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The protein sequences of seven genes – merlin, mats, crumbs, fat, dachsous, hippo, and yorkie, which have fewest recombination breakpoints, were chosen for phylogenetic analysis.
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Therefore, Using symmetry arguments, Requiring coverage by multiple (≥ 2) inserts, A set of "true" breakpoints were chosen by mapping Illumina reads for individual NA18507 (obtained from the NCBI short read trace archive) to build 36.1 of the human genome.
The breakpoints were chosen according to The European Committee on Antimicrobial Susceptibility Testing (EUCAST) [ 8].
The EUCAST breakpoints were chosen because of more conservative values (17 ).
Secondly, there might be a bias in genes that were chosen for assessment in previous studies, although they were not particularly enriched at the breakpoints where we did observe greater XCI (reviewed in 2).
The third changed locus was chosen for this breakpoint.
To overcome this limitation, these datasets were computed using breakpoint medians, and the assignment yielded the shortest tree was chosen for a full evaluation by GRAPPA.
Their breakpoint was chosen at 4 y which is exactly in the middle of the age interval 2 6 y.
This breakpoint was chosen as distinction between low level of staffing and not low level of staffing.
The two breakpoints of each rearrangement were chosen at random on the same chromosome for inversions, and on two randomly chosen chromosomes, for translocations.
Primers for RT-PCR were chosen based upon published breakpoint sequences.
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