-
1
-
-
0035131982
-
The impact of genotyping error on family-based analysis of quantitative traits
-
Abecasis GR, Cherny SS, Cardon LR: The impact of genotyping error on family-based analysis of quantitative traits. Eur J Hum Genet 2001;9:130-134.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 130-134
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cardon, L.R.3
-
2
-
-
0025942732
-
Influence of aberrant observations on high-resolution linkage analysis outcomes
-
Buetow KH: Influence of aberrant observations on high-resolution linkage analysis outcomes. Am J Hum Genet 1991;49:985-994.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 985-994
-
-
Buetow, K.H.1
-
3
-
-
0033941023
-
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data
-
Douglas JA, Boehnke M, Lange K: A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet 2000;66:1287-1297.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1287-1297
-
-
Douglas, J.A.1
Boehnke, M.2
Lange, K.3
-
4
-
-
0030964440
-
The effects of genotyping errors and interference on estimation of genetic distance
-
Goldstein DR, Zhao H, Speed TP: The effects of genotyping errors and interference on estimation of genetic distance. Hum Hered 1997;47:86-100.
-
(1997)
Hum Hered
, vol.47
, pp. 86-100
-
-
Goldstein, D.R.1
Zhao, H.2
Speed, T.P.3
-
5
-
-
0036157589
-
Detection and integration of genotyping errors in statistical genetics
-
Sobel E, Papp JC, Lange K: Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet 2002;70:496-508.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 496-508
-
-
Sobel, E.1
Papp, J.C.2
Lange, K.3
-
6
-
-
0029655834
-
Error detection for genetic data, using likelihood methods
-
Ehm MG, Kimmel M, Cottingham RWJ: Error detection for genetic data, using likelihood methods. Am J Hum Genet 1996;58:225-234.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 225-234
-
-
Ehm, M.G.1
Kimmel, M.2
Cottingham, R.W.J.3
-
7
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR: Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
8
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE: PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998;63:259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
9
-
-
0036154960
-
Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data
-
Douglas JA, Skol AD, Boehnke M: Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. Am J Hum Genet 2002;70:487-495.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 487-495
-
-
Douglas, J.A.1
Skol, A.D.2
Boehnke, M.3
-
10
-
-
34248669832
-
An examination of the genotyping error detection function of SIMWALK2
-
Badzioch MD, DeFrance HB, Jarvik GP: An examination of the genotyping error detection function of SIMWALK2. BMC Genet 2003;4(suppl 1):S40.
-
(2003)
BMC Genet
, vol.4
, Issue.1 SUPPL.
-
-
Badzioch, M.D.1
DeFrance, H.B.2
Jarvik, G.P.3
-
11
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K: Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 1996;58:1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
12
-
-
0033643184
-
An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: Implications for study design
-
Gordon D, Leal SM, Heath SC, Ott J: An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: Implications for study design. Pac Symp Biocomput 2000:663-674.
-
(2000)
Pac Symp Biocomput
, pp. 663-674
-
-
Gordon, D.1
Leal, S.M.2
Heath, S.C.3
Ott, J.4
-
13
-
-
0027213849
-
Chromosome-based method for rapid computer simulation in human genetic linkage analysis
-
Terwilliger JD, Speer M, Ott J: Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genet Epidemiol 1993;10:217-224.
-
(1993)
Genet Epidemiol
, vol.10
, pp. 217-224
-
-
Terwilliger, J.D.1
Speer, M.2
Ott, J.3
-
14
-
-
0003325270
-
Mega2, a data-handling program for facilitating genetic linkage and association analyses
-
Mukhopadhyay N, Almasy L, Schroeder M, Mulvihill WP, Weeks DE: Mega2, a data-handling program for facilitating genetic linkage and association analyses. Am J Hum Genet 1999;65:A436.
-
(1999)
Am J Hum Genet
, vol.65
-
-
Mukhopadhyay, N.1
Almasy, L.2
Schroeder, M.3
Mulvihill, W.P.4
Weeks, D.E.5
-
15
-
-
0345659239
-
Summary report: Missing data and pedigree and genotyping errors
-
Badzioch MD, Thomas DC, Jarvik GP: Summary report: Missing data and pedigree and genotyping errors. Genet Epidemiol 2003;25(suppl 1):S36-42.
-
(2003)
Genet Epidemiol
, vol.25
, Issue.1 SUPPL.
-
-
Badzioch, M.D.1
Thomas, D.C.2
Jarvik, G.P.3
-
16
-
-
0034917944
-
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data
-
Gordon D, Heath SC, Liu X, Ott J: A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet 2001;69:371-380.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 371-380
-
-
Gordon, D.1
Heath, S.C.2
Liu, X.3
Ott, J.4
-
17
-
-
0033942718
-
Linkage analysis in the presence of errors II: Marker-locus genotyping errors modeled with hypercomplex recombination fractions
-
Goring HH, Terwilliger JD: Linkage analysis in the presence of errors II: Marker-locus genotyping errors modeled with hypercomplex recombination fractions. Am J Hum Genet 2000;66:1107-1118.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1107-1118
-
-
Goring, H.H.1
Terwilliger, J.D.2
-
18
-
-
0042320432
-
Multipoint and single point non-parametric linkage analysis with imperfect data
-
Sullivan PF, Neale BM, Neale MC, van den Oord E, Kendler KS: Multipoint and single point non-parametric linkage analysis with imperfect data. Am J Med Genet Part B (Neuropsych Genet) 2003;121B:89-94.
-
(2003)
Am J Med Genet Part B (Neuropsych Genet)
, vol.121 B
, pp. 89-94
-
-
Sullivan, P.F.1
Neale, B.M.2
Neale, M.C.3
Van Den Oord, E.4
Kendler, K.S.5
-
19
-
-
1842859051
-
Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms
-
Gordon D, Finch SJ, Nothnagel M, Ott J: Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms. Hum Hered 2002;54:22-33.
-
(2002)
Hum Hered
, vol.54
, pp. 22-33
-
-
Gordon, D.1
Finch, S.J.2
Nothnagel, M.3
Ott, J.4
-
20
-
-
0942276432
-
What SNP genotyping errors are most costly for genetic association studies?
-
Kang SJ, Gordon D, Finch SJ: What SNP genotyping errors are most costly for genetic association studies? Genet Epidemiol 2004;26:132-141.
-
(2004)
Genet Epidemiol
, vol.26
, pp. 132-141
-
-
Kang, S.J.1
Gordon, D.2
Finch, S.J.3
-
21
-
-
0042629677
-
Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies
-
Gordon D, Levenstien MA, Finch SJ, Ott J: Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies. Pac Symp Biocomput 2003:490-501.
-
(2003)
Pac Symp Biocomput
, pp. 490-501
-
-
Gordon, D.1
Levenstien, M.A.2
Finch, S.J.3
Ott, J.4
|