Evidence map›Paper›PMID 39441245›Full record

ArticleBriefings in bioinformatics2024

Advancing microbial diagnostics: a universal phylogeny guided computational algorithm to find unique sequences for precise microorganism detection.

Gulshan Kumar Sharma, Rakesh Sharma, Kavita Joshi, Sameer Qureshi, Shubhita Mathur, Sharad Sinha, Samit Chatterjee, Vandana Nunia

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Fast detection of unique genomic regions.Computational and structural biotechnology journal · 2025
    Review
  5. 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

8 authors.

Gulshan Kumar SharmaMalaviya National Institute of Technology, Jawahar Lal Nehru Marg, Jhalana Gram, Malviya Nagar, Jaipur, Rajasthan 302017, India.
Rakesh SharmaCentre for Converging Technologies, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Kavita JoshiDepartment of Zoology, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Sameer QureshiDepartment of Zoology, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Shubhita MathurDepartment of Zoology, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Sharad SinhaDepartment of Mathematics, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Samit ChatterjeeDepartment of Zoology, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.
Vandana NuniaDepartment of Zoology, University of Rajasthan, Jawahar Lal Nehru Marg, Talvandi, Jaipur, Rajasthan 302004, India.ORCID 0000-0003-0988-3359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequences derived from organisms sharing common evolutionary origins exhibit similarity, while unique sequences, absent in related organisms, act as good diagnostic marker candidates. However, the approach focused on identifying dissimilar regions among closely-related organisms poses challenges as it requires complex multiple sequence alignments, making computation and parsing difficult. To address this, we have developed a biologically inspired universal NAUniSeq algorithm to find the unique sequences for microorganism diagnosis by traveling through the phylogeny of life. Mapping through a phylogenetic tree ensures a low number of cross-contamination and false positives. We have downloaded complete taxonomy data from Taxadb database and sequence data from National Center for Biotechnology Information Reference Sequence Database (NCBI-Refseq) and, with the help of NetworkX, created a phylogenetic tree. Sequences were assigned over the graph nodes, k-mers were created for target and non-target nodes and search was performed over the graph using the depth first search algorithm. In a memory efficient alternative NoSQL approach, we created a collection of Refseq sequences in MongoDB database using tax-id and path of FASTA files. We queried the MongoDB collection for the target and non-target sequences. In both the approaches, we used an alignment free sliding window k-mer-based procedure that quickly compares k-mers of target and non-target sequences and returns unique sequences that are not present in the non-target. We have validated our algorithm with target nodes Mycobacterium tuberculosis, Neisseria gonorrhoeae, and Monkeypox and generated unique sequences. This universal algorithm is a powerful tool for generating diagnostic sequences, enabling the accurate identification of microbial strains with high phylogenetic precision.

Indexed as

AlgorithmsBacteriaPhylogenyComputational BiologyHumansMonkeypox virusMycobacterium tuberculosisNeisseria gonorrhoeaeSequence AlignmentSequence Analysis, DNASoftwaredepth first searchhash mapk-merphylogenetic treetaxonomyunique sequences

Identifiers

PMID39441245
PMCPMC11497845

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LicenceCC BY-NC
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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.