Sentence examples for multiple genomic locations from inspiring English sources

GI7 possesses multiple genomic locations across the various genomes: it is present in both the chromosome and plasmid of C3-41, but is only found in the chromosome of 2297 and LP1-G, and is absent in SSII-1; furthermore, it is present in pBSph but absent in the highly similar plasmid pBSph-2.

Exons that were aligned to multiple genomic locations of their own reference genome at current cutoff were filtered out.

Putative SNPs covered by extremely high read counts are more likely to be non-allelic, i.e. the result of paralogy: although a set of reads may align to a single genomic location according to the genome sequence, they in fact are derived from multiple genomic locations that are misrepresented as a single sequence in the currently available genome sequence.

Another 7% of reads were mapped to multiple genomic locations, possibly due to repetitive regions in the human genome.

Of the >480,000 probes on the methylation chip, we discarded probes with ≥90 % sequence similarity to multiple genomic locations, with sequence variants in the probe binding region (1000 Genomes Project, SNPs with a minor allele frequency ≥2/120), and probes located on sex chromosomes, leaving 392,904 autosomal probes for further analysis.

96% of the tags could be mapped to the human genome (hg18), of which 10.1% were repeats or mapped to multiple genomic locations.

Clusters of largely non-related NBS-LRR genes were located at multiple distinct genomic locations and were commonly found in close proximity to previously mapped defence response (DR) genes.

Interestingly, of all 107,279 smRNAs found to match the soybean genome database, 41,897 (39%) mapped to multiple (11 - 103) genomic locations.

In addition to explaining simple tandem duplications FoSTeS/MMBIR mechanisms can also more readily explain the presence of complex rearrangements and the incorporation of stretches of DNA from multiple different genomic locations such as that observed in the case of the BR1 duplication [ Zhang et al., 2009a].

Short-insert libraries (200 500 bp) have a limited capacity to detect SVs mediated by segmental duplications (or low-copy repeats) that harbour a substantial part of SVs (Sharp et al., 2005; Cooper et al., 2007; Kidd et al., 2008; Conrad et al., 2010a), because reads map to multiple similar genomic locations (Li et al., 2008).

Of the total reads, 81.97% matched either to a unique (36.53%) or to multiple (45.44%) genomic locations (Table  1).> -wrap-foot> *The number of unique mapping reads plus multimapping reads equals the total number of total alignments.