Evidence map›Paper›PMID 23335788›Full record

ArticleNucleic acids research2013

Co-phylog: an assembly-free phylogenomic approach for closely related organisms.

Huiguang Yi, Li Jin

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed.

  1. Article
  2. Article
  3. Sequence similarity estimation by random subsequence sketching.bioRxiv : the preprint server for biology · 2025
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  4. Review
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  6. Article
  7. A k-mer-Based Estimator of the Substitution Rate Between Repetitive Sequences.Algorithms in bioinformatics : ... International Workshop, WABI ..., proceedings. WABI (Workshop) · 2025
    Article
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. How to optimally sample a sequence for rapid analysis.Bioinformatics (Oxford, England) · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Space-efficient representation of genomic k-mer count tables.Algorithms for molecular biology : AMB · 2022
    Article
  20. In-depth investigation of the point mutation pattern of HIV-1.Frontiers in cellular and infection microbiology · 2022
    Article

5 more citing papers are in PubMed but not listed here.

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.

Huiguang YiState Key Laboratory of Genetic Engineering and Ministry of Education Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai 200433, China. yhg926@gmail.com
Li Jin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the advent of high-throughput sequencing technologies, the rapid generation and accumulation of large amounts of sequencing data pose an insurmountable demand for efficient algorithms for constructing whole-genome phylogenies. The existing phylogenomic methods all use assembled sequences, which are often not available owing to the difficulty of assembling short-reads; this obstructs phylogenetic investigations on species without a reference genome. In this report, we present co-phylog, an assembly-free phylogenomic approach that creates a 'micro-alignment' at each 'object' in the sequence using the 'context' of the object and calculates pairwise distances before reconstructing the phylogenetic tree based on those distances. We explored the parameters' usages and the optimal working range of co-phylog, assessed co-phylog using the simulated next-generation sequencing (NGS) data and the real NGS raw data. We also compared co-phylog method with traditional alignment and alignment-free methods and illustrated the advantages and limitations of co-phylog method. In conclusion, we demonstrated that co-phylog is efficient algorithm and that it delivers high resolution and accurate phylogenies using whole-genome unassembled sequencing data, especially in the case of closely related organisms, thereby significantly alleviating the computational burden in the genomic era.

Indexed as

AlgorithmsPhylogenyComputer SimulationEnterobacteriaceaeEscherichiaGammaproteobacteriaGenome, BacterialGenomicsHigh-Throughput Nucleotide SequencingSequence AlignmentShigellaSoftware

Identifiers

PMID23335788
PMCPMC3627563

What OpenQuestion holds

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Registered trials

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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.