The phrase "a reported variant" is correct and usable in written English.
It can be used when referring to a variant that has been documented or mentioned in reports or studies.
Example: "The study highlighted a reported variant of the virus that showed increased transmissibility."
Alternatives: "an observed variant" or "a documented variant".
When information changes on a previously reported variant, we generate an "alert".
In addition, 5 (11.9%) of the 42 samples were positive for classical US PEDV instead of a recently reported variant PEDV (7 ) (Table 1).
The findings identify that the same SNP associated with T1D and CeD shows stronger association with RA than a previously reported variant and extend the evidence for overlap between autoimmunity genes.
One intriguing preliminary finding was that a significant portion of reported variants strongly associated with cis-regulation tags these globally conserved haplotype frameworks.
Interestingly, our preliminary analysis suggested that a significant portion of reported variants strongly associated with cis-regulation tagged these globally-conserved haplotype frameworks [9].
Although different authors have reported the existence of CNVs in individuals from different geographical locations [29], [35], [40], [45], experimental validation is lacking for a number of the reported variants.
A minority of papers reported variants to be "partially concordant" (3.1%; 27/867), meaning that while the cryptic site observed was predicted, it was not the most likely splice isoform relative to other expressed cryptic exons.
In these projects, samples were sequenced to a very high mean coverage on different sequencing platforms and the reported variants represent an intersection of technical replicates and independent analysis pipelines.
The gltA sequences (338 bp) from all 4 patient samples were identical to those for previously reported variants from a febrile patient in Thailand (GenBank accession no. GQ200857) and from stray dogs in Thailand (GenBank accession no. FJ946836).
FHH is a genetically heterogeneous disorder comprising three reported variants.
