Sentence examples for mean depth per from inspiring English sources

Sequencing was conducted at a mean depth per sample of 8.9 × 10 paired-end reads of 100 nt (range 7.6 10.3 × 10 reads).

In the targeted capture data, mean depth per individual at the 6575 targeted sites was 120x (median depth per individual = 102x; minimum individual depth = 35x; Figure 1, Figure S1).

Minimum and maximum depths were set to five and twice the average depth per sample, respectively.

Table 4 shows the surveyed EGRs arranged by ordinal age groupings of mean depth (mm) per roof.

For this subset, mean depth of coverage per site per individual was 8.3×.

The genomes of these individuals were profiled by the use of high-throughput short read sequencing, with ~9X mean depth of coverage per line and compared with the Southern Japanese reference HdrR sequence.

We obtained two new xenopus frogs (Xenopus borealis and X. victorianus) complete mitochondrial genome sequences by means of long-PCR followed by 454 of individual genomes (approach 1) or of multiple pooled genomes (approach 2), the mean depth of coverage per nucleotide was 9823 and 186, respectively.

The raw Illumina sequencing data was aligned to the H37Rv reference genome using the Burrows-Wheeler Alignment Tool v.0.6.1, yielding high coverage data for all isolates (mean read depth per position, mean 249.9, range 44 1411 fold; mean 99.1% genome covered, range 98.6 - 99.9%) (Table  1) [ 82].

Following alignment, processing and duplicate removal, a mean depth of 40.12 reads per base was observed in the shared homozygous regions, with 95.5% of coding bases covered by at least 5 reads.

On an average, 12 Gb of sequencing data were generated from each individual, resulting in a mean depth of more than 110 × per base per targeted region.

Mean depth of coverage was calculated per base pair for all samples; however, only the results of subjects having RP1 mutations were shown.