Sentence examples for repeat position from inspiring English sources
In living cells, we observed examples for three different states of lacO repeat position: "out" (Figure 6A), "edge" (Figure 6B) or "in" (Figure 6C) the chromosome territory.
The distance from the flanking SNPs to the next copy of DEFA1 in repeat position 1 (chr8:6841698–6844134) is 26kb.
As known from orthologs in other plant species, the first conserved tryptophan residue in the R3 repeat (position 60, W) could be replaced by F or less frequently by isoleucine (I), leucine (L) or tyrosine (Y).
That repeats are more similar within species than between species regardless of intragenic repeat position can be explained by rapid intra-specific spread of genetic variation via unequal crossing over during recombination [ 22, 23].
Alternatively, Aldred and colleagues demonstrated that DEFA3 has arisen at the 5' end repeat position and has transferred to other positions within the array through unequal recombination between alleles [ 12], suggesting that recombination has been active in shaping diversity in the DEFA1A3 locus.
In yeast, it is known that nucleosome position is inversely correlated with tandem repeat positions with nucleosome depletion being especially pronounced around AT-rich repeats [ 5].
All DMGs were mapped from the input file PGSC_DM_v3.4_gene.gff, and all repeat positions were mapped from the file PGSC0003DMB.repeatmasker.gff (both provided by the PGSC), to the pseudomolecules.
Those positions that interact are situated mainly on the N-terminal part of each repeat (positions 18 and 19 on the repeat) since the C terminal parts of the repeats are not in contact with the EGFP surface.
Emulsion haplotype fusion systems were designed to link flanking regions to the first gene in the centromeric (shown on the right) and telomeric (shown on the left) repeat positions of the CNV region.
To answer this, allele-specific sequence data from two emulsion fusion PCR systems, one telomeric to the CNV and the other centromeric to the CNV were used to define which gene and associated variants resided in the end repeat positions.
