在我们的软件中，当计算多重比对中每个残基位置的信息量时，空位被考虑。

In our software gaps are accounted for when calculating the information content present at each residue position in a multiple alignment.

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高效的RNA序列操作(例如多重比对)需要被RNA结构折叠的规则限制。

Efficient RNA sequence manipulations (such as multiple alignments) need to be constrained by rules of RNA structure folding.

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