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Eight markers could not be assigned to a barley linkage group.
Close et al. [ 11] used MergeMap to integrate four barley linkage maps genotyped at nearly 3000 SNP markers.
The ESTs were derived from non-redundant 3' sequences, generating a comprehensive distribution of genes on the barley linkage map.
In a second step SNP marker were developed for as many as possible of those genes and used to anchor them on the barley linkage map.
When applied to four barley linkage maps genotyped at nearly 3000 SNP markers, DAGGER produced a consensus map with improved fine structure compared to the existing barley consensus SNP map.
The identified QTL explained 29.9% of the total variation [ 44], and the authors deduced that this QTL was located on chromosome 1H based on the published barley linkage maps [ 45].
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Table 2 shows that this information comes from the Oregon Wolfe Barley (OWB) linkage map, and that no other ordinal information for the hardness locus markers is present in the linkage maps.
The expression patterns of drought regulated genes were monitored during plant ontogeny, mapped and the location of these genes was incorporated into a comprehensive barley SNP linkage map.
However, from this comparison of the edited positions in rice versions 5 versus 6 to the 2943 SNP barley genetic linkage map, it appears that the barley SNP map is the more stable point of reference.
This study investigates the plasma metabolic effectiveness from 3.3 g mixed linkage barley or oat β-glucan fibre per day by 1H NMR spectroscopy on plasma samples and multivariate data analysis.
In barley, a RAD linkage map was recently produced in a double haploid population and used for QTL analysis [ 12].
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