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Moreover, after QTL mapping, the molecular markers corresponding to QTLs will be adopted for marker-assisted selection (MAS) for interested agronomic traits.
However, our understanding about how these parallel pathways develop is still in its infancy, because few molecular markers corresponding to individual RGC types are available.
Then, we studied the expression of molecular markers corresponding to the extrinsic and intrinsic apoptotic pathways, in addition to markers of the unfolded protein response (UPR).
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One can efficiently map molecular markers to corresponding BACs via multiplex macroarray hybridization techniques or by using multiplex PCR strategies [ 28- 30].
A calibration of these parameters with extensive experimental data and with the corresponding molecular markers may be important for identifying the main effect of these cellular processes on the bacteria-neutrophil population dynamics in health and in disease.
Two corresponding molecular markers (Pina-N1 and Pina-N2), which span the deletions, were developed for straightforward identification of the Pina-D1b and Pina-D1r alleles.
The analysis of disease resistance QTL locations in the soybean genome using data on corresponding molecular markers (http://soybase.org/) confirmed a strong bond between these sites and the Hsp20 genes.
Two novel alleles Pina-D1s and Pina-D1u at the Pina-D1 locus were characterized at the DNA level by a primer walking strategy, and corresponding molecular markers were developed for straightforward identification of these two alleles.
Two novel Pina-D1 alleles, designated Pina-D1s with a 4,422-bp 4,422-bp andeletion1u with and,460-bp deletion in the Ha (Hardness) locus, were characterized at the DNA level by a primer walking strategy, and corresponding molecular markers Pina-N3 and Pina-N4 with developed for straightforward identification of the Pina-D1s and Pina-D1u alleles.
However, such maps are rare because it is difficult to develop both wild pedigrees and corresponding sets of molecular markers that are sufficiently large.
Because of the many reports of genes/QTL in the soybean genome positioned using SSR or SNP markers, the corresponding physical position of the molecular markers in the new assembly vs. the older assembly is frequently requested by users.
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