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The evaluation of the sequences' motion intensity is shown in Table 3.

This was the case during our visual evaluation of the sequences.

Authors' visual evaluation of the sequences played back at frame rates of 15 fps and 30 fps revealed highest flicker in the sequences generated using Floyd and Steinberg [14] error diffusion.

Evaluation of the sequence patterns and data entry were independently performed by two observers.

The results of the quality evaluation of the sequencing data were excellent, with bases being distributed evenly; thus, we continued our analyses.

Evaluation of the sequence alignment led to the finding that 89 out of 94 RNA11 sequences can form a short helix with at least three base pairs (Fig.  1).

For a comprehensive evaluation of the sequence data, we expanded our data set with orthologous sequences, already deposited at GenBank, from two L. ruficaudatus and one L. dorsalis.

Our careful re-evaluation of the sequence data confirmed that there are indeed 59 polymorphic sites, out of which 43 are replacements and 16 are synonymous.

Evaluation of the sequence logos dismisses Ty1/Copia and Bel/Pao LTRCAPs from this relationship because these 2 families exhibit phenotypic features distinguishing them from other CAPs.

The following procedures were performed with Solexa to summarize the data: evaluation of the sequencing quality, calculation of the length distribution of small RNA reads, and filtration of the reads contaminated by rRNA, tRNA, mRNA, snRNA, and snoRNA.

Figure 2 shows the final multiple sequence alignment (MSA) of the HEN1 family, which was refined based on the results of structure prediction and evaluation of the sequence-structure fit on the three-dimensional level (see below).

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