Evidence map›Paper›PMID 21123221›Full record

ArticleBioinformatics (Oxford, England)2011

maxAlike: maximum likelihood-based sequence reconstruction with application to improved primer design for unknown sequences.

Peter Menzel, Peter F Stadler, Jan Gorodkin

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Article in Bioinformatics (Oxford, England), 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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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Evolution and Phylogeny of MicroRNAs - Protocols, Pitfalls, and Problems.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  2. phoD Alkaline Phosphatase Gene Diversity in Soil.Applied and environmental microbiology · 2015
    Article
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5 · Who and what money

Authors and funding

3 authors.

Peter MenzelCenter for non-coding RNA in Technology and Health, IBHV, University of Copenhagen, Grønnegårdsvej 3, DK-1870 Frederiksberg, Denmark.
Peter F Stadler
Jan Gorodkin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationThe task of reconstructing a genomic sequence from a particular species is gaining more and more importance in the light of the rapid development of high-throughput sequencing technologies and their limitations. Applications include not only compensation for missing data in unsequenced genomic regions and the design of oligonucleotide primers for target genes in species with lacking sequence information but also the preparation of customized queries for homology searches.

resultsWe introduce the maxAlike algorithm, which reconstructs a genomic sequence for a specific taxon based on sequence homologs in other species. The input is a multiple sequence alignment and a phylogenetic tree that also contains the target species. For this target species, the algorithm computes nucleotide probabilities at each sequence position. Consensus sequences are then reconstructed based on a certain confidence level. For 37 out of 44 target species in a test dataset, we obtain a significant increase of the reconstruction accuracy compared to both the consensus sequence from the alignment and the sequence of the nearest phylogenetic neighbor. When considering only nucleotides above a confidence limit, maxAlike is significantly better (up to 10%) in all 44 species. The improved sequence reconstruction also leads to an increase of the quality of PCR primer design for yet unsequenced genes: the differences between the expected T(m) and real T(m) of the primer-template duplex can be reduced by ~26% compared with other reconstruction approaches. We also show that the prediction accuracy is robust to common distortions of the input trees. The prediction accuracy drops by only 1% on average across all species for 77% of trees derived from random genomic loci in a test dataset. AVAILABILITY: maxAlike is available for download and web server at: http://rth.dk/resources/maxAlike.

Indexed as

AlgorithmsAnimalsDNA PrimersHumansImage Processing, Computer-AssistedPolymerase Chain ReactionSequence Analysis, DNASequence HomologySoftwareDNA Primers

Identifiers

PMID21123221
PMCPMC3031029

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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.