2013
DOI: 10.1093/bib/bbt052
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Alignment-free genetic sequence comparisons: a review of recent approaches by word analysis

Abstract: Modern sequencing and genome assembly technologies have provided a wealth of data, which will soon require an analysis by comparison for discovery. Sequence alignment, a fundamental task in bioinformatics research, may be used but with some caveats. Seminal techniques and methods from dynamic programming are proving ineffective for this work owing to their inherent computational expense when processing large amounts of sequence data. These methods are prone to giving misleading information because of genetic r… Show more

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Cited by 118 publications
(84 citation statements)
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“…Other software, such as Andi, computes rapid local alignments between each genome and defines the distance based on mismatches within each alignment (184). Haubold (185), as well as Bonham-Carter et al (186), has written excellent reviews of alignment-free methods that can be referred to for additional details.…”
Section: Phylogenetics To Phylogenomicsmentioning
confidence: 99%
“…Other software, such as Andi, computes rapid local alignments between each genome and defines the distance based on mismatches within each alignment (184). Haubold (185), as well as Bonham-Carter et al (186), has written excellent reviews of alignment-free methods that can be referred to for additional details.…”
Section: Phylogenetics To Phylogenomicsmentioning
confidence: 99%
“…Furthermore, frequency analysis is especially well suited for comparing large data sets and discovery, as it embraces convenient techniques of network analysis to ascertain natural patterns [26,27]. Here, we discuss the collection of frequency information, which is later used to build networks to discover PTM and RS biases.…”
Section: Computing Frequenciesmentioning
confidence: 99%
“…Eisen (1998), Yi et al (2007), and Hatfull et al (2010) clustered genomes by various types of statistical information from DNA microarray data. Bonham-Carter et al (2014) summarized 14 alignment-free genetic sequence comparison methods. However, all these methods only utilize features from short string and probability information, without any features from the transformed space, such as frequency domain.…”
Section: Related Workmentioning
confidence: 99%