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Genome-wide patterns of copy number variation in the diversified chicken genomes using next-generation sequencing
BACKGROUND: Copy number variation (CNV) is important and widespread in the genome, and is a major cause of disease and phenotypic diversity. Herein, we performed a genome-wide CNV analysis in 12 diversified chicken genomes based on whole genome sequencing. RESULTS: A total of 8,840 CNV regions (CNVR...
Tallennettuna:
| Julkaisussa: | BMC Genomics |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4239369/ https://ncbi.nlm.nih.gov/pubmed/25378104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-962 |
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