Evidence map›Paper›PMID 25465054›Full record

ArticleBMC bioinformatics2014

VTBuilder: a tool for the assembly of multi isoform transcriptomes.

John Archer, Gareth Whiteley, Nicholas R Casewell, Robert A Harrison, Simon C Wagstaff

Abstract read
In one paragraph

Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  4. Toxins · 2021
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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

5 authors.

John ArcherDepartment of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA2, UK. john.archer.jpa@gmail.com.
Gareth WhiteleyDepartment of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA2, UK. gareth.whiteley@lstmed.ac.uk.
Nicholas R CasewellDepartment of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA2, UK. nicholas.casewell@lstmed.ac.uk.
Robert A HarrisonDepartment of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA2, UK. robert.harrison@lstmed.ac.uk.
Simon C WagstaffDepartment of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA2, UK. simon.wagstaff@lstmed.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/F012675/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/K500288/1
6 · The paper itself

Abstract

backgroundWithin many research areas, such as transcriptomics, the millions of short DNA fragments (reads) produced by current sequencing platforms need to be assembled into transcript sequences before they can be utilized. Despite recent advances in assembly software, creating such transcripts from read data harboring isoform variation remains challenging. This is because current approaches fail to identify all variants present or they create chimeric transcripts within which relationships between co-evolving sites and other evolutionary factors are disrupted. We present VTBuilder, a tool for constructing non-chimeric transcripts from read data that has been sequenced from sources containing isoform complexity.

resultsWe validated VTBuilder using reads simulated from 54 Sanger sequenced transcripts (SSTs) expressed in the venom gland of the saw scaled viper, Echis ocellatus. The SSTs were selected to represent genes from major co-expressed toxin groups known to harbor isoform variants. From the simulated reads, VTBuilder constructed 55 transcripts, 50 of which had a greater than 99% sequence similarity to 48 of the SSTs. In contrast, using the popular assembler tool Trinity (r2013-02-25), only 14 transcripts were constructed with a similar level of sequence identity to just 11 SSTs. Furthermore VTBuilder produced transcripts with a similar length distribution to the SSTs while those produced by Trinity were considerably shorter. To demonstrate that our approach can be scaled to real world data we assembled the venom gland transcriptome of the African puff adder Bitis arietans using paired-end reads sequenced on Illumina's MiSeq platform. VTBuilder constructed 1481 transcripts from 5 million reads and, following annotation, all major toxin genes were recovered demonstrating reconstruction of complex underlying sequence and isoform diversity.

conclusionUnlike other approaches, VTBuilder strives to maintain the relationships between co-evolving sites within the constructed transcripts, and thus increases transcript utility for a wide range of research areas ranging from transcriptomics to phylogenetics and including the monitoring of drug resistant parasite populations. Additionally, improving the quality of transcripts assembled from read data will have an impact on future studies that query these data. VTBuilder has been implemented in java and is available, under the GPL GPU V0.3 license, from http:// http://www.lstmed.ac.uk/vtbuilder .

Indexed as

High-Throughput Nucleotide SequencingSoftwareAnimalsComputational BiologyDatabases, FactualMolecular Sequence AnnotationProtein IsoformsTranscriptomeViperidaeViper VenomsProtein IsoformsViper Venoms

Identifiers

PMID25465054
PMCPMC4260244

What OpenQuestion holds

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LicenceCC BY
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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.