Evidence map›Paper›PMID 34462322›Full record

ArticleLife science alliance2021

Statistical guidelines for quality control of next-generation sequencing techniques.

Maximilian Sprang, Matteo Krüger, Miguel A Andrade-Navarro, Jean-Fred Fontaine

Abstract read
In one paragraph

Article in Life science alliance, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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.

Maximilian SprangFaculty of Biology, Johannes Gutenberg-Universität Mainz, Biozentrum I, Mainz, Germany.ORCID 0000-0002-8438-4747
Matteo KrügerFaculty of Biology, Johannes Gutenberg-Universität Mainz, Biozentrum I, Mainz, Germany.
Miguel A Andrade-NavarroFaculty of Biology, Johannes Gutenberg-Universität Mainz, Biozentrum I, Mainz, Germany.ORCID 0000-0001-6650-1711
Jean-Fred FontaineFaculty of Biology, Johannes Gutenberg-Universität Mainz, Biozentrum I, Mainz, Germany fontaine@uni-mainz.de.ORCID 0000-0002-1101-4091

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More and more next-generation sequencing (NGS) data are made available every day. However, the quality of this data is not always guaranteed. Available quality control tools require profound knowledge to correctly interpret the multiplicity of quality features. Moreover, it is usually difficult to know if quality features are relevant in all experimental conditions. Therefore, the NGS community would highly benefit from condition-specific data-driven guidelines derived from many publicly available experiments, which reflect routinely generated NGS data. In this work, we have characterized well-known quality guidelines and related features in big datasets and concluded that they are too limited for assessing the quality of a given NGS file accurately. Therefore, we present new data-driven guidelines derived from the statistical analysis of many public datasets using quality features calculated by common bioinformatics tools. Thanks to this approach, we confirm the high relevance of genome mapping statistics to assess the quality of the data, and we demonstrate the limited scope of some quality features that are not relevant in all conditions. Our guidelines are available at https://cbdm.uni-mainz.de/ngs-guidelines.

Indexed as

Computational BiologyGenome, HumanHigh-Throughput Nucleotide SequencingHumansQuality ControlSequence Analysis, DNASoftware

Identifiers

PMID34462322
PMCPMC8408346

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.