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MarkerMiner 1.0: A new application for phylogenetic marker development using angiosperm transcriptomes.

Identifieur interne : 000029 ( PubMed/Checkpoint ); précédent : 000028; suivant : 000030

MarkerMiner 1.0: A new application for phylogenetic marker development using angiosperm transcriptomes.

Auteurs : Srikar Chamala [États-Unis] ; Nicolás García [Chili] ; Grant T. Godden [États-Unis] ; Vivek Krishnakumar [États-Unis] ; Ingrid E. Jordon-Thaden [États-Unis] ; Riet De Smet [Belgique] ; W Brad Barbazuk [États-Unis] ; Douglas E. Soltis [États-Unis] ; Pamela S. Soltis [États-Unis]

Source :

RBID : pubmed:25909041

Abstract

Targeted sequencing using next-generation sequencing (NGS) platforms offers enormous potential for plant systematics by enabling economical acquisition of multilocus data sets that can resolve difficult phylogenetic problems. However, because discovery of single-copy nuclear (SCN) loci from NGS data requires both bioinformatics skills and access to high-performance computing resources, the application of NGS data has been limited.

DOI: 10.3732/apps.1400115
PubMed: 25909041


Affiliations:


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pubmed:25909041

Le document en format XML

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<div type="abstract" xml:lang="en">Targeted sequencing using next-generation sequencing (NGS) platforms offers enormous potential for plant systematics by enabling economical acquisition of multilocus data sets that can resolve difficult phylogenetic problems. However, because discovery of single-copy nuclear (SCN) loci from NGS data requires both bioinformatics skills and access to high-performance computing resources, the application of NGS data has been limited.</div>
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<AbstractText Label="PREMISE OF THE STUDY" NlmCategory="OBJECTIVE">Targeted sequencing using next-generation sequencing (NGS) platforms offers enormous potential for plant systematics by enabling economical acquisition of multilocus data sets that can resolve difficult phylogenetic problems. However, because discovery of single-copy nuclear (SCN) loci from NGS data requires both bioinformatics skills and access to high-performance computing resources, the application of NGS data has been limited.</AbstractText>
<AbstractText Label="METHODS AND RESULTS" NlmCategory="RESULTS">We developed MarkerMiner 1.0, a fully automated, open-access bioinformatic workflow and application for discovery of SCN loci in angiosperms. Our new tool identified as many as 1993 SCN loci from transcriptomic data sampled as part of four independent test cases representing marker development projects at different phylogenetic scales.</AbstractText>
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<country name="Belgique">
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<name sortKey="De Smet, Riet" sort="De Smet, Riet" uniqKey="De Smet R" first="Riet" last="De Smet">Riet De Smet</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Belgique/explor/OpenAccessBelV2/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000029 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 000029 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Belgique
   |area=    OpenAccessBelV2
   |flux=    PubMed
   |étape=   Checkpoint
   |type=    RBID
   |clé=     pubmed:25909041
   |texte=   MarkerMiner 1.0: A new application for phylogenetic marker development using angiosperm transcriptomes.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i   -Sk "pubmed:25909041" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a OpenAccessBelV2 

Wicri

This area was generated with Dilib version V0.6.25.
Data generation: Thu Dec 1 00:43:49 2016. Site generation: Wed Mar 6 14:51:30 2024