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Genome assembly comparison identifies structural variants in the human genome
Numerous types of DNA variation exist, ranging from SNPs to larger structural alterations such as copy number variants (CNVs) and inversions. Alignment of DNA sequence from different sources has been used to identify SNPs1,2 and intermediate-sized variants (ISVs)3. However, only a small proportion o...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2006
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2674632/ https://ncbi.nlm.nih.gov/pubmed/17115057 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng1921 |
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