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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2010
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2875995/
https://ncbi.nlm.nih.gov/pubmed/20440878
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk