Evidence map›Paper›PMID 28373895›Full record

ArticleAlgorithms for molecular biology : AMB2017

Aligning coding sequences with frameshift extension penalties.

Safa Jammali, Esaie Kuitche, Ayoub Rachati, François Bélanger, Michelle Scott, Aïda Ouangraoua

Open access · goldAbstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. From pairwise to multiple spliced alignment.Bioinformatics advances · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Safa JammaliDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC J1K2R1 Canada.ORCID 0000-0002-7709-1639
Esaie KuitcheDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC J1K2R1 Canada.
Ayoub RachatiDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC J1K2R1 Canada.
François BélangerDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC J1K2R1 Canada.
Michelle ScottDépartement de biochimie, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, QC J1E4K8 Canada.
Aïda OuangraouaDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC J1K2R1 Canada.
Université de Sherbrooke · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFrameshift translation is an important phenomenon that contributes to the appearance of novel coding DNA sequences (CDS) and functions in gene evolution, by allowing alternative amino acid translations of gene coding regions. Frameshift translations can be identified by aligning two CDS, from a same gene or from homologous genes, while accounting for their codon structure. Two main classes of algorithms have been proposed to solve the problem of aligning CDS, either by amino acid sequence alignment back-translation, or by simultaneously accounting for the nucleotide and amino acid levels. The former does not allow to account for frameshift translations and up to now, the latter exclusively accounts for frameshift translation initiation, not considering the length of the translation disruption caused by a frameshift.

resultsWe introduce a new scoring scheme with an algorithm for the pairwise alignment of CDS accounting for frameshift translation initiation and length, while simultaneously considering nucleotide and amino acid sequences. The main specificity of the scoring scheme is the introduction of a penalty cost accounting for frameshift extension length to compute an adequate similarity score for a CDS alignment. The second specificity of the model is that the search space of the problem solved is the set of all feasible alignments between two CDS. Previous approaches have considered restricted search space or additional constraints on the decomposition of an alignment into length-3 sub-alignments. The algorithm described in this paper has the same asymptotic time complexity as the classical Needleman-Wunsch algorithm.

conclusionsWe compare the method to other CDS alignment methods based on an application to the comparison of pairs of CDS from homologous

Indexed as

Coding DNA sequences pairwise alignmentDynamic programmingFrameshifts

Identifiers

PMID28373895
PMCPMC5374649
OpenAlexW2544103171

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.