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The two possible explanations for biological saturation with low fluorescence are that the synthesis of amino allyl labeled RNA for these genes is strongly truncated or that there is less DNA printed on the array for these genes.
Antibody array for these proteins were performed using PathScan RTK Signaling Antibody Array Kit Cell Signaling Technologyy) as manufacturer's recommendation.
It should be emphasized that we chose a whole-genome exome array for these initial studies to provide the proof of principle that our methodology works and to maximize our chances of identifying the largest number of novel exons and splicing events of the Drosophila germline, a tissue that has been noted to have a large diversity of transcript isoforms.
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We show the utility of this array for the sensitive detection of these pathogens from complex substrates like soil, plant tissues and irrigation water, and samples that are collected by tomato growers in their greenhouses.
Table 2 includes data from the CodeLink and Affymetrix arrays for these two strains to allow comparisons.
Thus, the reproducibility of the data from the SGH arrays for these three strains was 99.69%, 99.38%, and 99.79% respectively.
All CNAs detected from the methylation arrays for these 23 ETANTR, 12 EBL, 3 MEPL, and 3 additional histologically unidentified cases are outlined in Table 2.
We used whole genome tiling arrays for these analyses because they offer an unbiased view of transcription at the genome level.
Such high levels of AOH were confirmed by the Illumina array for all these cases (Table 2).
# Set up an array for the weights.
This is a major limitation of the use of these arrays for the study of these genes.
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