Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions

The extent of human genomic structural variation suggests that there must be portions of the genome yet to be discovered, annotated and characterized at the sequence level. We present a resource and analysis of 2,363 novel insertion sequences corresponding to 720 genomic loci. We show that a substan...

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Main Authors: Kidd, Jeffrey M., Sampas, Nick, Antonacci, Francesca, Graves, Tina, Fulton, Robert, Hayden, Hillary S., Alkan, Can, Malig, Maika, Ventura, Mario, Giannuzzi, Giuliana, Kallicki, Joelle, Anderson, Paige, Tsalenko, Anya, Yamada, N. Alice, Tsang, Peter, Kaul, Rajinder, Wilson, Richard K., Bruhn, Laurakay, Eichler, Evan E.
פורמט: Artigo
שפה:Inglês
יצא לאור: 2010
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Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC2875995/
https://ncbi.nlm.nih.gov/pubmed/20440878
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