Evidence map›Paper›PMID 31024610›Full record

ArticleFrontiers in genetics2019

A Novel Approach to Clustering Genome Sequences Using Inter-nucleotide Covariance.

Rui Dong, Lily He, Rong Lucy He, Stephen S-T Yau

Abstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Unsupervised identification of significant lineages of SARS-CoV-2 through scalable machine learning methods.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Geometric construction of viral genome space and its applications.Computational and structural biotechnology journal · 2021
    Article
  14. Whole-GenomeGenes · 2020
    Article
  15. Circular Clustering With Polar Coordinate Reconstruction.IEEE/ACM transactions on computational biology and bioinformatics
    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

4 authors.

Rui DongDepartment of Mathematical Sciences, Tsinghua University, Beijing, China.
Lily HeDepartment of Mathematical Sciences, Tsinghua University, Beijing, China.
Rong Lucy HeDepartment of Biological Sciences, Chicago State University, Chicago, IL, United States.
Stephen S-T YauDepartment of Mathematical Sciences, Tsinghua University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classification of DNA sequences is an important issue in the bioinformatics study, yet most existing methods for phylogenetic analysis including Multiple Sequence Alignment (MSA) are time-consuming and computationally expensive. The alignment-free methods are popular nowadays, whereas the manual intervention in those methods usually decreases the accuracy. Also, the interactions among nucleotides are neglected in most methods. Here we propose a new Accumulated Natural Vector (ANV) method which represents each DNA sequence by a point in ℝ

Indexed as

accumulated natural vectoralignment-freegenomesinter-nucleotide covariancephylogenetic analysis

Identifiers

PMID31024610
PMCPMC6465635

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.