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The pigeon marker was validated by screening 69 non-pigeon and 9 pigeon fecal samples.
The new marker was validated in vitro and from field water samples obtained in southwest Bay of Biscay ports (north of Spain).
The Pi9-Pro marker was validated in F2 segregating populations, and the results confirmed that both the Pi2-type and Pi9-type genotypes for Pi9-Pro perfectly co-segregated with the blast resistance phenotype.
A putative sex-linked marker was validated in a different pedigree, confirming the potential of this marker as a screening tool in hop breeding programs.
The KASP marker was validated on an independent wheat association mapping (AM) panel consisting of 376 varieties genotyped with 1621 Diversity Array Technology (DArT) markers (data available at http://www.cerealsdb.uk.net/) and phenotyped for awn presence/absence (Supporting Information, Table S1).
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If this genetic marker is validated for SRLV proviral concentration, it can be used for marker-assisted selection to not only reduce susceptibility but also to lower proviral concentration and severity of disease.
Nineteen LTR sequences were isolated using this new method in tree peony and the applicability of the LTR sequences based markers was validated by further SSAP analysis.
Finally, a set of 11 multiplex panels containing the 30 most informative markers was validated and proposed for B. ruziziensis genetic analysis.
The use of markers was validated in a series of PBMC from healthy donors and cancer patients, as well as in tumor-draining lymph nodes and freshly isolated tumors.
The performance of fluorescent probes utilized for detection of ROS, and various mitochondrial markers was validated (Supplementary Figures S5D and E), using MII oocytes cultured in the presence of inducers of apoptosis or inhibitors of the electron transport chain.
Generally, the markers are validated in fine mapping studies.
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