Sentence examples for had sequence coverage from inspiring English sources

More than 95% of the spots had sequence coverage exceeding 25%.

The identified proteins had sequence coverage greater than 15% and Mascot scores greater than 200.

Of the 3,427 SNPs (2,427 unigenes) identified in the Maq-default analysis, 1,619 SNPs were recovered and had sequence coverage of at least 8-fold in both bulks (Additional File 2: Table S1).

In projects that had sequence coverage as low as four and five times, the human time required to close the project was reduced by more than 51%and83%3%, respectively [ 55].

It should be noted however, that this analysis is coverage-limited; hence a given virus could be present in both seasons yet have sequence coverage on separate parts of the genome for each season and therefore not be included in this analysis.

The line mean of each mitochondrial parameter was associated with all segregating sites in the DGRP present in four or more DGRP lines, and having sequence coverage levels greater than two and less than thirty [ 26].

A region of the wMelPop genome corresponding to the genes WD0507 to WD0514 in wMel has sequence coverage approximately three times higher than that of the rest of the genome (fig. 3; supplementary fig. S1, Supplementary Material online).

We also noted that that CRUFTS generally have sequence coverage in fewer species than the known ncRNAs, which reflects that the ncRNAs in the known ncRNA set are well conserved.

We associated the line mean of each sleep parameter with all segregating sites in the DGRP present in four or more DGRP lines, and having sequence coverage levels greater than two and less than thirty [ 20].

Sequencing and SNP discovery based on transcriptome sequencing of water stressed plants increased the likelihood of having sequence coverage in genes relevant to water-stress and identification of allelic differences in these genes between the two alfalfa genotypes evaluated in this study.

The results page therefore includes a graphical interface, designed to help users visualize all of the matching different assembly products identified as putative orthologs of the query gene, and to understand which portions of their gene of interest have sequence coverage in the transcriptomes.