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Because six of the species analysed lacked gene position information, which was not appropriate for ILP identification, a total of 3,811,360 ILP loci were obtained from the remaining 10 species (Supplementary Table S3).
Combining morphological and molecular identification, a total of 23 species were collected during the inventory.
Through soybean genome blast and online software identification, a total of 23 putative BURP genes were identified.
After isolation and identification, a total of forty-one bacterial isolates of amnion were screened for comparative radiation resistance from 1 to 10 KGy of radiation doses.
Through soybean genome blast and online software identification, a total of 75 soybean expansin genes (Additional file 1) were identified based on expansin nomenclature [ 6].
Following identification, a total of 33 potential publications were further analyzed; of these, 9 studies met all the inclusion criteria (Fig. 1) [ 10, 12– 12].
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The second phase of the campaign [214] focused on three themes, document layout analysis, handwriting recognition and writer identification and a total of seven tasks.
This approach resulted in the identification of a total of 1358 grapevine protein kinases.
The use of an accurate-mass LC-QTOF-MS system permitted the identification of a total of seven transformation products (TPs).
The use of an accurate-mass high resolution LC-Q-TOF-MS system permitted the identification of a total of 13 by-products.
In this study, de novo assembly of the C. cohnii transcriptome from three growth stages (i.e., fast growth, fatty acid accumulation and DHA conversion stages) was conducted, leading to identification of a total of 82,106 unigenes with an N50 of 1822 bp, among which 64.7% were annotated based on sequence similarity to known genes in the database.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com