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Breakpoints for the majority of these pericentric inversions are located in the low-recombinant gene-poor pericentromeric regions.
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By MDA, 2G QFP sequences showed significant association with the 3′ breakpoints of the majority of clinical categories (six of seven), while 5' breakpoints were associated with 2G QFP sequences in two of the categories (Additional file 6: Table S3A,B).
According to CLSI breakpoints 98% and 99% of M. catarrhalis and H. influenzae were susceptible to cefuroxime axetil respectively, while with the adoption of EUCAST breakpoints the majority of the strains (>98%) were categorized as intermediate or resistant.
2G QFP and 3G QFP sequences show significant enrichment with both 5′ and 3′ breakpoints for in the vast majority of tests up to 50 nt (including both motif to b-p and b-p to motif analysis; binomial p-values shown in Additional file 4: Table S2).
For the majority of the study period (Jan 2002-Jun 2010), susceptibility breakpoints were based on the British Society for Antimicrobial Chemotherapy BSACC) guidelines [ 8].
The 3' breakpoint lies within an AluSp repeat but there are no recognizable repeat motifs at the 5' breakpoint implicating a mechanism different to Alu-mediated recombination, responsible for the majority of rearrangements in the BRCA1 gene.
For the majority the cause is unknown.
For the majority, life is hard.
The breakpoints for the mean yield are shown in Fig. 3 above.
We use 25th percentile breakpoints for the formation of the groups.
The genomic breakpoints for the heterozygous deletion were determined.
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