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MicroRNA categorization using sequence motifs and k-mers.

Identifieur interne : 000C24 ( PubMed/Checkpoint ); précédent : 000C23; suivant : 000C25

MicroRNA categorization using sequence motifs and k-mers.

Auteurs : Malik Yousef [Israël] ; Waleed Khalifa [Israël] ; Lhan Erkin Acar [Turquie] ; Jens Allmer [Turquie]

Source :

RBID : pubmed:28292266

Descripteurs français

English descriptors

Abstract

Post-transcriptional gene dysregulation can be a hallmark of diseases like cancer and microRNAs (miRNAs) play a key role in the modulation of translation efficiency. Known pre-miRNAs are listed in miRBase, and they have been discovered in a variety of organisms ranging from viruses and microbes to eukaryotic organisms. The computational detection of pre-miRNAs is of great interest, and such approaches usually employ machine learning to discriminate between miRNAs and other sequences. Many features have been proposed describing pre-miRNAs, and we have previously introduced the use of sequence motifs and k-mers as useful ones. There have been reports of xeno-miRNAs detected via next generation sequencing. However, they may be contaminations and to aid that important decision-making process, we aimed to establish a means to differentiate pre-miRNAs from different species.

DOI: 10.1186/s12859-017-1584-1
PubMed: 28292266


Affiliations:


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pubmed:28292266

Le document en format XML

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<div type="abstract" xml:lang="en">Post-transcriptional gene dysregulation can be a hallmark of diseases like cancer and microRNAs (miRNAs) play a key role in the modulation of translation efficiency. Known pre-miRNAs are listed in miRBase, and they have been discovered in a variety of organisms ranging from viruses and microbes to eukaryotic organisms. The computational detection of pre-miRNAs is of great interest, and such approaches usually employ machine learning to discriminate between miRNAs and other sequences. Many features have been proposed describing pre-miRNAs, and we have previously introduced the use of sequence motifs and k-mers as useful ones. There have been reports of xeno-miRNAs detected via next generation sequencing. However, they may be contaminations and to aid that important decision-making process, we aimed to establish a means to differentiate pre-miRNAs from different species.</div>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Post-transcriptional gene dysregulation can be a hallmark of diseases like cancer and microRNAs (miRNAs) play a key role in the modulation of translation efficiency. Known pre-miRNAs are listed in miRBase, and they have been discovered in a variety of organisms ranging from viruses and microbes to eukaryotic organisms. The computational detection of pre-miRNAs is of great interest, and such approaches usually employ machine learning to discriminate between miRNAs and other sequences. Many features have been proposed describing pre-miRNAs, and we have previously introduced the use of sequence motifs and k-mers as useful ones. There have been reports of xeno-miRNAs detected via next generation sequencing. However, they may be contaminations and to aid that important decision-making process, we aimed to establish a means to differentiate pre-miRNAs from different species.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">To achieve distinction into species, we used one species' pre-miRNAs as the positive and another species' pre-miRNAs as the negative training and test data for the establishment of machine learned models based on sequence motifs and k-mers as features. This approach resulted in higher accuracy values between distantly related species while species with closer relation produced lower accuracy values.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">We were able to differentiate among species with increasing success when the evolutionary distance increases. This conclusion is supported by previous reports of fast evolutionary changes in miRNAs since even in relatively closely related species a fairly good discrimination was possible.</AbstractText>
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<name sortKey="Yousef, Malik" sort="Yousef, Malik" uniqKey="Yousef M" first="Malik" last="Yousef">Malik Yousef</name>
</noRegion>
<name sortKey="Khalifa, Waleed" sort="Khalifa, Waleed" uniqKey="Khalifa W" first="Waleed" last="Khalifa">Waleed Khalifa</name>
</country>
<country name="Turquie">
<noRegion>
<name sortKey="Acar, Lhan Erkin" sort="Acar, Lhan Erkin" uniqKey="Acar " first=" Lhan Erkin" last="Acar"> Lhan Erkin Acar</name>
</noRegion>
<name sortKey="Allmer, Jens" sort="Allmer, Jens" uniqKey="Allmer J" first="Jens" last="Allmer">Jens Allmer</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000C24 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 000C24 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    MersV1
   |flux=    PubMed
   |étape=   Checkpoint
   |type=    RBID
   |clé=     pubmed:28292266
   |texte=   MicroRNA categorization using sequence motifs and k-mers.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i   -Sk "pubmed:28292266" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a MersV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021