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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 3 |
2024 | 0 |
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5 results
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Page 1
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.
Personalized copy number and segmental duplication maps using next-generation sequencing.
Alkan C, Kidd JM, Marques-Bonet T, Aksay G, Antonacci F, Hormozdiari F, Kitzman JO, Baker C, Malig M, Mutlu O, Sahinalp SC, Gibbs RA, Eichler EE.
Alkan C, et al.
Nat Genet. 2009 Oct;41(10):1061-7. doi: 10.1038/ng.437. Epub 2009 Aug 30.
Nat Genet. 2009.
PMID: 19718026
Free PMC article.
Item in Clipboard
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.
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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Diversity of human copy number variation and multicopy genes.
Sudmant PH, Kitzman JO, Antonacci F, Alkan C, Malig M, Tsalenko A, Sampas N, Bruhn L, Shendure J; 1000 Genomes Project; Eichler EE.
Sudmant PH, et al.
Science. 2010 Oct 29;330(6004):641-6. doi: 10.1126/science.1197005.
Science. 2010.
PMID: 21030649
Free PMC article.
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Systematic assessment of copy number variant detection via genome-wide SNP genotyping.
Cooper GM, Zerr T, Kidd JM, Eichler EE, Nickerson DA.
Cooper GM, et al.
Nat Genet. 2008 Oct;40(10):1199-203. doi: 10.1038/ng.236. Epub 2008 Sep 7.
Nat Genet. 2008.
PMID: 18776910
Free PMC article.
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