TY - JOUR
T1 - Segregation analysis of 159 soft tissue sarcoma kindreds
T2 - Comparison of fixed and sequential sampling schemes
AU - Bondy, Melissa L.
AU - Lustbader, Edward D.
AU - Strom, Sara S.
AU - Strong, Louise C.
AU - Chakravarti, Aravinda
PY - 1992
Y1 - 1992
N2 - In this study we compared parameter estimates and model hypotheses in pedigree data collected by fixed sampling with estimates and hypotheses derived by sequential sampling. Employing a fixed sampling scheme, we previously analyzed data on relatives of 159 childhood sarcoma patients. We have now extracted from that data set individuals who would have been included in a sequentially sampled study. We applied segregation analysis to the truncated data, to determine the mode of inheritance and major locus parameter estimates. With data from both sampling schemes we made a family‐by‐family comparison to determine each family's contribution to a major gene model. The two sampling schemes yielded similar results: we detected segregation of a dominant major gene and obtained similar major locus parameter estimates. However, the sequential sampling scheme derived these conclusions from data on 982 relatives rather than the 2,451 ascertained in the fixed sampling scheme. The sequential sampling scheme failed to identify only one of the kindreds likely to be segregating the gene. For this data set, the sequential sampling scheme would have provided an efficient mechanism to discriminate genetic hypotheses and would have permitted focus of resources on the specific kindreds likely to segregate a major gene. © 1992 Wiley‐Liss, Inc.
AB - In this study we compared parameter estimates and model hypotheses in pedigree data collected by fixed sampling with estimates and hypotheses derived by sequential sampling. Employing a fixed sampling scheme, we previously analyzed data on relatives of 159 childhood sarcoma patients. We have now extracted from that data set individuals who would have been included in a sequentially sampled study. We applied segregation analysis to the truncated data, to determine the mode of inheritance and major locus parameter estimates. With data from both sampling schemes we made a family‐by‐family comparison to determine each family's contribution to a major gene model. The two sampling schemes yielded similar results: we detected segregation of a dominant major gene and obtained similar major locus parameter estimates. However, the sequential sampling scheme derived these conclusions from data on 982 relatives rather than the 2,451 ascertained in the fixed sampling scheme. The sequential sampling scheme failed to identify only one of the kindreds likely to be segregating the gene. For this data set, the sequential sampling scheme would have provided an efficient mechanism to discriminate genetic hypotheses and would have permitted focus of resources on the specific kindreds likely to segregate a major gene. © 1992 Wiley‐Liss, Inc.
KW - epidemiological methods
KW - family studies
KW - genetic epidemiology
KW - sampling schemes
KW - soft tissue sarcoma
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U2 - 10.1002/gepi.1370090502
DO - 10.1002/gepi.1370090502
M3 - Article
C2 - 1427019
AN - SCOPUS:0026459752
SN - 0741-0395
VL - 9
SP - 291
EP - 304
JO - Genetic Epidemiology
JF - Genetic Epidemiology
IS - 5
ER -