AA BB CODD -log10(p) Now imagine that you've done a GWAS with those 10 SNPs, plus 7000 SNPs which are not associated with the phenotype. Here are 4 Manhattan plots log10(P) 10 8 4 10 8 6 A (d)01601- 10 8 1 2 3 4 5 6 7 8 9 10 X 2 3 4 5 6 7 8 9 10 X Chromosome Chromosome ...C 10 1 2 4 5 6 7 8 9 10 X Chromosome logo(p) 2 8 6 1 2 3 4 5 6 7 8 9 10 X Chromosome Which plot is most representative of what you found? Remember that the chromosomes are along the x axis, the log 10 pvalue is the y axis, and each point is an individual SNP. ..B D
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- Which of the following chromosome rearrangement genotypes and/or processes involving the described chromosome rearrangement can lead to unbalanced gametes? (Select all correct answers.) .00000 translocation heterozygote recombination outside of the inversion loop formed in a pericentric inversion heterozygote translocation homozygote pericentric inversion homozygote recombination within an inversion loop formed in a paracentric inversion heterozygote187:12 What is not true for Sequence tagged site (STS) markers: O cannot be mapped by fluorescence in situ hybridization (FISH) O subset of STS markers are known as expressed sequence tag (EST) markers O can readily be screened by a PCR assay O short DNA sequences that occur at a unique location in the genome
- Calculate the number of Alu elements present in the haploid human genome based on the number of Alu elements present in the clones analysed by the entire class. You will need to know the total length of DNA analysed and the number of Alu elements present. For the entire class, 57 Alu elements are present in 174,204 bp.Please atleast answer this questionA pair of paralogous repeats, A and B, have 96% sequence similarity and therefore can promote non-allelic homologous recombination (NAHR). They exist in four possible arrangements in a genome, illustrated below as arrangements 1 – 4. What is the result of NAHR between repeats A and B in arrangement 1? A.Translocation between chromosomes 1 and 2 resulting in monocentric chromosomes B.Deletion or duplication of the region between A and B C.Translocation between chromosomes 1 and 2 resulting in acentric and dicentric chromosomes D.Inversion of the region between A and B