Sentence examples for mean base pair from inspiring English sources

Nucleotide composition was highly A/T skewed, with mean base pair frequencies for NAD1 and NAD4 of A: 0.46, C: 0.12, G: 0.09, T: 0.33 and A: 0.43, C: 0.15, G: 0.08, T: 0.33, respectively.

Within coding regions, the mean base pair overlap number in the S. cerevisiae genome is approximately constant at all positions 100 bp or more into the gene, and approaches the mean for the RA randomizations.

This reduction in the number of base pairs in the reference structure (24.2 versus 10.9 mean base pairs per alignment for positive and 5'-Mxscarna, respectively) artificially increases SEN calculated neutrality as the potential number of base pairs that may be broken and considered deleterious is small.

Read quality was checked with FASTQC and filtering was performed on the reads with PrinSeq-Lite to ensure a mean base-pair quality of score greater than 20.

Additionally, unlike other endonucleases, the specific DNA targeting of Cas9 was guided by an engineered guide-RNA by means of base-pair complementarity.

They are poorly conserved through the course of evolution, unlike other conserved RNA regulators like micro RNAs, siRNAs, and so forth that function by means of base-pairing mechanisms.

Gene diversity (h) is the probability that two randomly compared haplotypes in the sample are different [22], nucleotide diversity is the probability that two random homologous nucleotides are different [23], and the.pairwise difference (d) is the mean number of base-pair differences between all pairs of haplotypes in the sample.

A distance of one essentially means one base pair difference between the observed structure and the closest point on the boundary of the polytope, which need not be the feature vector of a structure.

The difference in mean telomere base pairs (bp) between the two groups in that study suggested approximately 9 17 years of accelerated biological aging in the stressed, compared to the non-stressed, women [58].

a P-values for comparing means based on two-sample paired Student t-tests; P-values for comparing percentages based on Fisher's exact tests.

We then set the genomic average to zero by subtracting the new mean from each base pair for both intrinsic (i.e. model predictions) predictions and in vivo (i.e. CD4+) data.