A 2006 genetic study of a large American family (Ikeda et al., 2006) identified genetic linkage between DNA markers on chromosome 11 and the gene producing the autosomal dominant neuromuscular disorder spinocerebellar ataxia type 5 (SCA5). The following lod score data are taken from the 2006 study:                                     Theta (θ) Value               0.01    0.05     0.10     0.20     0.30     0.40SCA5    11.02   12.26   11.94   10.04    7.26     3.77 and DNA marker A SCA5    0.35.    0.94.     1.07     0.99     0.75    0.43 and DNA marker B Does either group of lod scores indicate statistically significant odds in favor of genetic linkage? Explain your answer.

Neurofibromatosis 1 (NF1) is an autosomal dominant disorder inherited on human chromosome 17. Part of the analysis mapping the NF1 gene to chromosome 17 came from genetic linkage studies testing segregation of NF1 and DNA genetic markers on various chromosomes. A DNA marker with two alleles, designated 1 and 2, is linked to NF1. The pedigree below shows segregation of NF1 (darkened symbols) and gives genotypes for the DNA marker for each family member.

Determine the alleles for the NF1 gene and the DNA marker gene on each chromosome carried by the four family members in generation I and generation II. Use N for the dominant NF1 allele and n for the recessive allele and assume I-1 is heterozygous for the disease allele (Nn). <>

A 2006 genetic study of a large American family (Ikeda et al., 2006) identified genetic linkage between DNA markers on chromosome 11 and the gene producing the autosomal dominant neuromuscular disorder spinocerebellar ataxia type 5 (SCA5). The following lod score data are taken from the 2006 study:                                     Theta (θ) Value               0.01    0.05     0.10     0.20     0.30     0.40SCA5    11.02   12.26   11.94   10.04    7.26     3.77 and DNA marker A SCA5    0.35.    0.94.     1.07     0.99     0.75    0.43 and DNA marker B Based on the available information, is DNA marker A linked to the gene producing SCA5? Explain your answer.

A 2006 genetic study of a large American family (Ikeda et al., 2006) identified genetic linkage between DNA markers on chromosome 11 and the gene producing the autosomal dominant neuromuscular disorder spinocerebellar ataxia type 5 (SCA5). The following lod score data are taken from the 2006 study:                                     Theta (θ) Value               0.01    0.05     0.10     0.20     0.30     0.40SCA5    11.02   12.26   11.94   10.04    7.26     3.77 and DNA marker A SCA5    0.35.    0.94.     1.07     0.99     0.75    0.43 and DNA marker B What is the maximum value for each set of lod scores?

A 2006 genetic study of a large American family (Ikeda et al., 2006) identified genetic linkage between DNA markers on chromosome 11 and the gene producing the autosomal dominant neuromuscular disorder spinocerebellar ataxia type 5 (SCA5). The following lod score data are taken from the 2006 study:

                                    Theta (θ) Value
               0.01    0.05     0.10     0.20     0.30     0.40
SCA5    11.02   12.26   11.94   10.04    7.26     3.77
and
DNA
marker A

SCA5    0.35.    0.94.     1.07     0.99     0.75    0.43
and
DNA
marker B

Based on available information, is DNA marker B linked to the gene for SCA5? Explain your answer.

A genetic study of an early onset form of heart disease identifies 10 families containing members with the condition. No clear dominant or recessive pattern of inheritance is evident, but an analysis of SNP markers for five families detects a strong association with a marker on chromosome 12, and genetic linkage analysis for the marker produces a lod score of 2.2.

What next step do you recommend for this genetic analysis?

A genetic study of an early onset form of heart disease identifies 10 families containing members with the condition. No clear dominant or recessive pattern of inheritance is evident, but an analysis of SNP markers for five families detects a strong association with a marker on chromosome 12, and genetic linkage analysis for the marker produces a lod score of 2.2.

What do the association and lod score results suggest about this genetic marker?