-
1
-
-
84877097089
-
Potential of whole-genome sequencing for determining risk and personalizing therapy: Focus on AML
-
Borate U, Absher D, Erba HP, Pasche B (2012) Potential of whole-genome sequencing for determining risk and personalizing therapy: focus on AML. Expert Rev Anticancer Ther 12:1289-1297.
-
(2012)
Expert Rev Anticancer Ther
, vol.12
, pp. 1289-1297
-
-
Borate, U.1
Absher, D.2
Erba, H.P.3
Pasche, B.4
-
2
-
-
84863457092
-
What is personalized medicine and what should it replace?
-
Whitcomb DC (2012) What is personalized medicine and what should it replace? Nat Rev Gastroenterol Hepatol 9:418-424.
-
(2012)
Nat Rev Gastroenterol Hepatol
, vol.9
, pp. 418-424
-
-
Whitcomb, D.C.1
-
3
-
-
84555187724
-
Targeted enrichment of genomic DNA regions for next-generation sequencing
-
Mertes F, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, et al. (2011) Targeted enrichment of genomic DNA regions for next-generation sequencing. Brief Funct Genomics 10:374-386.
-
(2011)
Brief Funct Genomics
, vol.10
, pp. 374-386
-
-
Mertes, F.1
Elsharawy, A.2
Sauer, S.3
Van Helvoort, J.M.4
Van Der Zaag, P.J.5
-
4
-
-
84888297585
-
Application of whole exome sequencing to identify disease-causing variants in inherited human diseases
-
Goh G, Choi M (2012) Application of whole exome sequencing to identify disease-causing variants in inherited human diseases. Genomics Inform 10:214-219.
-
(2012)
Genomics Inform
, vol.10
, pp. 214-219
-
-
Goh, G.1
Choi, M.2
-
5
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke A, Melnikov A, Maguire J, Rogov P, LeProust EM, et al. (2009) Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat Biotechnol 27:182-189.
-
(2009)
Nat Biotechnol
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
Melnikov, A.2
Maguire, J.3
Rogov, P.4
LeProust, E.M.5
-
6
-
-
80054757012
-
Performance comparison of exome DNA sequencing technologies
-
Clark MJ, Chen R, Lam HY, Karczewski KJ, Euskirchen G, et al. (2011) Performance comparison of exome DNA sequencing technologies. Nat Biotechnol 29:908-914.
-
(2011)
Nat Biotechnol
, vol.29
, pp. 908-914
-
-
Clark, M.J.1
Chen, R.2
Lam, H.Y.3
Karczewski, K.J.4
Euskirchen, G.5
-
7
-
-
59149084538
-
The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores
-
Irizarry RA, Ladd-Acosta C, Wen B, Wu Z, Montano C, et al. (2009) The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores. Nat Genet 41:178-186.
-
(2009)
Nat Genet
, vol.41
, pp. 178-186
-
-
Irizarry, R.A.1
Ladd-Acosta, C.2
Wen, B.3
Wu, Z.4
Montano, C.5
-
8
-
-
85027954125
-
DNA methylation profiling in the clinic: Applications and challenges
-
Heyn H, Esteller M (2012) DNA methylation profiling in the clinic: applications and challenges. Nat Rev Genet 13:679-692.
-
(2012)
Nat Rev Genet
, vol.13
, pp. 679-692
-
-
Heyn, H.1
Esteller, M.2
-
9
-
-
84875864497
-
Wholegenome haplotyping by dilution, amplification, and sequencing
-
Kaper F, Swamy S, Klotzle B, Munchel S, Cottrell J, et al. (2013) Wholegenome haplotyping by dilution, amplification, and sequencing. Proc Natl Acad Sci U S A 110:5552-5557.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 5552-5557
-
-
Kaper, F.1
Swamy, S.2
Klotzle, B.3
Munchel, S.4
Cottrell, J.5
-
10
-
-
35748953750
-
Multiplex amplification of large sets of human exons
-
Porreca GJ, Zhang K, Li JB, Xie B, Austin D, et al. (2007) Multiplex amplification of large sets of human exons. Nat Methods 4:931-936.
-
(2007)
Nat Methods
, vol.4
, pp. 931-936
-
-
Porreca, G.J.1
Zhang, K.2
Li, J.B.3
Xie, B.4
Austin, D.5
-
11
-
-
79551469517
-
Targeted resequencing of candidate genes using selector probes
-
Johansson H, Isaksson M, Sorqvist EF, Roos F, Stenberg J, et al. (2011) Targeted resequencing of candidate genes using selector probes. Nucleic Acids Res 39:e8.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. e8
-
-
Johansson, H.1
Isaksson, M.2
Sorqvist, E.F.3
Roos, F.4
Stenberg, J.5
-
12
-
-
84857784165
-
Library-free methylation sequencing with bisulfite padlock probes
-
Diep D, Plongthongkum N, Gore A, Fung HL, Shoemaker R, et al. (2012) Library-free methylation sequencing with bisulfite padlock probes. Nat Methods 9:270-272.
-
(2012)
Nat Methods
, vol.9
, pp. 270-272
-
-
Diep, D.1
Plongthongkum, N.2
Gore, A.3
Fung, H.L.4
Shoemaker, R.5
-
13
-
-
55549092780
-
Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes
-
Varley KE, Mitra RD (2008) Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes. Genome Res 18:1844-1850.
-
(2008)
Genome Res
, vol.18
, pp. 1844-1850
-
-
Varley, K.E.1
Mitra, R.D.2
-
14
-
-
0028820187
-
Solid-phase reversible immobilization for the isolation of PCR products
-
DeAngelis MM, Wang DG, Hawkins TL (1995) Solid-phase reversible immobilization for the isolation of PCR products. Nucleic Acids Res 23:4742-4743.
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 4742-4743
-
-
DeAngelis, M.M.1
Wang, D.G.2
Hawkins, T.L.3
-
15
-
-
84863101693
-
AdapterRemoval: Easy cleaning of next-generation sequencing reads
-
Lindgreen S (2012) AdapterRemoval: easy cleaning of next-generation sequencing reads. BMC Res Notes 5:337.
-
(2012)
BMC Res Notes
, vol.5
, pp. 337
-
-
Lindgreen, S.1
-
16
-
-
23644449057
-
Direct genomic selection
-
Bashiardes S, Veile R, Helms C, Mardis ER, Bowcock AM, et al. (2005) Direct genomic selection. Nat Methods 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
-
17
-
-
84876528012
-
High-resolution nucleosome mapping of targeted regions using BAC-based enrichment
-
Yigit E, Zhang Q, Xi L, Grilley D, Widom J, et al. (2013) High-resolution nucleosome mapping of targeted regions using BAC-based enrichment. Nucleic Acids Res 41:e87.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. e87
-
-
Yigit, E.1
Zhang, Q.2
Xi, L.3
Grilley, D.4
Widom, J.5
-
18
-
-
84890151805
-
Pulling out the 1%: Whole-genome capture for the targeted enrichment of ancient DNA sequencing libraries
-
Carpenter ML, Buenrostro JD, Valdiosera C, Schroeder H, Allentoft ME, et al. (2013) Pulling out the 1%: Whole-Genome Capture for the Targeted Enrichment of Ancient DNA Sequencing Libraries. The American Journal of Human Genetics 93:852-864.
-
(2013)
The American Journal of Human Genetics
, vol.93
, pp. 852-864
-
-
Carpenter, M.L.1
Buenrostro, J.D.2
Valdiosera, C.3
Schroeder, H.4
Allentoft, M.E.5
-
19
-
-
77950405093
-
Genome-wide association study of CNVs in 16, 000 cases of eight common diseases and 3, 000 shared controls
-
Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, et al. (2010) Genome-wide association study of CNVs in 16, 000 cases of eight common diseases and 3, 000 shared controls. Nature 464:713-720.
-
(2010)
Nature
, vol.464
, pp. 713-720
-
-
Craddock, N.1
Hurles, M.E.2
Cardin, N.3
Pearson, R.D.4
Plagnol, V.5
-
22
-
-
84871211606
-
How the leopard hides its spots: ASIP mutations and melanism in wild cats
-
Schneider A, David VA, Johnson WE, O'Brien SJ, Barsh GS, et al. (2012) How the leopard hides its spots: ASIP mutations and melanism in wild cats. PLoS One 7:e50386.
-
(2012)
PLoS One
, vol.7
, pp. e50386
-
-
Schneider, A.1
David, V.A.2
Johnson, W.E.3
O'Brien, S.J.4
Barsh, G.S.5
-
23
-
-
49649125042
-
Genomescale DNA methylation maps of pluripotent and differentiated cells
-
Meissner A, Mikkelsen TS, Gu H, Wernig M, Hanna J, et al. (2008) Genomescale DNA methylation maps of pluripotent and differentiated cells. Nature 454:766-770.
-
(2008)
Nature
, vol.454
, pp. 766-770
-
-
Meissner, A.1
Mikkelsen, T.S.2
Gu, H.3
Wernig, M.4
Hanna, J.5
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