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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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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6842140/ https://ncbi.nlm.nih.gov/pubmed/31703556 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-3182-x |
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