Evidence map›Paper›PMID 39281454›Full record

ArticleHeliyon2024

DNA N-gram analysis framework (DNAnamer): A generalized N-gram frequency analysis framework for the supervised classification of DNA sequences.

John S Malamon

Abstract read
In one paragraph

Article in Heliyon, 2024. 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

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

2 citing papers in PubMed.

  1. Article
  2. Review
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

1 author.

John S MalamonUniversity of Colorado Anschutz Medical Campus, Department of Surgery, Division of Transplant Surgery, 1635 Aurora Court, Aurora, CO, 80045, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 1948, Claude Shannon published a mathematical system describing the probabilistic relationships between the letters of a natural language and their subsequent order or syntax structure. By counting unique, reoccurring sequences of letters called N-grams, this language model was used to generate recognizable English sentences from N-gram frequency probability tables. More recently, N-gram analysis methodologies have been successfully applied to address many complex problems in a variety of domains, from language processing to genomics. One such example is the common use of N-gram frequency patterns and supervised classification models to determine authorship and plagiarism. In this paradigm, DNA is a language model where nucleotides are analogous to the letters of a word and nucleotide N-grams are analogous to the words of a sentence. Because DNA contains highly conserved and identifiable nucleotide sequence frequency patterns, this approach can be applied to a variety of classification and data reduction problems, such as identifying species based on unknown DNA segments. Other useful applications of this methodology include the identification of functional gene elements, microorganisms, sequence contamination, and sequencing artifacts. To this end, I present DNAnamer, a generalized and extensible methodological framework and analysis toolkit for the supervised classification of DNA sequences based on their N-gram frequency patterns.

Identifiers

PMID39281454
PMCPMC11399624

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.