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Intracortical microelectrode arrays, especially the Utah array, remain the most common choice for obtaining high dimensional recordings of spiking neural activity for brain computer interface and basic neuroscience research.
AFM has high resolution, and does not require the conductivity of samples, so it can be used to characterize PAAs with ultrasmall nanopore arrays, especially the pore diameter less than 20 nm. Figure 2a shows the ultrasmall PAA with the pore diameter of only 4 7 nm and sheet density as high as 2.0 × 1011 cm−2.
Currently, the majority of mammalian expression data in the Gene Expression Omnibus (GEO) are from three-prime arrays, especially the mouse 430 and human u133 series, and these arrays continue to be used in individual labs as well as larger-scale projects, such as the Cancer Genome Atlas [1].
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While we are aware of no such chromosome 4 19 translocations, it remains a distinct possibility that the two inverted chromosome 19q13 SST1 arrays could undergo intra-chromosomal non-allelic homologous recombination inverting the 1 Mb interval between the arrays, especially given the extensive size and >97% sequence identity between the two macrosatellite arrays.
Note that the performance of this algorithm may be influenced by poor quality arrays, especially those with highly scattered and unevenly distributed probe signal intensities.
Such component is almost negligible for a continuous film (not shown), whereas it can be clearly seen for the antidot arrays, especially for the ordered one.
A numerical method is used to describe the angular amplitude and phase responses of non-saturation limited parametric arrays especially within the interaction region of the arrays.
Contrary to previous reports of high turnover [ 8], we found evidence for the maintenance of ancient structural patterns within the arrays, especially within exon 4. The four tandem arrays show different patterns of proliferation and conservation but the weight of evidence points to all four arrays having evolved after the divergence of arthropods from deuterostomes and nematodes.
In previous work, we observed significant unit-to-unit variation in analyte migration distance on large fsPAG arrays, especially in units on the periphery of the device.
An abundant source of candidate SNPs is essential for designing SNP arrays, especially for large genomes like the C. carpio genome.
The use of parasitic arrays and especially the electrically steerable passive array radiator (ESPAR) antennas enables the design of terminals with a single RF front-end and reduced antenna dimensions, i.e., lightweight and compact mobile terminals.
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Justyna Jupowicz-Kozak
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