ロード中...
Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins
BACKGROUND: Copy number variations (CNVs) are widespread in the human or animal genome and are a significant source of genetic variation, which has been demonstrated to play an important role in phenotypic diversity. Advances in technology have allowed for identification of a large number of CNVs in...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2013
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3639935/ https://ncbi.nlm.nih.gov/pubmed/23442346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-131 |
| 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!
|