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Mapping copy number variation by population scale genome sequencing
Genomic structural variants (SVs) are abundant in humans, differing from other variation classes in extent, origin, and functional impact. Despite progress in SV characterization, the nucleotide resolution architecture of most SVs remains unknown. We constructed a map of unbalanced SVs (i.e., copy n...
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3077050/ https://ncbi.nlm.nih.gov/pubmed/21293372 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature09708 |
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