Evidence map›Paper›PMID 25510498›Full record

ArticleNucleic acids research2015

T-lex2: genotyping, frequency estimation and re-annotation of transposable elements using single or pooled next-generation sequencing data.

Anna-Sophie Fiston-Lavier, Maite G Barrón, Dmitri A Petrov, Josefa González

Abstract readValidation Study
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

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  8. Finding and Characterizing Repeats in Plant Genomes.Methods in molecular biology (Clifton, N.J.) · 2022
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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

4 authors.

Anna-Sophie Fiston-LavierDepartment of Biology, Stanford University, Stanford, CA 94305-5020, USA Institut des Sciences de l'Evolution de Montpellier (ISEM), UMR5554 CNRS-Université Montpellier 2, France asfiston@univ-montp2.fr.
Maite G BarrónGenomics, Bioinformatics and Evolution Group, Institut de Biotecnologia i de Biomedicina - IBB/Department of Genetics and Microbiology, Campus Universitat Autònoma de Barcelona, Bellaterra 08193, Spain Institute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Barcelona 08003, Spain.
Dmitri A PetrovDepartment of Biology, Stanford University, Stanford, CA 94305-5020, USA.
Josefa GonzálezInstitute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Barcelona 08003, Spain.

Funding

Population Genomics of Adaptive Transposition in DrosophilaR01GM089926 · NIGMS · STANFORD UNIVERSITY · PI PETROV, DMITRI · 2010 to 2013
$969k
NIGMS NIH HHS R01GM089926
6 · The paper itself

Abstract

Transposable elements (TEs) constitute the most active, diverse and ancient component in a broad range of genomes. Complete understanding of genome function and evolution cannot be achieved without a thorough understanding of TE impact and biology. However, in-depth analysis of TEs still represents a challenge due to the repetitive nature of these genomic entities. In this work, we present a broadly applicable and flexible tool: T-lex2. T-lex2 is the only available software that allows routine, automatic and accurate genotyping of individual TE insertions and estimation of their population frequencies both using individual strain and pooled next-generation sequencing data. Furthermore, T-lex2 also assesses the quality of the calls allowing the identification of miss-annotated TEs and providing the necessary information to re-annotate them. The flexible and customizable design of T-lex2 allows running it in any genome and for any type of TE insertion. Here, we tested the fidelity of T-lex2 using the fly and human genomes. Overall, T-lex2 represents a significant improvement in our ability to analyze the contribution of TEs to genome function and evolution as well as learning about the biology of TEs. T-lex2 is freely available online at http://sourceforge.net/projects/tlex.

Indexed as

High-Throughput Nucleotide SequencingInterspersed Repetitive SequencesSequence Analysis, DNASoftwareAnimalsDrosophila melanogasterGenome, HumanGenome, InsectGenotyping TechniquesHumansMolecular Sequence Annotation

Identifiers

PMID25510498
PMCPMC4344482

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.