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Designing deep sequencing experiments: detecting structural variation and estimating transcript abundance
BACKGROUND: Massively parallel DNA sequencing technologies have enabled the sequencing of several individual human genomes. These technologies are also being used in novel ways for mRNA expression profiling, genome-wide discovery of transcription-factor binding sites, small RNA discovery, etc. The m...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091630/ https://www.ncbi.nlm.nih.gov/pubmed/20565853 http://dx.doi.org/10.1186/1471-2164-11-385 |