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This manual describes all parameters, input and output data supported by this Dialign online service. The variation and count of parameters, the parameter range and input/ output types can differ from the standalone used program.

AA alignment

DNA alignment

RNA alignment

In-/Output values

INPUT :: aa_sequences

A set of amino acid sequences to be aligned.

INPUT :: dna_sequences

Deoxyribonucleic acid sequences to be aligned.

INPUT :: rna_sequences

Ribonucleic acid sequences to be aligned.

OUTPUT :: AA alignment

Multiples Amino Acid Alignment.

OUTPUT :: DNA alignment

Multiples deoxyribonucleic acid alignment.

OUTPUT :: RNA alignment

Multiples ribonucleic acid alignment.

Parameter

Name Description
threshold

As described in our papers, DIALIGN constructs alignments from gapfree pairs of segments of the sequences. Such segment pairs are referred to as diagonals.

Every possible diagonal is given a so-called weight reflecting the degree of similarity among the two segments involved. The overall score of an alignment ist then defined as the sum of weights of the diagonals it consists of and the program tries to find an alignment with maximum score -- in other words: the program tries to find a consistent collection of diagonals with maximum sum of weights. This novel scoring scheme for alignments is the basic difference between DIALIGN and other global or local alignment methods. Note that DIALIGN does not employ any kind of gap penalty.

It is possible to use a threshold T for the quality of the diagonals. In this case, diagonals are considered only if their weights exceed this threshold, and regions of lower similarity are ignored.

In the first version of the program (DIALIGN 1), this threshold was in many situations absolutely necessary to obtain meaningful alignments. By contrast, DIALIGN 2 should produce reasonable alignments without a threshold, i.e. with T = 0. This is the most important difference between DIALIGN 2 and the first version of the program.

Nevertheless, it is still possible to use a threshold T, so it is up to the user to experience with this option.

nucleic acid sequence handling If (possibly) coding nucleic acid sequences are to be aligned, DIALIGN optionally translates the compared `nucleic acid segments' to `peptide segments' according to the genetic code -- without (necessarily) presupposing any of the three possible reading frames, so all three of them get checked for significant similarity. In this case, the similarity among segments will be assessed on the `peptide level' rather than on the `nucleic acid level'. We strongly recommend this option if nucleic acid sequences are expected to contain protein coding regions, as it will significantly increase the sensitivity of the alignment procedure in such cases.