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It should be noted this approach cannot identify small indels.
This approach cannot identify large insertions in the new genome either.
However, this approach cannot identify genes that have a minor contribution individually but act synergistically when located in the same CNV regions.
Second, our genetic labeling approach cannot identify the identity of the parent cell (prior to activation of the αMHC promoter) that gives rise to endogenous committed cardioblasts.
However, recent reports have indicated that this approach cannot identify the newly described Salmonella Typhi isolates that are Nal susceptible (NalS CipDS for which mechanisms of resistance are not linked to mutations in gyrA (7, 10, 11 ).
However, this approach cannot identify RD facets, because it does not reveal whether a facet occupies a unique part of the construct variance not already covered by one or more of the other facets.
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However, this approach alone cannot identify improvement opportunities regarding systemic factors of human errors in RHIS.
The constraints we have imposed through our strategy would necessarily underestimate the number of varietal SNPs between genotypes because our approach i) cannot identify varietal SNPs located in regions unique to either the At or Dt genome, as our SNP calling relies on the presence of both At and Dt reads; and ii) will miss the genuine varietal SNPs without a flanking subgenome-specific SNP.
In the former case, since the mRNA expression of the targets does not any change, transcriptomics approach, such as expression array, cannot identify the targets.
Persons with access to the data cannot identify or attempt to identify individuals in the database.
Further, although this approach may reveal many ET facets, it cannot identify them reliably.
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