Sequence alignment

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Sequence Alignment

Sequence alignment is a method used in bioinformatics to arrange the sequences of DNA, RNA, or protein to identify regions of similarity. These similarities may be a result of functional, structural, or evolutionary relationships between the sequences.

Pronunciation

  • Sequence: /ˈsiːkwəns/
  • Alignment: /əˈlʌɪnmənt/

Etymology

The term "sequence alignment" is derived from the English words "sequence" and "alignment". "Sequence" comes from the Latin word "sequentia", meaning "a following", and "alignment" comes from the French word "aligner", meaning "to line up".

Related Terms

Description

In bioinformatics, sequence alignment is a way of arranging the sequences of DNA, RNA, or protein to identify regions of similarity that may be a consequence of functional, structural, or evolutionary relationships among the sequences. Aligned sequences of nucleotide or amino acid residues are typically represented as rows within a matrix. Gaps are inserted between the sequences to optimize the alignment and to introduce gaps in the sequences.

Sequence alignment can be used to assess similarity, to infer phylogenetic relationships, to find conserved sequences and to predict the function and structure of unknown sequences. There are two main types of sequence alignment: pairwise sequence alignment and multiple sequence alignment.

Methods

There are various methods used to perform sequence alignment. The choice of the method depends on the number of sequences to be aligned, the assumed evolutionary distance between them and the purpose of the alignment. The most common methods are:

Applications

Sequence alignment is used in various fields of biology. It is fundamental to the annotation of genome sequencing projects, it is used in comparative genomics, and it is central to the field of phylogenetics.

External links

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