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Detecting and correcting systematic variation in large-scale RNA sequencing data
High-throughput RNA sequencing (RNA-seq) enables comprehensive scans of entire transcriptomes, but best practices for analyzing RNA-seq data have not been fully defined, particularly for data collected with multiple sequencing platforms or at multiple sites. Here we used standardized RNA samples wit...
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| Main Authors: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4160374/ https://ncbi.nlm.nih.gov/pubmed/25150837 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nbt.3000 |
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