Exact(1)
For that reason a more lenient filter has to be applied in the current study for homozygous SNPs, which can be found in the haploid genes, and a more stringent filter requiring higher depth for heterozygous SNPs.
Similar(59)
In this study, we sequenced regions of the 16S rRNA gene at very high depth for a small number of samples (four), resulting in a majority of the estimated GIT microbial diversity being captured.
In addition, higher depth resolution for heavier elements may be possible by using a Lα/Lβ ratio (as shown for Sn in Fig. 4).
Peak DOC refers to the approximate highest depth of coverage noted for that transcript.
In alternative cases, it may reflect the high depth of sequencing used for these transcriptomes; when this analysis was begun, no other dinoflagellate transcriptomes had been sequenced to similar depth.
However the sds for G3 with higher depth did not approach those for genotype data (shown as 'Chip' in Fig. 2) because increasing depth only increases call rate and co-call rate for an individual or a pair, i.e. the method never uses the full information at a SNP, in contrast to G5 which is effectively using the genotypes when depth is high.
Thus, technological advances that greatly decrease LC separation times or eliminate them entirely while still maintaining a high depth of coverage are crucial for future clinical applications.
The resulting reads had high depth of coverage (> 2000x for each isolate when mapped to the N16961 reference genome using MAQ, a short read alignment tool [ 23]), enabling de novo assembly.
The former generates an image of higher dynamic range (i.e., higher bit depth for each pixel) from multiple images having different exposures.
We considered "high coverage" monkeys to be a set of 17 monkeys, each with >25× average coverage, including the 16 monkeys initially chosen for high-depth sequencing and an additional monkey sequenced at a higher depth than originally planned.
NGS is now developing as the diagnostic methodology of choice across a range of applications, including mutation scanning in targeted gene panels and WES for congenital disorders, as well as high depth analysis for tumour profiling.
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