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The present study was taken up to explore 16S rRNA gene sequence to develop methods that can be used for preliminary identification and can supplement the existing methods for identification of clinically-relevant isolates of the genus Streptococcus.
The current work considers the possibility to use 16S rRNA sequences for this purpose and is useful for practical applications.Thus the present study aims to explore internal features of 16S rRNA gene for preliminary identification of a species that can supplement the existing methods for identification.
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The first was to evaluate these factors for network-based target identification from proteomics data and to compare this approach with an existing method for identification of important proteins from global proteomics data, differential regulation.
More broadly, we demonstrate that an integrative study design is an efficient alternative to existing methods for the identification of genes involved in complex traits.
We conclude that the identification of context-specific reference genes, combined with existing methods for normalization against multiple controls, is expected to significantly improve the quality and sensitivity of expression quantification experiments, facilitating the correct interpretation of RT-qPCR data.
Although the NarL-DNA interactions have been studied in experiment [ 29- 32], the existing methods for prediction of transcription factor binding sites do not allow for the reliable identification of candidate NarL sites.
As a result the existing methods for finding answers and meaning are well known.
This method supplements the existing methods for tolerance improvement of industrial strains, for example gTME.
First, we theoretically investigated the existing methods for measuring crises.
There are several existing methods for peak detection.
This method provides several advantages over existing methods for quantitative methylation analysis.
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