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A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection
BACKGROUND: The application of high-throughput sequencing in a broad range of quantitative genomic assays (e.g., DNA-seq, ChIP-seq) has created a high demand for the analysis of large-scale read-count data. Typically, the genome is divided into tiling windows and windowed read-count data is generate...
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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5831535/ https://ncbi.nlm.nih.gov/pubmed/29490610 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2077-6 |
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