As a consequence, female speakers were less likely to adopt this new variant, even though they welcomed others (e.g., [D]).
However, young Chiang speakers nowadays did not consistently use this variant even though it had been a robust realization once, and it is likely to die out soon in the near future, which is consistent with Ang's 洪惟仁 (2003, 2012) predictions.
After correction for multiple testing based on false discovery rate and considering the number of analyzed polymorphisms, significant associations were shown for four variants, even though none of these associations survived a genome-wide correction (P < 5 ∗ 10− 8).
The BFM also discriminates LND from variants, even though it is not a criterion for separating these groups.
Of note, such a sequencing depth was sufficiently high to discover most (99.7%) of the variants even though the exome capture was biased against variant carrying alleles.
The estimate using all the genetic variants is more precise than the estimate using only a subset of variants, even though the additional variants are not associated with calcium at nominally significant levels.
It is important to note that Oryza has the greatest number of intron-exon structure variants even though rice has fewer CAD genes than Populus and apparently less overall chromosomal duplications.
However, we have previously shown that turbidity measurements give an estimate of aggregation, but, due to the different morphologies of the aggregates, the values can substantially differ between different TTR variants, even though the total aggregated protein is the same.
Thus, the association at Otogl could be due the Ser177Leu and Ala833Thr variants, even though they were not predicted to have functional effects, or other unknown polymorphisms that are present on the haplotype containing Ser177Leu, Ala833Thr, and rs29362366.
On further inspection, it appears as if our method preferentially selects the longest causal gene with many causal variants, even though the penalty has been adjusted to penalize longer genes more heavily.
Two polymorphic sites and a three amino-acid deletion in RanGAP2 were found to affect the timing and intensity of the Gpa2-induced hypersensitive response to avirulent GP-RBP-1 variants even though they did not confer any gain of recognition of virulent GP-RBP-1 variants.
