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A human genome structural variation sequencing resource reveals insights into mutational mechanisms.
Cell. 2010 Nov 24;143(5):837-47. doi: 10.1016/j.cell.2010.10.027.
Cell. 2010.
PMID: 21111241
Free PMC article.
Characterization of missing human genome sequences and copy-number polymorphic insertions.
Kidd JM, Sampas N, Antonacci F, Graves T, Fulton R, Hayden HS, Alkan C, Malig M, Ventura M, Giannuzzi G, Kallicki J, Anderson P, Tsalenko A, Yamada NA, Tsang P, Kaul R, Wilson RK, Bruhn L, Eichler EE.
Kidd JM, et al. Among authors: kallicki j.
Nat Methods. 2010 May;7(5):365-71. doi: 10.1038/nmeth.1451.
Nat Methods. 2010.
PMID: 20440878
Free PMC article.
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