Evidence map›Paper›PMID 35438138›Full record

ArticleBriefings in bioinformatics2022

A quality control portal for sequencing data deposited at the European genome-phenome archive.

Dietmar Fernández-Orth, Manuel Rueda, Babita Singh, Mauricio Moldes, Aina Jene, Marta Ferri, Claudia Vasallo, Lauren A Fromont, Arcadi Navarro, Jordi Rambla

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

10 authors.

Dietmar Fernández-OrthEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Manuel RuedaEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Babita SinghEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Mauricio MoldesEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Aina JeneEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Marta FerriEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Claudia VasalloEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Lauren A FromontEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Arcadi NavarroEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.
Jordi RamblaEuropean Genome-phenome Archive (EGA) in the Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology Dr. Aiguader 88, Barcelona, 08003 Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since its launch in 2008, the European Genome-Phenome Archive (EGA) has been leading the archiving and distribution of human identifiable genomic data. In this regard, one of the community concerns is the potential usability of the stored data, as of now, data submitters are not mandated to perform any quality control (QC) before uploading their data and associated metadata information. Here, we present a new File QC Portal developed at EGA, along with QC reports performed and created for 1 694 442 files [Fastq, sequence alignment map (SAM)/binary alignment map (BAM)/CRAM and variant call format (VCF)] submitted at EGA. QC reports allow anonymous EGA users to view summary-level information regarding the files within a specific dataset, such as quality of reads, alignment quality, number and type of variants and other features. Researchers benefit from being able to assess the quality of data prior to the data access decision and thereby, increasing the reusability of data (https://ega-archive.org/blog/data-upcycling-powered-by-ega/).

Indexed as

GenomeGenomicsHigh-Throughput Nucleotide SequencingHumansMetadataQuality ControlSoftwarebinary alignment map (BAM)European Genome-Phenome Archive (EGA)Fastqquality controlvariant call format (VCF)

Identifiers

PMID35438138
PMCPMC9116225

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.