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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 3 |
2007 | 3 |
2011 | 3 |
2024 | 0 |
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8 results
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Page 1
The population genetics of structural variation.
Nat Genet. 2007 Jul;39(7 Suppl):S30-6. doi: 10.1038/ng2042.
Nat Genet. 2007.
PMID: 17597779
Free PMC article.
Review.
Challenges and standards in integrating surveys of structural variation.
Scherer SW, Lee C, Birney E, Altshuler DM, Eichler EE, Carter NP, Hurles ME, Feuk L.
Scherer SW, et al.
Nat Genet. 2007 Jul;39(7 Suppl):S7-15. doi: 10.1038/ng2093.
Nat Genet. 2007.
PMID: 17597783
Free PMC article.
Review.
Item in Clipboard
Assaying chromosomal inversions by single-molecule haplotyping.
Turner DJ, Shendure J, Porreca G, Church G, Green P, Tyler-Smith C, Hurles ME.
Turner DJ, et al.
Nat Methods. 2006 Jun;3(6):439-45. doi: 10.1038/nmeth881.
Nat Methods. 2006.
PMID: 16721377
Free PMC article.
Item in Clipboard
Mapping copy number variation by population-scale genome sequencing.
Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C, Abyzov A, Yoon SC, Ye K, Cheetham RK, Chinwalla A, Conrad DF, Fu Y, Grubert F, Hajirasouliha I, Hormozdiari F, Iakoucheva LM, Iqbal Z, Kang S, Kidd JM, Konkel MK, Korn J, Khurana E, Kural D, Lam HY, Leng J, Li R, Li Y, Lin CY, Luo R, Mu XJ, Nemesh J, Peckham HE, Rausch T, Scally A, Shi X, Stromberg MP, Stütz AM, Urban AE, Walker JA, Wu J, Zhang Y, Zhang ZD, Batzer MA, Ding L, Marth GT, McVean G, Sebat J, Snyder M, Wang J, Ye K, Eichler EE, Gerstein MB, Hurles ME, Lee C, McCarroll SA, Korbel JO; 1000 Genomes Project.
Mills RE, et al.
Nature. 2011 Feb 3;470(7332):59-65. doi: 10.1038/nature09708.
Nature. 2011.
PMID: 21293372
Free PMC article.
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High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia.
Nik-Zainal S, Strick R, Storer M, Huang N, Rad R, Willatt L, Fitzgerald T, Martin V, Sandford R, Carter NP, Janecke AR, Renner SP, Oppelt PG, Oppelt P, Schulze C, Brucker S, Hurles M, Beckmann MW, Strissel PL, Shaw-Smith C.
Nik-Zainal S, et al.
J Med Genet. 2011 Mar;48(3):197-204. doi: 10.1136/jmg.2010.082412. Epub 2011 Jan 28.
J Med Genet. 2011.
PMID: 21278390
Free PMC article.
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Global variation in copy number in the human genome.
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, González JR, Gratacòs M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME.
Redon R, et al.
Nature. 2006 Nov 23;444(7118):444-54. doi: 10.1038/nature05329.
Nature. 2006.
PMID: 17122850
Free PMC article.
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Y chromosomal STRs haplotypes in two populations from Bolivia.
Lee J, Ewis AA, Hurles ME, Kashiwazaki H, Shinka T, Nakahori Y.
Lee J, et al.
Leg Med (Tokyo). 2007 Jan;9(1):43-7. doi: 10.1016/j.legalmed.2006.08.004. Epub 2006 Dec 5.
Leg Med (Tokyo). 2007.
PMID: 17150402
Free PMC article.
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Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.
Pinto D, Darvishi K, Shi X, Rajan D, Rigler D, Fitzgerald T, Lionel AC, Thiruvahindrapuram B, Macdonald JR, Mills R, Prasad A, Noonan K, Gribble S, Prigmore E, Donahoe PK, Smith RS, Park JH, Hurles ME, Carter NP, Lee C, Scherer SW, Feuk L.
Pinto D, et al.
Nat Biotechnol. 2011 May 8;29(6):512-20. doi: 10.1038/nbt.1852.
Nat Biotechnol. 2011.
PMID: 21552272
Free PMC article.
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