Sentence examples for function of the read from inspiring English sources

Fig. 5 Plot of ln(I) vs. 1/T at low-voltage region (−0.1 to −0.5 V) for the LRS of the three types of reset switching (a c) Fig. 6 Nonlinearity as a function of the read voltage of the three types of reset switching in the LRS.

In other words, σ (t i ) 2 in Equations (7) and (8) are obtained from a polynomial of degree 2 giving a robust variance estimate as a function of the read count.

The variance for the negative binomial distribution is estimated using the approach described in Anders and Huber (2010), i.e. we model the variance as a function of the read count using a smooth function.

Mismatch bases (no-match): when a base in an aligned read does not match the reference base, i.e. the probability of the base in the prb file that matches the reference base is below the baseMin Prb threshold; this base is a candidate SNP. Figure 2 shows the probability of a no-match base to be a true SNP as a function of the read weight as found in two datasets.

We plotted the following statistics as a function of the reads whose 5' end mapped to each position on the x-axis.

G1_M gives 52 X mean coverage (1.6 billion reads) for plasma and 27 X for cellular data.> Figure  1 presents the empirical cumulative distribution function of the total read depth at genomic positions for the 4 datasets.

We also report the neutron-induced background as a function of the read-out threshold, by using a GEANT4 simulation of the nuclear emulsion, showing that it amounts to about 0.06 per year per kilogram, fully compatible with the design of a 10 kg × year exposure.

That was, in part, a function of the reading tours he began to do in the late 1970s, at which he would perform various "routines" from his novels: scabrous, cynical, but most essentially funny, like a kind of literary stand-up with an edge.

In earlier publications [ 24, 25], we developed a robust simulation approach to model traditional capillary transcriptome sequencing, which incorporates distributions of the relative start site of cDNA sequences as a function of cDNA length, the read length distribution, and the transcript abundance distribution.

To assess a possible bias, we plotted the percentage of the genome covered by aligned reads as a function of read depth for raw and corrected reads (black squares and circles in Fig. 4).

The identification rate as a function of read depth is sigmoid: Growth initially starts slowly (i.e. when few reads are sampled, only highly abundant transcripts will be represented), whereas in the next phase the function increases approximately linearly, with an additional 7% of spliceforms gained for each doubling of the read depth.