VARUS: sampling complementary RNA reads from the sequence read archive

BACKGROUND: Vast amounts of next generation sequencing RNA data has been deposited in archives, accompanying very diverse original studies. The data is readily available also for other purposes such as genome annotation or transcriptome assembly. However, selecting a subset of available experiments,...

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Detalles Bibliográficos
Autores principales: Stanke, Mario, Bruhn, Willy, Becker, Felix, Hoff, Katharina J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842140/
https://www.ncbi.nlm.nih.gov/pubmed/31703556
http://dx.doi.org/10.1186/s12859-019-3182-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842140/
https://www.ncbi.nlm.nih.gov/pubmed/31703556
http://dx.doi.org/10.1186/s12859-019-3182-x

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