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Haplotype sorting using human fosmid clone end-sequence pairs
An important goal of human genetics and genomics is to understand the complete spectrum of genetic variation across a specific human haplotype. By combining information from a dense SNP map with fosmid end-sequence pairs (ESPs) aligned to the human genome reference sequence, we have developed a simp...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2593576/ https://ncbi.nlm.nih.gov/pubmed/18836033 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.081786.108 |
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