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Because ECD uses an enzymatic reaction to create electrical signals that can be read directly from the array, there is no need for image analysis or for expensive and delicate optical scanning equipment.
Three probes represent ERBB2 on the array; there is one probe specific for ESR1 and one for PGR.
As such operations act locally on the elements of an array, there is no preference for one distribution scheme over another when distributing (vec{x}) among nodes in a cluster.
For the whole-exome capture array there were a total of 11831 overlapping SNPs and for the custom chr12 capture array there were a total of 1435 overlapping SNPs.
For example, on the vaccinia array there are 16,007 vaccinia-specific probes with a GC content of 8, which is more than for any other level of GC content.
In the SNPs used for the array there is hardly any overlap with the SolCAP array and it is strongly recommended to combine both SNP sets and to select a core collection of robust SNPs completely covering the entire tomato genome.
For droplets inside the array there are significant differences in droplet drag, heat transfer, and mass transfer, and the results depend on the droplet array configuration.
This means that for each gene represented on the array, there are between 160 and 240 measurements of expression level.
For the vaccinia array, there were 16,007 probes with a GC content of 8, more than for any other probe set.
For an m-dimensional array, there are m! orderings of the indices.
For example, on Affymetrix exon arrays there are only four probes for each putative exonic region.
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CEO of Professional Science Editing for Scientists @ prosciediting.com