Detalhe da pesquisa
1.
A human genome structural variation sequencing resource reveals insights into mutational mechanisms.
Cell
; 143(5): 837-47, 2010 Nov 24.
Artigo
Inglês
| MEDLINE | ID: mdl-21111241
2.
Characterization of missing human genome sequences and copy-number polymorphic insertions.
Nat Methods
; 7(5): 365-71, 2010 May.
Artigo
Inglês
| MEDLINE | ID: mdl-20440878