11p染色体标记的多点分析。

D E Goldgar, P R Fain
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Multipoint analysis of chromosome 11p markers.
The nature of the problems posed for the l l p segment of the fourth Genetic Analysis Workshop w e r e discussed in some detail i n the summary paper, as w e r e the characteristics of the two data sets available for analysis. W e assume that the reader is familiar w i t h the summary and therefore make no attenpt t o duplicate this information here. Our efforts in the analysis of the workshop data focvsed primarily on three different approaches t o the multipoint napping problem. Specifically, we wanted t o know i f gene order could be determined and a reasonable genetic map be constructed through the use of simple gametic counting procedures. Our second approach w a s t o analyze the data using a model incorporathy a prior distribution of chiasroata t o f i t relative genetic distances t o the obtained gametic frequency counts. This approach is similar t o the method which we described in GAW I11 (Fain and Goldgar, 1985). Use of these methak required that 4 locus phase could be determined either directly f m grandparental genotypes or indirectly from examination of very large sibshi~. Consequently, we concentrated our efforts on the large three generation families contained i n the WAFI data set, and our report w i l l be limited t o the analysis of t h i s data set.
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Genetic epidemiology: applications and comparisons of methods. Proceedings of Genetic Analysis Workshop IV. Snowbird, Utah, October 5-7, 1985. Genetic analysis workshop IV: Huntington disease linkage analysis, data description. A log-linear model for binary pedigree data. Linkage analysis of breast cancer among Utah and Dutch families using the sib-pair test. Linkage analysis of Dutch families at high risk for breast cancer.
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