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Massive screening of copy number population-scale variation in Bos taurus genome
BACKGROUND: Copy number variations (CNVs) represent a significant source of genomic structural variation. Their length ranges from approximately one hundred to millions of base pair. Genome-wide screenings have clarified that CNVs are a ubiquitous phenomenon affecting essentially the whole genome. A...
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| Autori principali: | , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3618309/ https://ncbi.nlm.nih.gov/pubmed/23442185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-124 |
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