While planning the mooring array, we considered that the barotropic tide flow is generally concentrated in the underwater passage between the Saya de Malha and Nazareth banks (Morozov and Fomin 1989).
For the CpG island array we considered positive all the clones that satisfied the described criteria: >2 fold enrichment in the α-p63 samples over the negative antibody -α-flag sampleachn each of the three performed experiments.
In this study, instead of requesting CR BS to be deployed together with antenna arrays, we consider decentralized CR networks, which is formed by distributed CR users in a certain area.
For the promoter arrays, we considered all the spots for which more than 70% of the pixels fluoresced with intensity above the median fluorescence intensity of the background plus two standard deviation and those showing enriched IP/control ratio >2 in all four slides were considered positive.
As well as long microsatellite arrays, we considered low copy number repeats, which have not been studied previously in relation to recombination, including those with only two copies.
To avoid having high local synteny due to proximate tandem array genes, we considered the tandem array genes as one neighboring gene.
Therefore, to further increase the bunch charge and the array quantum efficiency, we consider in the following increasing the emitter density by reducing the emitter array pitch.
Affymetrix Biobank array content: We considered a total of approximately 250,000 SNPs from the Axiom Biobank Genotyping Array, including 86,000 putative exonic SNVs and putative LoF variants.
Aside from the modules noted as being shared with the UK-Biobank, the following categories of variants were included in the design for this component: Affymetrix Biobank array content: We considered a total of approximately 250,000 SNPs from the Axiom Biobank Genotyping Array, including 86,000 putative exonic SNVs and putative LoF variants.
