Evidence map›Paper›PMID 21918634›Full record

ArticleAdvances and applications in bioinformatics and chemistry : AABC2011

LifePrint: a novel k-tuple distance method for construction of phylogenetic trees.

Fabián Reyes-Prieto, Adda J García-Chéquer, Hueman Jaimes-Díaz, Janet Casique-Almazán, Juana M Espinosa-Lara, Rosaura Palma-Orozco, Alfonso Méndez-Tenorio, Rogelio Maldonado-Rodríguez, Kenneth L Beattie

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Article in Advances and applications in bioinformatics and chemistry : AABC, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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4 citing papers in PubMed.

  1. Whole Genome Sequence and Phylogenetic Analysis ShowFrontiers in cellular and infection microbiology · 2017
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5 · Who and what money

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9 authors.

Fabián Reyes-PrietoLaboratory of Biotechnology and Genomic Bioinformatics, Department of Biochemistry, National School of Biological Sciences, Mexico City, Mexico.
Adda J García-Chéquer
Hueman Jaimes-Díaz
Janet Casique-Almazán
Juana M Espinosa-Lara
Rosaura Palma-Orozco
Alfonso Méndez-Tenorio
Rogelio Maldonado-Rodríguez
Kenneth L Beattie

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHere we describe LifePrint, a sequence alignment-independent k-tuple distance method to estimate relatedness between complete genomes.

methodsWe designed a representative sample of all possible DNA tuples of length 9 (9-tuples). The final sample comprises 1878 tuples (called the LifePrint set of 9-tuples; LPS9) that are distinct from each other by at least two internal and noncontiguous nucleotide differences. For validation of our k-tuple distance method, we analyzed several real and simulated viroid genomes. Using different distance metrics, we scrutinized diverse viroid genomes to estimate the k-tuple distances between these genomic sequences. Then we used the estimated genomic k-tuple distances to construct phylogenetic trees using the neighbor-joining algorithm. A comparison of the accuracy of LPS9 and the previously reported 5-tuple method was made using symmetric differences between the trees estimated from each method and a simulated "true" phylogenetic tree.

resultsThe identified optimal search scheme for LPS9 allows only up to two nucleotide differences between each 9-tuple and the scrutinized genome. Similarity search results of simulated viroid genomes indicate that, in most cases, LPS9 is able to detect single-base substitutions between genomes efficiently. Analysis of simulated genomic variants with a high proportion of base substitutions indicates that LPS9 is able to discern relationships between genomic variants with up to 40% of nucleotide substitution.

conclusionOur LPS9 method generates more accurate phylogenetic reconstructions than the previously proposed 5-tuples strategy. LPS9-reconstructed trees show higher bootstrap proportion values than distance trees derived from the 5-tuple method.

Indexed as

phylogenysequence alignmentsimilarity searchtupleviroid

Identifiers

PMID21918634
PMCPMC3169951

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.