ND STONY BROOK UNIVERSITY LOOSELEAF GENETICS: FROM GENES TO GENOMES
ND STONY BROOK UNIVERSITY LOOSELEAF GENETICS: FROM GENES TO GENOMES
6th Edition
ISBN: 9781260406092
Author: HARTWELL, Leland, HOOD, Leroy, Goldberg, Michael
Publisher: Mcgraw-hill Education/stony Brook University
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Chapter 22, Problem 26P

ALS (amyotrophic lateral sclerosis) is a rare, fatal neurodegenerative disease that is genetically complex. During the last several years, using GWAS analyses and other methods, 11 different genes have been identified that are thought to be connected with ALS. The most recently discovered of these genes, TBK1, was identified through analysis of the whole exome sequences of several thousand Cases and Controls. Recall from Chapter 11 that the exome is the approximately 1% of the human genome that corresponds to exons. Each person’s exome sequence was evaluated on a gene-by-gene basis as to whether or not a SNP variant likely to alter gene function was present. The TBK1 gene was not identified in previous GWAS analyses that genotyped similar numbers of individuals for common SNPs. Cite possible explanations for the different outcomes of these two experiments.

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this is what i have said about this image so far, what else can be said aswell including the raw count column. "   Interpreting the results of an RNA-Seq analysis is pivotal in understanding the underlying genetic mechanisms of diseases such as breast cancer. In this analysis, Figure 1 provides comprehensive data on differentially expressed genes associated with breast cancer. By delving into the provided information, we can gain valuable insights into the molecular landscape of this disease. First focus is on the gene with the highest fold change, EYA4, situated on chromosome 6. With a staggering fold change of 3604.4176, EYA4 exhibits an unprecedented level of overexpression in cancerous cells compared to normal cells. This profound alteration suggests a pivotal role for EYA4 in breast cancer pathogenesis. The log2 fold change of 11.81555 further emphasizes the magnitude of this difference in gene expression. Statistical significance is evident, with an exceptionally low p-value of…
Cap, EA1, and Sap are all genes/proteins of interest in this study. For each gene, what gene product is encoded and where is the gene (the literal DNA sequence) located physically in the cell?    I need help fimiding this in the artticle and answer as short as possible  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC106848/
People who carry a theoretical genetic disorder (called B-disease) can be identified from a 2kb DNA sequence. People who carry this genetic disorder have a single nucleotide polymorphism that results in a change of GTATTC to GGATTC, a site that only occurs once at nucleotide number 750 in this DNA sequence. Answer the following questions based on the information provided. a) How can you develop a simple molecular test to identify the genetic disorder?

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ND STONY BROOK UNIVERSITY LOOSELEAF GENETICS: FROM GENES TO GENOMES

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