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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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Bibliografske podrobnosti
Main Authors: Kidd, Jeffrey M., Cheng, Ze, Graves, Tina, Fulton, Bob, Wilson, Richard K., Eichler, Evan E.
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 2008
Teme:
Online dostop: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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