ロード中...
FLAGS, frequently mutated genes in public exomes
BACKGROUND: Dramatic improvements in DNA-sequencing technologies and computational analyses have led to wide use of whole exome sequencing (WES) to identify the genetic basis of Mendelian disorders. More than 180 novel rare-disease-causing genes with Mendelian inheritance patterns have been discover...
保存先:
| 出版年: | BMC Med Genomics |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2014
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4267152/ https://ncbi.nlm.nih.gov/pubmed/25466818 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-014-0064-y |
| 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!
|