One is not enough: On the effects of reference genome for the mapping and subsequent analyses of short-reads

Carlos Valiente-Mullor, Beatriz Beamud, Ivan Ansari, Carlos Frances-Cuesta, Neris Garcia-Gonzalez, Lorena Mejia, Paula Ruiz-Hueso, Fernando Gonzalez-Candelas

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

29 Citas (Scopus)


Mapping of high-throughput sequencing (HTS) reads to a single arbitrary reference genome is a frequently used approach in microbial genomics. However, the choice of a reference may represent a source of errors that may affect subsequent analyses such as the detection of single nucleotide polymorphisms (SNPs) and phylogenetic inference. In this work, we evaluated the effect of reference choice on short-read sequence data from five clinically and epidemiologically relevant bacteria (Klebsiella pneumoniae, Legionella pneumophila, Neisseria gonorrhoeae, Pseudomonas aeruginosa and Serratia marcescens). Publicly available whole-genome assemblies encompassing the genomic diversity of these species were selected as reference sequences, and read alignment statistics, SNP calling, recombination rates, dN/dS ratios, and phylogenetic trees were evaluated depending on the mapping reference. The choice of different reference genomes proved to have an impact on almost all the parameters considered in the five species. In addition, these biases had potential epidemiological implications such as including/excluding isolates of particular clades and the estimation of genetic distances. These findings suggest that the single reference approach might introduce systematic errors during mapping that affect subsequent analyses, particularly for data sets with isolates from genetically diverse backgrounds. In any case, exploring the effects of different references on the final conclusions is highly recommended.

Idioma originalInglés
Número de artículoe1008678
PublicaciónPLoS Computational Biology
EstadoPublicada - 27 ene. 2021


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