Evidence map›Paper›PMID 38444086›Full record

ArticleBioinformatics (Oxford, England)2024

KaMRaT: a C++ toolkit for k-mer count matrix dimension reduction.

Haoliang Xue, Mélina Gallopin, Camille Marchet, Ha N Nguyen, Yunfeng Wang, Antoine Lainé, Chloé Bessiere, Daniel Gautheret

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Haoliang XueI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.ORCID 0000-0002-1264-5303
Mélina GallopinI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.ORCID 0000-0002-2431-7825
Camille MarchetUniv. Lille, CNRS, Centrale Lille, UMR 9189 CRIStAL, F-59000 Lille, France.
Ha N NguyenI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.
Yunfeng WangI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.
Antoine LainéI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.
Chloé BessiereIRMB, University of Montpellier, 34295 Montpellier, France.
Daniel GautheretI2BC, Université Paris-Saclay, CNRS, CEA, 91190 Gif-sur-Yvette, France.ORCID 0000-0002-1508-8469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationKaMRaT is designed for processing large k-mer count tables derived from multi-sample, RNA-seq data. Its primary objective is to identify condition-specific or differentially expressed sequences, regardless of gene or transcript annotation.

resultsKaMRaT is implemented in C++. Major functions include scoring k-mers based on count statistics, merging overlapping k-mers into contigs and selecting k-mers based on their occurrence across specific samples. AVAILABILITY AND IMPLEMENTATION: Source code and documentation are available via https://github.com/Transipedia/KaMRaT.

Indexed as

AlgorithmsSoftwareDocumentationRNA-SeqSequence Analysis, DNA

Identifiers

PMID38444086
PMCPMC10942800

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.