ロード中...
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...
保存先:
| 主要な著者: | , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2010
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|