-
1
-
-
23644449057
-
Direct genomic selection
-
Bashiardes S, Veile R, Helms C, Mardis ER, Bowcock AM, Lovett M: Direct genomic selection. Nat Methods 2005; 2: 63-69.
-
(2005)
Nat Methods
, vol.2
, pp. 63-69
-
-
Bashiardes, S.1
Veile, R.2
Helms, C.3
Mardis, E.R.4
Bowcock, A.M.5
Lovett, M.6
-
2
-
-
35748951614
-
Direct selection of human genomic loci by microarray hybridization
-
Albert TJ, Molla MN, Muzny DM et al: Direct selection of human genomic loci by microarray hybridization. Nat Methods 2007; 4: 903-905.
-
(2007)
Nat Methods
, vol.4
, pp. 903-905
-
-
Albert, T.J.1
Molla, M.N.2
Muzny, D.M.3
-
3
-
-
36549021060
-
Genome-wide in situ exon capture for selective resequencing
-
Hodges E, Xuan Z, Balija V et al: Genome-wide in situ exon capture for selective resequencing. Nat Genet 2007; 39: 1522-1527.
-
(2007)
Nat Genet
, vol.39
, pp. 1522-1527
-
-
Hodges, E.1
Xuan, Z.2
Balija, V.3
-
4
-
-
35748959649
-
Microarray-based genomic selection for high-throughput resequencing
-
Okou DT, Steinberg KM, Middle C, Cutler DJ, Albert TJ, Zwick ME: Microarray-based genomic selection for high-throughput resequencing. Nat Methods 2007; 4: 907-909.
-
(2007)
Nat Methods
, vol.4
, pp. 907-909
-
-
Okou, D.T.1
Steinberg, K.M.2
Middle, C.3
Cutler, D.J.4
Albert, T.J.5
Zwick, M.E.6
-
5
-
-
35748953750
-
Multiplex amplification of large sets of human exons
-
Porreca GJ, Zhang K, Li JB et al: Multiplex amplification of large sets of human exons. Nat Methods 2007; 4: 931-936.
-
(2007)
Nat Methods
, vol.4
, pp. 931-936
-
-
Porreca, G.J.1
Zhang, K.2
Li, J.B.3
-
6
-
-
67649631522
-
Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection
-
Herman DS, Hovingh GK, Iartchouk O et al: Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection. Nat Methods 2009; 6: 507-510.
-
(2009)
Nat Methods
, vol.6
, pp. 507-510
-
-
Herman, D.S.1
Hovingh, G.K.2
Iartchouk, O.3
-
7
-
-
75549091892
-
New strategies and emerging technologies for massively parallel sequencing: Applications in medical research
-
Mardis ER: New strategies and emerging technologies for massively parallel sequencing: applications in medical research. Genome Med 2009; 1: 40.
-
(2009)
Genome Med
, vol.1
, pp. 40
-
-
Mardis, E.R.1
-
8
-
-
0037313185
-
Extensive allelic variation and ultrashort telomeres in senescent human cells
-
Baird DM, Rowson J, Wynford-Thomas D, Kipling D: Extensive allelic variation and ultrashort telomeres in senescent human cells. Nat Genet 2003; 33: 203-207.
-
(2003)
Nat Genet
, vol.33
, pp. 203-207
-
-
Baird, D.M.1
Rowson, J.2
Wynford-Thomas, D.3
Kipling, D.4
-
9
-
-
0035812845
-
The shortest telomere, not average telomere length, is critical for cell viability and chromosome stability
-
Hemann MT, Strong MA, Hao LY, Greider CW: The shortest telomere, not average telomere length, is critical for cell viability and chromosome stability. Cell 2001; 107: 67-77.
-
(2001)
Cell
, vol.107
, pp. 67-77
-
-
Hemann, M.T.1
Strong, M.A.2
Hao, L.Y.3
Greider, C.W.4
-
10
-
-
24344442909
-
Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication
-
Linardopoulou EV, Williams EM, Fan Y, Friedman C, Young JM, Trask BJ: Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication. Nature 2005; 437: 94-100.
-
(2005)
Nature
, vol.437
, pp. 94-100
-
-
Linardopoulou, E.V.1
Williams, E.M.2
Fan, Y.3
Friedman, C.4
Young, J.M.5
Trask, B.J.6
-
11
-
-
35348907287
-
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy
-
Lemmers RJ, Wohlgemuth M, van der Gaag KJ et al: Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy. Am J Hum Genet 2007; 81: 884-894.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 884-894
-
-
Lemmers, R.J.1
Wohlgemuth, M.2
Van Der Gaag, K.J.3
-
12
-
-
34250873404
-
Sequence finishing and mapping of Drosophila melanogaster heterochromatin
-
Hoskins RA, Carlson JW, Kennedy C et al: Sequence finishing and mapping of Drosophila melanogaster heterochromatin. Science 2007; 316: 1625-1628.
-
(2007)
Science
, vol.316
, pp. 1625-1628
-
-
Hoskins, R.A.1
Carlson, J.W.2
Kennedy, C.3
-
13
-
-
0029943141
-
Perturbation of nuclear architecture by longdistance chromosome interactions
-
Dernburg AF, Broman KW, Fung JC et al: Perturbation of nuclear architecture by longdistance chromosome interactions. Cell 1996; 85: 745-759.
-
(1996)
Cell
, vol.85
, pp. 745-759
-
-
Dernburg, A.F.1
Broman, K.W.2
Fung, J.C.3
-
14
-
-
40949101673
-
Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: Report of 2 new cases
-
Millington K, Hudnall SD, Northup J, Panova N, Velagaleti G: Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases. Exp Mol Pathol 2008; 84: 189-193.
-
(2008)
Exp Mol Pathol
, vol.84
, pp. 189-193
-
-
Millington, K.1
Hudnall, S.D.2
Northup, J.3
Panova, N.4
Velagaleti, G.5
-
15
-
-
33748805480
-
Spreading of silent chromatin: Inaction at a distance
-
Talbert PB, Henikoff S: Spreading of silent chromatin: inaction at a distance. Nat Rev Genet 2006; 7: 793-803.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 793-803
-
-
Talbert, P.B.1
Henikoff, S.2
-
16
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A et al: A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007; 316: 1491-1493.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
-
17
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS et al: Genomewide association analysis of coronary artery disease. N Engl J Med 2007; 357: 443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
-
18
-
-
10744222767
-
Autosomal-dominant hypertension with type e brachydactyly is caused by rearrangement on the short arm of chromosome 12
-
Bahring S, Rauch A, Toka O et al: Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12. Hypertension 2004; 43: 471-476.
-
(2004)
Hypertension
, vol.43
, pp. 471-476
-
-
Bahring, S.1
Rauch, A.2
Toka, O.3
-
19
-
-
34447515727
-
Developmentally regulated activation of a SINE B2 repeat as a domain boundary in organogenesis
-
Lunyak VV, Prefontaine GG, Nunez E et al: Developmentally regulated activation of a SINE B2 repeat as a domain boundary in organogenesis. Science 2007; 317: 248-251.
-
(2007)
Science
, vol.317
, pp. 248-251
-
-
Lunyak, V.V.1
Prefontaine, G.G.2
Nunez, E.3
-
20
-
-
0141618451
-
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome
-
Varon R, Gooding R, Steglich C et al: Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome. Nat Genet 2003; 35: 185-189.
-
(2003)
Nat Genet
, vol.35
, pp. 185-189
-
-
Varon, R.1
Gooding, R.2
Steglich, C.3
-
21
-
-
33947581390
-
The impact of translocations and gene fusions on cancer causation
-
Mitelman F, Johansson B, Mertens F: The impact of translocations and gene fusions on cancer causation. Nat Rev Cancer 2007; 7: 233-245.
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 233-245
-
-
Mitelman, F.1
Johansson, B.2
Mertens, F.3
-
22
-
-
34547642493
-
Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer
-
Tomlins SA, Laxman B, Dhanasekaran SM et al: Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer. Nature 2007; 448: 595-599.
-
(2007)
Nature
, vol.448
, pp. 595-599
-
-
Tomlins, S.A.1
Laxman, B.2
Dhanasekaran, S.M.3
-
23
-
-
44349191457
-
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
-
Campbell PJ, Stephens PJ, Pleasance ED et al: Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet 2008; 40: 722-729.
-
(2008)
Nat Genet
, vol.40
, pp. 722-729
-
-
Campbell, P.J.1
Stephens, P.J.2
Pleasance, E.D.3
-
24
-
-
42349115184
-
Molecular definition of high resolution multicolor banding (MCB) probes: First within the human dna-sequence anchored fish-banding probe set
-
Weise A, Mrasek K, Fickelscher I et al: Molecular definition of high resolution multicolor banding (MCB) probes: first within the human dna-sequence anchored fish-banding probe set. J Histochem Cytochem 2008; 56: 487-493.
-
(2008)
J Histochem Cytochem
, vol.56
, pp. 487-493
-
-
Weise, A.1
Mrasek, K.2
Fickelscher, I.3
-
25
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
-
Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A: Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 1992; 13: 718-725.
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.E.3
Nordenskjold, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
26
-
-
0036044083
-
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries
-
Liehr T, Weise A, Heller A et al: Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenet Genome Res 2002; 97: 43-50.
-
(2002)
Cytogenet Genome Res
, vol.97
, pp. 43-50
-
-
Liehr, T.1
Weise, A.2
Heller, A.3
-
27
-
-
42249087308
-
The complete genome of an individual by massively parallel DNA sequencing
-
Wheeler DA, Srinivasan M, Egholm M et al: The complete genome of an individual by massively parallel DNA sequencing. Nature 2008; 452: 872-876.
-
(2008)
Nature
, vol.452
, pp. 872-876
-
-
Wheeler, D.A.1
Srinivasan, M.2
Egholm, M.3
-
28
-
-
65449144325
-
Evaluation of next generation sequencing platforms for population targeted sequencing studies
-
Harismendy O, Ng PC, Strausberg RL et al: Evaluation of next generation sequencing platforms for population targeted sequencing studies. Genome Biol 2009; 10: R32.
-
(2009)
Genome Biol
, vol.10
-
-
Harismendy, O.1
Ng, P.C.2
Strausberg, R.L.3
-
29
-
-
36249021315
-
Genome-wide experimental determination of barriers to horizontal gene transfer
-
Sorek R, Zhu Y, Creevey CJ, Francino MP, Bork P, Rubin EM: Genome-wide experimental determination of barriers to horizontal gene transfer. Science 2007; 318: 1449-1452.
-
(2007)
Science
, vol.318
, pp. 1449-1452
-
-
Sorek, R.1
Zhu, Y.2
Creevey, C.J.3
Francino, M.P.4
Bork, P.5
Rubin, E.M.6
-
30
-
-
0029657886
-
Localization of chi1-related helicase genes to human chromosome regions 12p11 and 12p13: Similarity between parts of these genes and conserved human telomeric-associated DNA
-
Amann J, Valentine M, Kidd VJ, Lahti JM: Localization of chi1-related helicase genes to human chromosome regions 12p11 and 12p13: similarity between parts of these genes and conserved human telomeric-associated DNA. Genomics 1996; 32: 260-265.
-
(1996)
Genomics
, vol.32
, pp. 260-265
-
-
Amann, J.1
Valentine, M.2
Kidd, V.J.3
Lahti, J.M.4
-
31
-
-
0037047628
-
Recent segmental duplications in the human genome
-
Bailey JA, Gu Z, Clark RA et al: Recent segmental duplications in the human genome. Science 2002; 297: 1003-1007.
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
Gu, Z.2
Clark, R.A.3
-
32
-
-
0027284770
-
Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse
-
Lundin LG: Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse. Genomics 1993; 16: 1-19.
-
(1993)
Genomics
, vol.16
, pp. 1-19
-
-
Lundin, L.G.1
-
33
-
-
10344222632
-
Patterns of segmental duplication in the human genome
-
Zhang L, Lu HH, Chung WY, Yang J, Li WH: Patterns of segmental duplication in the human genome. Mol Biol Evol 2005; 22: 135-141.
-
(2005)
Mol Biol Evol
, vol.22
, pp. 135-141
-
-
Zhang, L.1
Lu, H.H.2
Chung, W.Y.3
Yang, J.4
Li, W.H.5
|