Sentence examples for for individual reading from inspiring English sources

Exact(2)

The simulations not only accounted fairly well for individual reading patterns but also captured the different dyslexia profiles discussed in the literature (i.e., surface, phonological, mixed, and mild dyslexia).

Previous calibration was conducted using a standard surface provided with the equipment, for individual reading of the specimens, at a distance of 4.0 mm (variable X) and making adjustments on the surface area of the specimens (variable Z).

Similar(58)

One shortcoming of this approach is that it either includes or excludes reads for entire exons, rather than making decisions for individual reads.

Instead, we first systematically searched for paired reads that fully mapped to the genome but not at the expected distance or orientation, followed by searching for individual reads mapping across the predicted fusion junction.

After mapping, the genome of origin for individual reads can be identified based on a comparison between the bases at the homoeo-SNP locus and the respective bases of related diploid species a process we call read categorization.

Significance tests for multiple comparisons of proportions [ 44] indicated that each combination of consensus and H37Rv sequences for individual read data in each mapping stringency setting showed significant difference in the proportion of mapped reads (p < 0.0001), with the proportion always higher using CS as the reference.

Significance tests described above showed that each combination of consensus and H37Rv sequences for individual read data in each mapping stringency setting differed significantly difference in the proportion of mapped reads (p < 0.0001), with the proportion always higher using CS as the reference.

For individuals reading the book, I think the questions are fairly obvious and would not add a great deal to your personal reading of the book.

While this format is useful for individuals reading the medical record, information stored as free-text is difficult to use in decision support systems or automated cross population studies [ 1].

The major concerns have been relatively short read lengths (i.e., as of 2007 an average of 100 200 nt compared to 800 1,000 nt for Sanger sequencing), a lack of a paired end protocol and the accuracy of individual reads for repetitive DNA, particularly in the case of monopolymer repeats [ 12].

Quality control was performed to remove homopolymer-rich sequences and poor-quality portions of individual reads (for details, see Wei et al., 2014).

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