Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data

Schilbert H, Rempel A, Pucker B (2020)
Plants 9(4): 439.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Abstract / Bemerkung
High-throughput sequencing technologies have rapidly developed during the past years and have become an essential tool in plant sciences. However, the analysis of genomic data remains challenging and relies mostly on the performance of automatic pipelines. Frequently applied pipelines involve the alignment of sequence reads against a reference sequence and the identification of sequence variants. Since most benchmarking studies of bioinformatics tools for this purpose have been conducted on human datasets, there is a lack of benchmarking studies in plant sciences. In this study, we evaluated the performance of 50 different variant calling pipelines, including five read mappers and ten variant callers, on six real plant datasets of the model organism Arabidopsis thaliana. Sets of variants were evaluated based on various parameters including sensitivity and specificity. We found that all investigated tools are suitable for analysis of NGS data in plant research. When looking at different performance metrics, BWA-MEM and Novoalign were the best mappers and GATK returned the best results in the variant calling step
Stichworte
Single Nucleotide Variants (SNVs); Single Nucleotide Polymorphisms (SNPs); Insertions/Deletions (InDels); population genomics; re-sequencing; mapper; benchmarking; Next Generation Sequencing (NGS); bioinformatics; plant genomics
Erscheinungsjahr
2020
Zeitschriftentitel
Plants
Band
9
Ausgabe
4
Art.-Nr.
439
eISSN
2223-7747
Finanzierungs-Informationen
Open-Access-Publikationskosten wurden durch die Deutsche Forschungsgemeinschaft und die Universität Bielefeld gefördert.
Page URI
https://pub.uni-bielefeld.de/record/2942341

Zitieren

Schilbert H, Rempel A, Pucker B. Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data. Plants. 2020;9(4): 439.
Schilbert, H., Rempel, A., & Pucker, B. (2020). Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data. Plants, 9(4), 439. doi:10.3390/plants9040439
Schilbert, Hanna, Rempel, Andreas, and Pucker, Boas. 2020. “Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data”. Plants 9 (4): 439.
Schilbert, H., Rempel, A., and Pucker, B. (2020). Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data. Plants 9:439.
Schilbert, H., Rempel, A., & Pucker, B., 2020. Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data. Plants, 9(4): 439.
H. Schilbert, A. Rempel, and B. Pucker, “Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data”, Plants, vol. 9, 2020, : 439.
Schilbert, H., Rempel, A., Pucker, B.: Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data. Plants. 9, : 439 (2020).
Schilbert, Hanna, Rempel, Andreas, and Pucker, Boas. “Comparison of Read Mapping and Variant Calling Tools for the Analysis of Plant NGS Data”. Plants 9.4 (2020): 439.
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Gold standard of Nd1 vs TAIR10 sequence variants
Schilbert H, Rempel A, Pucker B (2020)
Bielefeld University.
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PMID: 32252268
PubMed | Europe PMC

Preprint: 10.1101/2020.03.10.986059

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