-
1
-
-
0025525784
-
-
Weber, J.L. Human DNA polymorphisms and methods of analysis. Curr. Opin. Biotechnol. 1990, 1, 166-71.
-
Weber, J.L. Human DNA polymorphisms and methods of analysis. Curr. Opin. Biotechnol. 1990, 1, 166-71.
-
-
-
-
2
-
-
26444577151
-
-
Tamiya, G.; Shinya, M.; Imanishi, T.; Ikuta, T.; Makino, S.; Okamoto, K.; Furugaki, K.; Matsumoto, T.; Mano, S.; Ando, S.; Nozaki, Y.; Yukawa, W.; Nakashige, R.; Yamaguchi, D.; Ishibashi, H.; Yonekura, M.; Nakami, Y.; Takayama, S.; Endo, T.; Saruwatari, T.; Yagura, M.; Yoshikawa, Y.; Fujimoto, K.; Oka, A.; Chiku, S.; Linsen, S.E.; Giphart, M.J.; Kulski, J.K.; Fukazawa, T.; Hashimoto, H.; Kimura, M.; Hoshina, Y.; Suzuki, Y.; Hotta, T.; Mochida, J.; Minezaki, T.; Komai, K.; Shiozawa, S.; Taniguchi, A.; Yamanaka, H.; Kamatani, N.; Gojobori, T.; Bahram, S.; Inoko, H. Whole genome association study of rheumatoid arthritis using 27 039 microsatellites. Hum. Mol. Genet. 2005, 14, 2305-21.
-
Tamiya, G.; Shinya, M.; Imanishi, T.; Ikuta, T.; Makino, S.; Okamoto, K.; Furugaki, K.; Matsumoto, T.; Mano, S.; Ando, S.; Nozaki, Y.; Yukawa, W.; Nakashige, R.; Yamaguchi, D.; Ishibashi, H.; Yonekura, M.; Nakami, Y.; Takayama, S.; Endo, T.; Saruwatari, T.; Yagura, M.; Yoshikawa, Y.; Fujimoto, K.; Oka, A.; Chiku, S.; Linsen, S.E.; Giphart, M.J.; Kulski, J.K.; Fukazawa, T.; Hashimoto, H.; Kimura, M.; Hoshina, Y.; Suzuki, Y.; Hotta, T.; Mochida, J.; Minezaki, T.; Komai, K.; Shiozawa, S.; Taniguchi, A.; Yamanaka, H.; Kamatani, N.; Gojobori, T.; Bahram, S.; Inoko, H. Whole genome association study of rheumatoid arthritis using 27 039 microsatellites. Hum. Mol. Genet. 2005, 14, 2305-21.
-
-
-
-
3
-
-
15444352074
-
-
Ghosh, S.; Karanjawala, Z.E.; Hauser, E.R.; Ally, D.; Knapp, J.I.; Rayman, J.B.; Musick, A.; Tannenbaum, J.; Te, C.; Shapiro, S.; Eldridge, W.; Musick, T.; Martin, C.; Smith, J.R.; Carpten, J.D.; Brownstein, M.J.; Powell, J.I.; Whiten, R.; Chines, P.; Nylund, S.J.; Magnuson, V.L.; Boehnke, M.; Collins, F.S. Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. Genome Res. 1997, 7, 165-78.
-
Ghosh, S.; Karanjawala, Z.E.; Hauser, E.R.; Ally, D.; Knapp, J.I.; Rayman, J.B.; Musick, A.; Tannenbaum, J.; Te, C.; Shapiro, S.; Eldridge, W.; Musick, T.; Martin, C.; Smith, J.R.; Carpten, J.D.; Brownstein, M.J.; Powell, J.I.; Whiten, R.; Chines, P.; Nylund, S.J.; Magnuson, V.L.; Boehnke, M.; Collins, F.S. Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. Genome Res. 1997, 7, 165-78.
-
-
-
-
4
-
-
34249323364
-
Linkage Mapping
-
John Wiley & Sons, Inc, New York
-
Samuels, M.E.; Dubé, M.P. Linkage Mapping. In Encyclopedia of Genetics, Genomics, Proteomics, and Bioinformatics; John Wiley & Sons, Inc.: New York, 2005.
-
(2005)
Encyclopedia of Genetics, Genomics, Proteomics, and Bioinformatics
-
-
Samuels, M.E.1
Dubé, M.P.2
-
5
-
-
0028786497
-
Toward fully automated genotyping: Genotyping microsatellite markers by deconvolution
-
Perlin, M.W.; Lancia, G.; Ng, S.K. Toward fully automated genotyping: genotyping microsatellite markers by deconvolution. Am. J. Hum. Genet. 1995, 57, 1199-1210.
-
(1995)
Am. J. Hum. Genet
, vol.57
, pp. 1199-1210
-
-
Perlin, M.W.1
Lancia, G.2
Ng, S.K.3
-
6
-
-
0001506104
-
Modulation of non-templated nucleotide addition by Taq DNA polymerase: Primer modifications that facilitate genotyping
-
Brownstein, M.J.; Carpten, J.D.; Smith, J.R. Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping. Biotechniques 1996, 20, 1004-6, 1008-10.
-
(1996)
Biotechniques
, vol.20
-
-
Brownstein, M.J.1
Carpten, J.D.2
Smith, J.R.3
-
7
-
-
0029763225
-
Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: Implications for PCR-based genotyping and cloning
-
Magnuson, V.L.; Ally, D.S.; Nylund, S.J.; Karanjawala, Z.E.; Rayman, J.B.; Knapp, J.I.; Lowe, A.L.; Ghosh, S.; Collins, F.S. Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloning. Biotechniques 1996, 21, 700-9.
-
(1996)
Biotechniques
, vol.21
, pp. 700-709
-
-
Magnuson, V.L.1
Ally, D.S.2
Nylund, S.J.3
Karanjawala, Z.E.4
Rayman, J.B.5
Knapp, J.I.6
Lowe, A.L.7
Ghosh, S.8
Collins, F.S.9
-
8
-
-
79959524146
-
A haplotype map of the human genome
-
Altshuler, D.; Brooks, L.D.; Chakravarti, A.; Collins, F.S.; Daly, M.J.; Donnelly, P. A haplotype map of the human genome. Nature 2005, 437, 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
Altshuler, D.1
Brooks, L.D.2
Chakravarti, A.3
Collins, F.S.4
Daly, M.J.5
Donnelly, P.6
-
9
-
-
0030814587
-
Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type C
-
Greer, W.L.; Riddell, D.C.; Byers, D.M.; Welch, J.P.; Girouard, G.S.; Sparrow, S.M.; Gillan, T.L.; Neumann, P.E. Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type C. Am. J. Hum. Genet. 1997, 61, 139-42.
-
(1997)
Am. J. Hum. Genet
, vol.61
, pp. 139-142
-
-
Greer, W.L.1
Riddell, D.C.2
Byers, D.M.3
Welch, J.P.4
Girouard, G.S.5
Sparrow, S.M.6
Gillan, T.L.7
Neumann, P.E.8
-
10
-
-
0033044278
-
Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease
-
Greer, W.L.; Riddell, D.C.; Murty, S.; Gillan, T.L.; Girouard, G.S.; Sparrow, S.M.; Tatlidil, C.; Dobson, M.J.; Neumann, P.E. Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease. Clin. Genet. 1999, 55, 248-55.
-
(1999)
Clin. Genet
, vol.55
, pp. 248-255
-
-
Greer, W.L.1
Riddell, D.C.2
Murty, S.3
Gillan, T.L.4
Girouard, G.S.5
Sparrow, S.M.6
Tatlidil, C.7
Dobson, M.J.8
Neumann, P.E.9
-
11
-
-
0030863352
-
-
Carstea, E.D.; Morris, J.A.; Coleman, K.G.; Loftus, S.K.; Zhang, D.; Cummings, C.; Gu, J.; Rosenfeld, M.A.; Pavan, W.J.; Krizman, D.B.; Nagle, J.; Polymeropoulos, M.H.; Sturley, S.L.; Ioannou, Y.A.; Higgins, M.E.; Comly, M.; Cooney, A.; Brown, A.; Kaneski, C.R.; Blanchette-Mackie, E.J.; Dwyer, N.K.; Neufeld, E.B.; Chang, T.Y.; Liscum, L.; Strauss III, J.F.; Ohno, K.; Zeigler, M.; Carmi, R.; Sokol, J.; Markie, D.; O'Neill, R.R.; van Diggelen, O. P.; Elleder, M.; Patterson, M.C.; Brady, R.O.; Vanier, M.T.; Pentchev, P.G.; Tagle, D. Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science 1997, 277, 228-31.
-
Carstea, E.D.; Morris, J.A.; Coleman, K.G.; Loftus, S.K.; Zhang, D.; Cummings, C.; Gu, J.; Rosenfeld, M.A.; Pavan, W.J.; Krizman, D.B.; Nagle, J.; Polymeropoulos, M.H.; Sturley, S.L.; Ioannou, Y.A.; Higgins, M.E.; Comly, M.; Cooney, A.; Brown, A.; Kaneski, C.R.; Blanchette-Mackie, E.J.; Dwyer, N.K.; Neufeld, E.B.; Chang, T.Y.; Liscum, L.; Strauss III, J.F.; Ohno, K.; Zeigler, M.; Carmi, R.; Sokol, J.; Markie, D.; O'Neill, R.R.; van Diggelen, O. P.; Elleder, M.; Patterson, M.C.; Brady, R.O.; Vanier, M.T.; Pentchev, P.G.; Tagle, D. Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science 1997, 277, 228-31.
-
-
-
-
12
-
-
0032231442
-
The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097 - >T transversion in NPC1
-
Greer, W.L.; Riddell, D.C.; Gillan, T.L.; Girouard, G.S.; Sparrow, S.M.; Byers, D.M.; Dobson, M.J.; Neumann, P.E. The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097 - >T transversion in NPC1. Am. J. Hum. Genet. 1998, 63, 52-4.
-
(1998)
Am. J. Hum. Genet
, vol.63
, pp. 52-54
-
-
Greer, W.L.1
Riddell, D.C.2
Gillan, T.L.3
Girouard, G.S.4
Sparrow, S.M.5
Byers, D.M.6
Dobson, M.J.7
Neumann, P.E.8
-
13
-
-
0030872838
-
PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
-
Nickerson, D.A.; Tobe, V.O.; Taylor, S.L. PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. Nucl. Acids Res. 1997, 25, 2745-51.
-
(1997)
Nucl. Acids Res
, vol.25
, pp. 2745-2751
-
-
Nickerson, D.A.1
Tobe, V.O.2
Taylor, S.L.3
-
14
-
-
0036795546
-
SNPCEQer: Detecting SNPs in sequences generated by the Beckman CEQ2000 DNA Analysis System
-
Flood, E.M.; Tang, F.; Horvath, M.M.; Pertsemlidis, A.; Garner, H.R. SNPCEQer: detecting SNPs in sequences generated by the Beckman CEQ2000 DNA Analysis System. Biotechniques 2002, 33, 814-20.
-
(2002)
Biotechniques
, vol.33
, pp. 814-820
-
-
Flood, E.M.1
Tang, F.2
Horvath, M.M.3
Pertsemlidis, A.4
Garner, H.R.5
-
15
-
-
15544369976
-
-
Weckx, S.; Del-Favero, J.; Rademakers, R.; Claes, L.; Cruts, M.; De Jonghe, P.; Van Broeckhoven, C.; De Rijk, P. novoSNP, a novel computational tool for sequence variation discovery. Genome Res. 2005, 15, 436-42.
-
Weckx, S.; Del-Favero, J.; Rademakers, R.; Claes, L.; Cruts, M.; De Jonghe, P.; Van Broeckhoven, C.; De Rijk, P. novoSNP, a novel computational tool for sequence variation discovery. Genome Res. 2005, 15, 436-42.
-
-
-
-
16
-
-
22144431577
-
-
Manaster, C.; Zheng, W.; Teuber, M.; Wachter, S.; Doring, F.; Schreiber, S.; Hampe, J. InSNP: a tool for automated detection and visualization of SNPs and InDels. Hum. Mutat. 2005, 26, 11-19.
-
Manaster, C.; Zheng, W.; Teuber, M.; Wachter, S.; Doring, F.; Schreiber, S.; Hampe, J. InSNP: a tool for automated detection and visualization of SNPs and InDels. Hum. Mutat. 2005, 26, 11-19.
-
-
-
-
17
-
-
25444448501
-
SeqDoC: Rapid SNP and mutation detection by direct comparison of DNA sequence chromatograms
-
Crowe, M.L. SeqDoC: rapid SNP and mutation detection by direct comparison of DNA sequence chromatograms. BMC Bioinform. 2005, 6, 133.
-
(2005)
BMC Bioinform
, vol.6
, pp. 133
-
-
Crowe, M.L.1
-
18
-
-
0033555906
-
Tandem repeats finder: A program to analyze DNA sequences
-
Benson, G. Tandem repeats finder: a program to analyze DNA sequences. Nucl. Acids Res. 1999, 27, 573-80.
-
(1999)
Nucl. Acids Res
, vol.27
, pp. 573-580
-
-
Benson, G.1
-
19
-
-
0037250168
-
The UCSC Genome Browser Database
-
Karolchik, D.; Baertsch, R.; Diekhans, M.; Furey, T.S.; Hinrichs, A.; Lu, Y.T.; Roskin, K.M.; Schwartz, M.; Sugnet, C.W.; Thomas, D.J.; Weber, R.J.; Haussler, D.; Kent, W.J. The UCSC Genome Browser Database. Nucl. Acids Res. 2003, 31, 51-4.
-
(2003)
Nucl. Acids Res
, vol.31
, pp. 51-54
-
-
Karolchik, D.1
Baertsch, R.2
Diekhans, M.3
Furey, T.S.4
Hinrichs, A.5
Lu, Y.T.6
Roskin, K.M.7
Schwartz, M.8
Sugnet, C.W.9
Thomas, D.J.10
Weber, R.J.11
Haussler, D.12
Kent, W.J.13
-
20
-
-
0036079158
-
The human genome browser at UCSC
-
Kent, W.J.; Sugnet, C.W.; Furey, T.S.; Roskin, K.M.; Pringle, T.H.; Zahler, A.M.; Haussler, D. The human genome browser at UCSC. Genome Res. 2002, 12, 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
Haussler, D.7
-
21
-
-
0034284437
-
Repbase Update: A database and an electronic journal of repetitive elements
-
Jurka, J. Repbase Update: a database and an electronic journal of repetitive elements. Trends Genet. 2000, 16, 418-20.
-
(2000)
Trends Genet
, vol.16
, pp. 418-420
-
-
Jurka, J.1
-
22
-
-
23844525077
-
Repbase Update, a database of eukaryotic repetitive elements
-
Jurka, J.; Kapitonov, V.V.; Pavlicek, A.; Klonowski, P.; Kohany, O.; Walichiewicz, J. Repbase Update, a database of eukaryotic repetitive elements. Cytogenet. Genome Res. 2005, 110, 462-7.
-
(2005)
Cytogenet. Genome Res
, vol.110
, pp. 462-467
-
-
Jurka, J.1
Kapitonov, V.V.2
Pavlicek, A.3
Klonowski, P.4
Kohany, O.5
Walichiewicz, J.6
-
23
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Rozen, S.; Skaletsky, H. Primer3 on the WWW for general users and for biologist programmers. Meth. Mol. Biol. 2000, 132, 365-86.
-
(2000)
Meth. Mol. Biol
, vol.132
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
24
-
-
0032231941
-
-
O'Connell, J.R.; Weeks, D.E. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am. J. Hum. Genet. 1998, 63, 259-66.
-
O'Connell, J.R.; Weeks, D.E. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am. J. Hum. Genet. 1998, 63, 259-66.
-
-
-
|