Abstract
Nucleotide insertions and deletions (indels) are responsible for gaps in the sequence alignments. Indel is one of the major sources of evolutionary change at the molecular level. We have examined the patterns of insertions and deletions in the 19 mammalian genomes, and found that deletion events are more common than insertions in the mammalian genomes. Both the number of insertions and deletions decrease rapidly when the gap length increases and single nucleotide indel is the most frequent in all indel events. The frequencies of both insertions and deletions can be described well by power law.
Keywords: Insertion, deletion, gap, indel, mammalian genome
Current Genomics
Title: Patterns of Insertion and Deletion in Mammalian Genomes
Volume: 8 Issue: 6
Author(s): Shiheng Tao, Yanhui Fan, Wenjuan Wang, Guoji Ma, Lijing Liang and Qi Shi
Affiliation:
Keywords: Insertion, deletion, gap, indel, mammalian genome
Abstract: Nucleotide insertions and deletions (indels) are responsible for gaps in the sequence alignments. Indel is one of the major sources of evolutionary change at the molecular level. We have examined the patterns of insertions and deletions in the 19 mammalian genomes, and found that deletion events are more common than insertions in the mammalian genomes. Both the number of insertions and deletions decrease rapidly when the gap length increases and single nucleotide indel is the most frequent in all indel events. The frequencies of both insertions and deletions can be described well by power law.
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Cite this article as:
Tao Shiheng, Fan Yanhui, Wang Wenjuan, Ma Guoji, Liang Lijing and Shi Qi, Patterns of Insertion and Deletion in Mammalian Genomes, Current Genomics 2007; 8 (6) . https://dx.doi.org/10.2174/138920207783406479
DOI https://dx.doi.org/10.2174/138920207783406479 |
Print ISSN 1389-2029 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5488 |
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