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The resulting mtDNA sequences increases the number of sequenced mitochondria in the Danish population more than 10-fold and give a precise picture of the genetic variation segregating, both in terms of haplogroup frequencies and in terms of new and rare variation.
Using the RP set of sequences increases the speed of similarity searches, and aids in the identification of homologs, protein family classification, and comparative genomic and proteomic analyses.
The results of these studies [12], [13] suggest that the social affordances guiding approaching action sequences increases the accuracy demand during the execution of these sequences.
The presence of isomer sequences increases the complexity of the functional roles of these regulatory molecules, but information as provided in this study about precisely the number and identity of the isomiR sequences is requisite for detailed decoding of the miRNAome.
However, adding sequences increases the chance of a new sequence bridging two previously separate OTUs.
Thus, the saturation of the taxonomic space by complete genome sequences increases the opportunities for the application of comparative genomics.
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The inclusion of gap sequences increased the total size of the assembly from 10.45 Gb to 10.46 Gb.
Therefore, multiple target KSHV sequences increase the detection efficiency, while nested PCR protocols are likely to introduce false positivity.
In large studies over the past decade, scientists found that minor changes in human DNA sequences increase the risk that a person will get those diseases.
Using region-specific template sequences increased the search speed by up to 56%.
Increasing the reference genome by adding publicly available turkey BAC-end sequences increased the number of SNPs to over 11,000.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com