Sentence examples for trimming criterion from inspiring English sources

The proper rupture area of the earthquake was estimated applying the trimming criterion of Somerville et al. (1999) into the derived slip model.

The rupture area of the earthquake was estimated using the trimming criterion of Somerville et al. (1999) with the slip model from the waveform inversion.

We applied the trimming criterion of Somerville et al. (1999) to remove columns of their average slip below 0.3 times the average slip of the entire fault (0.69 m in this study) from our slip model in order to estimate the proper rupture area of the earthquake.

We estimated S of these eight events from the inversion models of previous studies (Yen 2002; Chi and Dreger 2004; Lee et al. 2015) according to the trimming criteria of Somerville et al. (1999).

Reads passing trimming criteria were analyzed using standard RNA-Seq protocols implemented in CLC.

Quality trimming criteria included no mismatch in MID sequences and a maximum of 1 mismatch in primer sequences.

Quality trimming criteria included no mismatch in the bar code sequences and maximally 1 mismatch in the primer sequences.

After applying coverage criteria, trimming all loci to the length of the second shortest sequence and removing all internal gapped characters, the mean locus length was 534 bp with a minimum and maximum lengths of 250 bp and 1458 bp, respectively (Note that loci with trimmed alignments shorter than 250 bp were removed).

Thus, the core of the trimming is the evaluation criterion.

Sequences were edited manually and trimmed using Sequencher 5.0 following the criteria: (i) trimming no more than 25% of the sequence length until the first 25 nucleotides would contain less than 5 ambiguities, and (ii) trimming no more than 25% of the sequence length until the first 25 nucleotides would contain less than 5 nucleotides with confidences below 25.

First, read trimming using base quality criteria applied in our pipeline increased the length of analyzed sequence adjacent to PstI sites (in average 90 bp), thereby increasing the mapping accuracy in the highly duplicated genome and allowing us to perform SNP detection in larger genomic regions.