Sentence examples for showed significant alignment from inspiring English sources

Host cells cultured on microgrooved surface showed significant alignment and elongation in the axis parallel to microgrooves.

As described above, 110 and 2 Atlantic salmon genome contigs showed significant alignment to two and three Atlantic salmon linkage groups respectively (Table  5).

Of the 88,751 sequences present in the EST cluster, 219 showed significant alignment (E value <10-5) with sequences of class I and class II elements.

The human MNADK residues from 111 to 318 showed significant alignment with NADH kinase domain (conserved domain database (Marchler-Bauer et al., 2011), CDD ID, PLN02929; E-value, 7.3×10−19) (Fig. 2B), and residues from 119 to 324 showed significant alignment with conserved NAD kinase domain (CDD ID, COG0061; E-value, 8.5×10−13) (Fig. 2C).

A further 17% showed significant alignment to the chicken genome at sites with no current functional gene annotation, and the remaining 23% have not yet been aligned to any putative orthologous genomic region.

In total, 30,643 (41.1% of the GRT) sequences showed significant alignment (Blastx E-value < 1 × 10−15) to 22,780 unique protein sequences in the NCBI non-redundant protein database (NR) [ 50].

First, only one-third of the type 2 peptides showed significant alignments (type 2.138% %, type 2.2 37 % and type 2.3 35 % compared to 99%% of type 1 and type 3 peptides).

Similarly, immune cell lines and male reproductive tissues also show significant alignment p-values, but with lower reliability scores.

A total of 52 sequences from the core secretome did not show significant alignment, at an E value cutoff of 10-20, to proteins of these close actinobacterial relatives.

OlfC gene sequences were considered intact if they 1) begin with a signal sequence, 2) end in a stop codon after the seventh predicted transmembrane domain, 3) show significant alignment to all six stereotypical OlfC exons, and 4) possess no internal frame shifts, significant deletions (excluding those caused by gaps in the genome assembly) or stop codons.

But in polyploid species, the existence of homoeologous sequences makes it difficult to differentiate the allelic SNPs from the homoeologous and also paralogous sequence differences, because multiple sequence reads can align to the same genomic location or an individual sequence read can show significant alignment to multiple genomic locations.