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...

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Detalles Bibliográficos
Autores principales: Bashir, Ali, Bansal, Vikas, Bafna, Vineet
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Methodology Article
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

Internet

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

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