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DNA crosslinking experiments were performed by S.B. and M.U., peptide mapping and site-directed mapping experiments were done by S.B., and histone crosslinking experiments by S.P., M.U.
In the current study, glycosylation mapping experiments were performed for nascent chains containing native helical sequences from the VSV-G protein or gp41 TM segments (Supplementary Fig. 1).
Micro-Raman mapping experiments were used in this study for the first time, in order to investigate the structural properties of the SiC film grown on the Si substrate and also on top of the voids.
Raman mapping experiments were achieved with a computer-controlled x,y-stage from a fixed single cell by using a 100× microscope objective (NA 0.95, Olympus) with the 1 μm step.
Fate mapping experiments were performed by crossing AspM-CreERT2 transgenic mice with Rosa26YFP transgenic mice (obtained from Jackson laboratory).
Linkage mapping experiments were conducted with three independent F2 populations derived from B73 and one of three other inbred lines from the maize association population (CML247, CML333, NC350).
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With this purpose, 3D mapping experiments are carried out with both simulated data and real data from a mobile robot equipped with a 3D range sensor.
Additional fine mapping experiments are underway to determine the functional relationship between qTGW6 and GW5 in controlling seed development.
The marker maps for all QTL mapping experiments are included as supplemental File S6.
Overall, the estimated gene orders presented on the original Koornneef map, where common populations were subjected to standard mapping experiments, are remarkably consistent with known physical locations.
One of the major concerns in association mapping experiments is the possible detection of non-functional, spurious associations resulting from population stratification [30].
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