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Nineteen sequences were chosen for preliminary assessment on a panel of 15 animals.

shRNAs were designed to target the first and/or the longest ENSEMBL transcript of each hEIR gene and 1 3 shRNA target sequences were chosen per transcript.

The adjacent β strands of the found sequences were chosen as the peptide inhibitors of α-synuclein aggregation.

The regions belonging to the idiotypic VH and VL CDR3 sequences were chosen for the design of two synthetic mini-genes and arranged in high-level expression plasmids.

The pulse timing sequences were chosen to optimize detection of fission neutrons produced by thermal-neutron-induced fission in the SNM.

Sequences were chosen with identities under 40%%.

The sequences were chosen so as to comprise both clutter- and noise-dominated scenes.

Among the isolates, 66 of the sequences were chosen for mutational analysis.

Four sequences of five different RRs were randomly tested, and these sequences were chosen to alternate higher and lower respiratory frequencies (Figure 1).

A ten-fold dilution series of plasmids containing target DNA sequences were chosen as a calibration standard for establishing the standard curve.

One representative OTU (OTU05) of bacterial amoA genes was selected (Additional file 1: Table S4) and 23 AOB representative sequences were chosen and classified into five different clusters.

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