Evidence map›Paper›PMID 34447886›Full record

ArticleMitochondrial DNA. Part B, Resources2021

Aln2tbl: building a mitochondrial features table from a assembly alignment in fasta format.

Joan Pons, Juan José Ensenyat, Pere Bover, Miquel Serra, Francesco Nardi

Abstract read
In one paragraph

Article in Mitochondrial DNA. Part B, Resources, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. Article
  2. The complete mitochondrial genome of the shining leaf chaferMitochondrial DNA. Part B, Resources · 2024
    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

5 authors.

Joan PonsDepartament de Biodiversitat Animal i Microbiana, Institut Mediterrani d'Estudis Avançats (IMEDEA, CSIC-UIB), Esporles, Spain.ORCID https://orcid.org/0000-0002-4683-8840
Juan José EnsenyatTecnologies de la informació i la comunicació, Institut Mediterrani d'Estudis Avançats (IMEDEA, CSIC-UIB), Esporles, Spain.ORCID https://orcid.org/0000-0003-4970-0668
Pere BoverInstituto Universitario de Investigación en Ciencias Ambientales (IUCA), Grupo Aragosaurus - Departamento de Ciencias de la Tierra, Facultad de Ciencias, Universidad de Zaragoza, Zaragoza, Spain.ORCID https://orcid.org/0000-0003-2942-2840
Miquel SerraTecnologies de la informació i la comunicació, Institut Mediterrani d'Estudis Avançats (IMEDEA, CSIC-UIB), Esporles, Spain.ORCID https://orcid.org/0000-0002-1889-6373
Francesco NardiDepartment of Life Sciences, University of Siena, Siena, Italy.ORCID https://orcid.org/0000-0003-0271-9855

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sequencing, annotation and analysis of complete mitochondrial genomes is an important research tool in phylogeny and evolution. Starting with the primary sequence, genes/features are generally annotated automatically to obtain preliminary annotations in the form of a feature table. Further manual curation in a graphic alignment editor is nevertheless necessary to revise annotations. As such, the automatically generated feature table is invalidated and has to be modified manually before submission to data banks. We developed aln2tbl.py, a python script that recreates a feature table from a manually refined alignment of genes mapped on the mitochondrial genome in fasta format. The feature table is populated with notes and annotations specific to mitochondrial genomes. The table can be used to create a sqn file to be submitted directly to data banks. In summary, our scripts fills one gap in the available toolbox and, combined with other software, allows the automation of the entire process, from primary sequence to annotated genome submission, even if a manual curation step is conducted in a visual sequence editor.

Indexed as

feature tableGenBank submissiongene annotationMitochondrial genomePython

Identifiers

PMID34447886
PMCPMC8386716

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.