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Optimizing de novo assembly of short-read RNA-seq data for phylogenomics

BACKGROUND: RNA-seq has shown huge potential for phylogenomic inferences in non-model organisms. However, error, incompleteness, and redundant assembled transcripts for each gene in de novo assembly of short reads cause noise in analyses and a large amount of missing data in the aligned matrix. To a...

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Detalles Bibliográficos
Autores principales: Yang, Ya, Smith, Stephen A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663818/
https://www.ncbi.nlm.nih.gov/pubmed/23672450
http://dx.doi.org/10.1186/1471-2164-14-328

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