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The whole-genome sequence should be invaluable reference information to develop more rational and effective methods for identification, genetic stability, and microbial agents in pharmaceutical cell banks.
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In this paper, an effective method for identification of piecewise affine system is proposed.
The high-throughput SNP discovery pipeline presented here is a rapid and effective method for identification of polymorphic SNP alleles in the oat genome.
Because C. sativus is a triploid, we employed in silico screening of a large stigma cDNA EST database [ 43] as an effective method for identification of potential CsGT45 alleles.
The SNP discovery and validation pipeline presented in this study has been shown to be an effective method for identification of SNP markers in oat, a species with a complex and poorly-characterized genome.
While quantitative trait locus (QTL) analysis is an effective method for identification of DNA markers linked to agronomically important traits, few QTL studies have been conducted due to the lack of high-density linkage maps in peanut [ 25, 28, 30, 31].
Thus, high-throughput and cost-effective methods for identification of the mutation status are required.
It is of key importance to apply effective methods for the identification (extraction) of properties from noisy signals.
Effective methods for the identification and enumeration of lactic acid producing bacteria (LAB) cells are important for the quality control and assurance of probiotic products.
Therefore accurate, rapid and cost effective methods for the identification of these NTMs and MTB are greatly needed for appropriate TB management.
Sensitive and effective methods for detection and identification of Ichthyobodo spp. are needed to aid diagnosis of ichthyobodosis and epizootiological studies on Ichthyobodo spp. We have designed a specific quantitative real-time PCR assay targeting SSU rDNA for the detection of Ichthyobodo spp. infections.
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