Evidence map›Paper›PMID 28011720›Full record

ArticleDNA research : an international journal for rapid publication of reports on genes and genomes2017

Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP.

Valentino Ruggieri, Irantzu Anzar, Andreu Paytuvi, Roberta Calafiore, Riccardo Aiese Cigliano, Walter Sanseverino, Amalia Barone

Abstract readValidation Study
In one paragraph

Article in DNA research : an international journal for rapid publication of reports on genes and genomes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

7 authors.

Valentino RuggieriDepartment of Agricultural Sciences, University of Naples Federico II, Via Università 100, 80055 Portici (NA), Italy.
Irantzu AnzarSequentia Biotech SL, Calle Compte d'Urgell, 240, 08035 Barcelona, Spain.
Andreu PaytuviSequentia Biotech SL, Calle Compte d'Urgell, 240, 08035 Barcelona, Spain.
Roberta CalafioreDepartment of Agricultural Sciences, University of Naples Federico II, Via Università 100, 80055 Portici (NA), Italy.
Riccardo Aiese CiglianoSequentia Biotech SL, Calle Compte d'Urgell, 240, 08035 Barcelona, Spain.
Walter SanseverinoSequentia Biotech SL, Calle Compte d'Urgell, 240, 08035 Barcelona, Spain.
Amalia BaroneDepartment of Agricultural Sciences, University of Naples Federico II, Via Università 100, 80055 Portici (NA), Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent development of Sequence Capture methodology represents a powerful strategy for enhancing data generation to assess genetic variation of targeted genomic regions. Here, we present SUPER-CAP, a bioinformatics web tool aimed at handling Sequence Capture data, fine calculating the allele frequency of variations and building genotype-specific sequence of captured genes. The dataset used to develop this in silico strategy consists of 378 loci and related regulative regions in a collection of 44 tomato landraces. About 14,000 high-quality variants were identified. The high depth (>40×) of coverage and adopting the correct filtering criteria allowed identification of about 4,000 rare variants and 10 genes with a different copy number variation. We also show that the tool is capable to reconstruct genotype-specific sequences for each genotype by using the detected variants. This allows evaluating the combined effect of multiple variants in the same protein. The architecture and functionality of SUPER-CAP makes the software appropriate for a broad set of analyses including SNP discovery and mining. Its functionality, together with the capability to process large data sets and efficient detection of sequence variation, makes SUPER-CAP a valuable bioinformatics tool for genomics and breeding purposes.

Indexed as

Data MiningGene FrequencyGenes, PlantPolymorphism, Single NucleotideSequence AnalysisSolanum lycopersicumheterozygous variantssequence reconstructiontarget enrichmentweb tool analysis

Identifiers

PMID28011720
PMCPMC5381350

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.