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The EST and SNP markers were utilized in the framework linkage map genotyped on the same resource family (Kucuktas et al. 2009), whereas the 147 anonymous microsatellites were utilized for construction of a framework linkage map using an intraspecific resource family (Waldbieser et al. 2001).
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Primers for the LTR regions of four barley (Hordeum vulgare L). retrotransposons [25] and three anchored microsatellite primers were utilized.
In this study, genotypes of 32 microsatellite markers were utilized of which 30 were the same as described in Vähä et al. (2007), where the detailed information and their original references are available.
In order to better understand the genomic processes underlying polyploidization, microsatellite and retrotransposon PCR-based molecular marker techniques were utilized to evaluate exclusively genetic rearrangements in triticale.
With both microsatellite and SNPs, any occasion where multiple markers were utilized from the same locus, the markers were given the locus name for mapping purposes.
Individuals from six laboratory colonies were utilized in the preliminary screening of all microsatellite loci.
Four molecular datasets were utilized in this study: (1) SNP genotypes; (2) microsatellite genotypes; (3) SINE element genotypes; and (4) DNA sequences.
Three microsatellite loci specific to Symbiodinium Clade B (i.e., CA6.38, B7Sym34, and B7Sym36; [38]–[39]) were utilized in this study.
Various currently available catfish genome resources were utilized in this study, including the genetic linkage map [ 48], BAC-derived microsatellite markers [ 48], BAC-based physical map [ 53], BAC end sequences [ 45, 54], and draft genome sequences (Unpublished data).
Whole lung lobes were utilized.
Periodic boundary conditions were utilized.
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