Sentence examples for different deletions from inspiring English sources

a The variation sites where the different deletions occur; "∇" indicates the deletions.

A BD AccuriTM C6 (Becton-Dickinson, NJ, USA) was used for the evaluation of the redox biosensor in the different deletions strains.

For example, the four genotypes from Senegal were no more similar to each other than to the genotypes from North America; nevertheless the genotypes with similar deletion patterns have more shared SNPs than genotypes with different deletions (Fig. 3).

One encoded the predicted full length leptin binding domain while the other cDNAs were shorter as a consequence of different deletions in exon 9, and one had a further deletion in exon 10.

We identified 17 individuals with exon-disruptive CNVs (18.5%), including 13 different deletions in eight BBS genes (BBS1, BBS2, ARL6/BBS3, BBS4, BBS5, BBS7, BBS9, and NPHP1) and a deletion and a duplication in other ciliopathy-associated genes (ALMS1 and NPHP4, respectively).

First, different people have different deletions.

To thoroughly investigate quantitative differences in GUS expression among lines carrying different deletion:reporter constructs, we determined the relative amount of GUS transcript by quantitative RT-PCR (qRT-PCR).

The fact that groups B, C, D and E have varying level of deletions suggest each went through different deletion events.

Despite the presence of partial gene clusters in groups B, C, D and E each group has remnants of different deletion events as indicated by the sequenced ends (Fig. 2).

Through molecular modeling and comparative analysis of machines assembled with protein-tagged components or from different deletion mutants, we determined the molecular architecture of the secretion machine in situ and localized its structural components.

The current work suggests deletion of aflatoxin-biosynthesis genes is an ongoing process with genotypes retaining both varying percentages of the aflatoxin cluster and multiple genetic defects sufficient to cause non-aflatoxigenicity. Shared deletion patterns (Table 2; Fig. 2) suggest different deletion events lead to non-aflatoxigenicity in founding genotypes for the various lineages.