Evidence map›Paper›PMID 34132752›Full record

ArticleBioinformatics (Oxford, England)2021

SANS serif: alignment-free, whole-genome-based phylogenetic reconstruction.

Andreas Rempel, Roland Wittler

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

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

19 citing papers in PubMed.

  1. Genomic characterization ofMicrobiology (Reading, England) · 2026
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  11. Methods for Pangenomic Core Detection.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. Article
  13. Article
  14. phyBWT2: phylogeny reconstruction via eBWT positional clustering.Algorithms for molecular biology : AMB · 2023
    Article
  15. Article
  16. The Genome of the Soybean Gall Midge (bioRxiv : the preprint server for biology · 2023
    Article
  17. Article
  18. Article
  19. 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

2 authors.

Andreas RempelGenome Informatics, Faculty of Technology and Center for Biotechnology, Bielefeld University, 33615 Bielefeld, Germany.ORCID 0000-0003-0609-5621
Roland WittlerGenome Informatics, Faculty of Technology and Center for Biotechnology, Bielefeld University, 33615 Bielefeld, Germany.ORCID 0000-0002-2249-9880

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summarySANS serif is a novel software for alignment-free, whole-genome-based phylogeny estimation that follows a pangenomic approach to efficiently calculate a set of splits in a phylogenetic tree or network. AVAILABILITY AND IMPLEMENTATION: Implemented in C++ and supported on Linux, MacOS and Windows. The source code is freely available for download at https://gitlab.ub.uni-bielefeld.de/gi/sans. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

GenomeSoftwarePhylogeny

Identifiers

PMID34132752
PMCPMC8665756

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.