Sentence examples for wide variants from inspiring English sources

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To identify genome wide variants, sequences of each species were trimmed using Flexbar [ 25] and were aligned to the reference assembly from which they were derived using BWA-mem [ 26].

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The properties such as porosity, presence of alkaline and earth alkaline metallic cations in zeolites structure along with high mechanical and chemical resistance provide good adsorptive, cation exchange, and catalytic characteristics and make them desirable for wide variant of analytical purposes [50, 51].

The empirical Ti/Tv ratios are ~2.0 for genome-wide variants and ~3.0 3.3 for coding variants [ 18, 27].

As the ability of this work to validate many of the variants associated with menopausal age, as well as discover new genome-wide variants associated with follicle number is limited by sample size, future studies may aim for validation of these findings.

In contrast to the cattle strains isolated from farms associated with human infections, as described above, analyses of VTEC O157 H7 isolated from cattle sampled at slaughter showed a wide variation in variants.

Twain broke with the tradition of asking "Who Am I?" and its species-wide variant "Who Is Man?" on the grounds that a "who-question" is a leading question.

Tools for genome-wide variant identification can be grouped into four categories: (i) germline callers, (ii) somatic callers, (iii) CNV identification and (iv) SV identification.

The same massively parallel sequencers are simultaneously being used for whole-genome resequencing and comprehensive, genome-wide variant discovery in studies of somatic diseases such as cancer.

Figure 8 shows that breakpoint intervals were significantly longer than the average spacing between variants (median 106 bp, compared with 15 bp for genome-wide variant spacing; K-S test: D = 0.50, p-value << 0.001).

The germline mutation rate was extrapolated from the frequency of experimentally validated germline mutations relative to the total number of potential germline mutations from the genome-wide variant calls.

NGS technologies offer the advantage of unbiased genome-wide variant detection in small nuclear families and sporadic cases that previously could not be used effectively with traditional linkage analysis.

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