Sentence examples for mean marker density from inspiring English sources

Two hundred and fifty bread wheat lines, mainly Chinese mini core accessions, were assayed for polymorphism and linkage disequilibrium (LD) based on 512 whole-genome microsatellite loci representing a mean marker density of 5.1 cM.

In the present study 512 SSR loci with a mean marker density of 5.1 cM per locus, ranging from 2.2 to 9.4 cM for all 21 chromosomes, were used to measure LD in Chinese wheat genetic resources at both the genome and chromosome levels (Tables 6 9, Figures. 5 and 6).

This resulted in a mean marker density of 1138 markers per chromosome, covering approximately 32.8 kbp/marker.

The previous mean marker density is 1.28 cM per marker, and 3,379 markers were aligned to the assembled scaffolds.

Assuming ∼740 Mb genome size of chickpea, the 834 marker-based genetic linkage map had mean marker density of one marker per 887.3 kb.

Eight molecular marker melon maps were integrated into a single map containing 1592 markers, with a mean marker density of 0.72 cM/marker, increasing dramatically the density over previously published maps in melon.

The average marker density was 5.6 SNP markers per cM or 3.3 SNP markers per recombination point.

The average marker density was 3.2 cM.

To estimate average marker densities, markers with the same position were considered as single marker (unique locus) to avoid an overestimation of the marker density.

Recent advances in genotyping capabilities, especially in crops, mean that genetic marker density is no longer the limiting factor for QTL studies in plants.

However, the results obtained in this study for BTA1, BTA27, BTA28 and BTA29 can probably be attributed to a sampling variation since the number of markers, marker density, mean MAF or proportion of MAF did not differ from the other autosomes studied.