Sentence examples for variants were from from inspiring English sources

It is interesting to note that, although 87.5% of the clade 3.1 variants were from Asia and 60% of the clade 3.2 variants were from Europe (Table S1), these clades were found to have similar histories (Fig. 6).

The prokaryotic pGEX-JIP1 1-1277), pGEX-JIP1 (128-282) and pGEX-JIP1 (283-660) and the mammalian expression plasmids pEBG-GST-JIP1 and all its deletion variants were from R. Davis [20].

The identified variants were from EDNRA, ROPN1L, C16orf61 and ZNF577 gene regions.

Fifty-nine variants were from 44 candidate gene studies and three variants were identified through GWAS.

Variants were from release 64 (ftp://ftp.ensembl.org/pub/release-64/variation/gvf/homo_sapiens/) and RefSeq splice sites were based on hg19.

The half-life of the recombinant wild-type pro-TGase at 37 °C reached 34.0 min, and those of the variants were from 24.2 min to 11.5 min.

Although none of these associations survive Bonferroni correction for multiple testing, we noticed that two of these potentially associated variants are from the HVSI region.

While the former T cell stimulatory variants are found in α-gliadins from Gli-D2 and Gli-B2, the glutamine to arginine variants are from Gli-A2 (Table 5, Fig. S2).

It is therefore unlikely that the detected variants are from other copies of the CHK2 gene, since they are not from the highly conserved part of the gene.

The GenBank accession numbers of the nAChR alpha6 subunit genes are as follows: alpha6 cDNAs of B. mori variants are EF127797, EF127798, EF127799; alpha6 cDNAs of T. castaneum variants are from EF127806 to EF127810; alpha6 cDNAs of A. mellifera variants are from EF127800 to EF127805.

Targeted capture efficiency and genomic variants were compared from the DNA derived from the two sources.