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In addition, StyI RFLP analysis of the CP amplicon enables the GFLV isolate carried by a single viruliferous X. index to be characterized.
Genome-wide mutational dynamics have been investigated through comparative analysis of the cp genomes of C. oliveri and C. wilsoniana.
However, analysis of the CP sequences from five WANA countries revealed a geographically associated variation among CpCSV isolates.
In silico analysis of the CP sequences of the CpCSV group-I and -II isolates revealed unique restriction sites for each geographic group.
Phylogenetic analysis of the CP nucleotide sequences of 18 samples from the five countries revealed the existence of two geographic groups of CpCSV isolates differing in CP sequences by 8 10%.
The in silico analysis of the CP genomic organization reveals the presence of mariner elements close to the 5′-region in some CP genes like the untranscribed CP (TVAG_218830) [ 25].
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Further analysis of the CP-AFM measurements shows that a strong inversion layer only exists if the valence band offset is large enough, ΔE V > 0.25 eV [13].
Comparative analysis of the CPs in B. dorsalis with those in the model insect Drosophila melanogaster and the closely related Ceratitis capitata, and CPs from mosquitoes, Lepidoptera, Hymenoptera and Coleoptera identified Diptera-specific genes and cuticle development patterns.
Multiplex PCR confirmed serotype classification and serotyped GBS isolates that yielded ambiguous results by the RFLP analysis of the cps gene cluster.
GBS-specific primers (DLTS) were used to identify those isolates that were nontypeable (NT) by RFLP analysis of the cps gene cluster.
The serotypes of the pneumococcal isolates used for comparison of the CST were determined by multiplex PCR analysis of the cps locus as described by Pai et al. [ 26] or by Quellung reaction [ 25].
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