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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...

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書目詳細資料
Main Authors: Bashir, Ali, Bansal, Vikas, Bafna, Vineet
格式: Artigo
語言:Inglês
出版: BioMed Central 2010
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3091630/
https://ncbi.nlm.nih.gov/pubmed/20565853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-11-385
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