Sentence examples for by dividing the sequence from inspiring English sources

Hence, to describe the effect brought by the length of protein sequence, the sequence length feature is used and normalized by dividing the sequence length by 1000.

In transcripts, we also obtained the maximum TE by dividing the sequence in 90 nucleotide windows and selecting the window with the highest TE value.

Flanking regions of 5 kb are extracted for all hits with e value < 1e− and direct repeats greater than 200 bases are searched by dividing the sequence in two and using BLASTN alignment.

Fortunately, the sequence, protein architecture and intron positions of tetraspanins are highly conserved within ortholog lineages (in practice, we can divide tetraspanins in 4 TM, 2EC, and the large EC can be further divided into 4-6 portionso so by dividing the sequence into these short portions it is easy to detect and correct the sequence problem.

The false discovery rate for this dataset, estimated at <1%, was calculated by dividing the sequence-reversed proteins that failed to be eliminated after applying the above criteria.

Then, the estimated genome size was obtained by dividing the total sequence length by the real sequencing depth.

TopHat performs an alignment to the genome by dividing the cDNA sequence, and when it matches the genome, TopHat presumes that place to be a splice junction.

RS and RN values for each branch were calculated by dividing the mitochondrial sequence divergences from the combined data set by the elapsed time along that branch (Table 1).

We used an overall estimate of r = 1.4 × 10-9 that we obtained by dividing the autosomal sequence divergence between chicken and turkey (0.1008) from Axelsson et al. [ 60] with the time of divergence between chicken and turkey of 28 × 106 – 45 × 10[ 62] 62].

We simulated experimental choices of n-controls vs. n-treatments biological replicates at n = 2, 3, 4, 6, 8 and 12. Multiplexing various samples into one sequencing lane reduces the monetary cost of RNA-Seq DE analysis, albeit by dividing the available sequencing depth over various samples.

Instead, error probabilities are directly calculated by dividing the observed sequencing errors by total number of observations defined by the joint variables.