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For more on the PGP, check out a feature I wrote earlier this year on the challenges of interpreting the huge amount of genomic information made possible by new sequencing technologies.
These data are accumulated by new sequencing technologies and enable his group to learn algorithms to predict disease phenotypes, progression and treatment response for individuals.
Sequence repeats severely hamper the assembly of most genomes, and these repeats continue to obscure genome structure even with the high read depths afforded by new sequencing technologies.
The numerous classes of repeats often impede the assembly of genome sequences from the short reads provided by new sequencing technologies.
With the huge amount of sequence data that are produced by new sequencing technologies, faster methods for sequence comparison are required.
Nevertheless, detailed, manual curation of genes that have published data would greatly assist in computational-based propagation of function to genes identified by new sequencing technologies.
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The data being generated by new sequencing technology extend well beyond human genomic DNA.
This need grows ever more urgent as mountains of data generated by new sequencing technology begin to accumulate, and as we move into the era of personal genome sequencing.
Nevertheless, the huge amount of genomic data produced by the new sequencing technologies prevents this practice.
However, the reliability of the quantification of the methylation level of individual CpG sites by these new sequencing technologies has not been explored comprehensively.
With the increasing interest in the population genomics of D. melanogaster generated by the new sequencing technologies, any new method to genetically isolate completely homozygous or haploid genomes will have great utility.
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by automated sequencing technologies
by new consumer technologies
by parallel sequencing technologies
by other sequencing technologies
by 'NextGen' sequencing technologies
by improved sequencing technologies
by current sequencing technologies
by deep sequencing technologies
by orthogonal sequencing technologies
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