcome the most common pitfalls of NGS assemblies.
We used the massive amount of sequencing data published by the 1000 Genomes Project Consortium to construct the Virtual Chinese Genome Database (VCGDB), a dynamic genome database of the Chinese population based on the whole genome sequencing data of 194 individuals.
Next-generation sequencing methods remove these limitations by providing efficiently massive amounts of sequence data.
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