Evidence map›Paper›PMID 36120669›Full record

ArticleComputational intelligence and neuroscience2022

Lightweight Pattern Matching Method for DNA Sequencing in Internet of Medical Things.

J A M Rexie, Kumudha Raimond, Mythily Murugaaboopathy, D Brindha, Henock Mulugeta

Abstract read
In one paragraph

Article in Computational intelligence and neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

J A M RexieDepartment of Computer Science and Engineering, Karunya Institute of Technology and Sciences, Coimbatore, India.ORCID https://orcid.org/0000-0001-8785-2385
Kumudha RaimondDepartment of Computer Science and Engineering, Karunya Institute of Technology and Sciences, Coimbatore, India.
Mythily MurugaaboopathyDepartment of Computer Science and Engineering, Karunya Institute of Technology and Sciences, Coimbatore, India.
D BrindhaDepartment of Computer Science and Engineering, Karunya Institute of Technology and Sciences, Coimbatore, India.
Henock MulugetaComputer Engineering, Cybersecurity and AI School of Information Technology and Engineering (SiTE), Addis Ababa Institute of Technology, Addis Ababa, Ethiopia.ORCID https://orcid.org/0000-0002-0467-8121

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An area of medical science, that is, gaining prominence, is DNA sequencing. Genetic mutations responsible for the disease have been detected using DNA sequencing. The research is focusing on pattern identification methodologies for dealing with DNA-sequencing problems relating to various applications. A few examples of such problems are alignment and assembly of short reads from next generation sequencing (NGS), comparing DNA sequences, and determining the frequency of a pattern in a sequence. The approximate matching of DNA sequences is also well suited for many applications equivalent to the exact matching of the sequence since the DNA sequences are often subject to mutation. Consequently, recognizing pattern similarity becomes necessary. Furthermore, it can also be used in virtually every application that calls for pattern matching, for example, spell-checking, spam filtering, and search engines. According to the traditional approach, finding a similar pattern in the case where the sequence length is

Indexed as

AlgorithmsInternetDNASequence AlignmentSequence Analysis, DNADNA

Identifiers

PMID36120669
PMCPMC9477578

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.