Those particles trigger the detectors in the array, enabling researchers to deduce the direction and energy of the original cosmic ray.
The resequencing of the variable sequences on the array was comparatively less efficient than the conserved ones; however, the array enabled efficient primer design for the diverse regions, which were subsequently sequenced by an alternate method.
The array enabled a precise localization of the wild barley introgressions in the elite barley background.
The array enabled simultaneous detection of three major sugars, fructose, glucose, and sucrose, in test samples.
The array enabled us to analyze different tumor metastasis-related genes involved in cell adhesion, cell cycle, cell growth and proliferation, apoptosis, extracellular matrix protein, transcription factors, and regulators.
The use of the array enabled us to locate a total of 2,270 SNPs to the consensus linkage map at a fraction of the time and cost of developing a similar map using other experimental approaches, and to develop the most comprehensive saturated complete linkage map for a Malus mapping progeny to date.
Combination of this information with the target composition of fractionated genomic DNA used for hybrization on the arrays enables us to deduce the base pairings in the probe/target complexes producing a particular probe intensity.
Hybridization of the arrays enables us to select genes with an up- or down-regulated expression in children with asthma.
In addition, the high-density of the arrays enabled CSD analysis of laminar profiles obtained through sequential stimulation along the CA1 pyramidal tree.
The result of this careful design procedure means that regions with the highest priority are covered at exon-level resolution on the arrays, enabling single-exon copy-number variation (CNV) detection in up to 502 prioritized genes of interest.
