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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  The combined analysis as the best strategy for Dual RNA-Seq mapping
Autores:  Espindula,Eliandro
Sperb,Edilena Reis
Bach,Evelise
Passaglia,Luciane Maria Pereira
Data:  2019-01-01
Ano:  2019
Palavras-chave:  Dual RNA-Seq
Sequential analysis
Combined analysis
Mapping strategies
Resumo:  Abstract In Dual RNA-Seq experiments the simultaneous extraction of RNA and analysis of gene expression data from both interacting organisms could be a challenge. One alternative is separating the reads during in silico data analysis. There are two main mapping methods used: sequential and combined. Here we present a combined approach in which the libraries were aligned to a concatenated genome to sort the reads before mapping them to the respective annotated genomes. A comparison of this method with the sequential analysis was performed. Two RNA-Seq libraries available in public databases consisting of a eukaryotic (Zea mays) and a prokaryotic (Herbaspirillum seropediceae) organisms were mixed to simulate a Dual RNA-Seq experiment. Libraries from real Dual RNA-Seq experiments were also used. The sequential analysis consistently attributed more reads to the first reference genome used in the analysis (due to cross-mapping) than the combined approach. More importantly, the combined analysis resulted in lower numbers of cross-mapped reads. Our results highlight the necessity of combining the reference genomes to sort reads previously to the counting step to avoid losing information in Dual RNA-Seq experiments. Since most studies first map the RNA-Seq libraries to the eukaryotic genome, much prokaryotic information has probably been lost.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000500803
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/1678-4685-gmb-2019-0215
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.42 n.4 2019
Direitos:  info:eu-repo/semantics/openAccess
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