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		<title>imported&gt;Lab: 2022</title>
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		<updated>2022-05-08T01:46:40Z</updated>

		<summary type="html">&lt;p&gt;2022&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;; &amp;lt;div style=&amp;quot;font-size:180%&amp;quot;&amp;gt;BIOL 203 Bioinformatics Exercises for Lab 13&amp;lt;/div&amp;gt;&lt;br /&gt;
----&lt;br /&gt;
==Test phenotype-genotype association==&lt;br /&gt;
===Introduction: GWAS &amp;amp; Contingency Test===&lt;br /&gt;
Genome-Wide Association Study (GWAS) is a method for mapping phenotypes to genotypes. In a typical GWAS study, frequencies of alleles (e.g., C or T at position 785) are determined in a sample of affected individuals (the &amp;quot;cases&amp;quot; e.g. disease) as well as in a sample of unaffected individuals (the &amp;quot;controls&amp;quot;). For example, the following table shows results of a hypothetical case-control study at a locus segregating with two alleles (C and T):&lt;br /&gt;
&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
Table 1. Sample Genotype Frequencies&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! !! T/T !! T/C !! C/C !! Total&lt;br /&gt;
|-&lt;br /&gt;
| Case || 0 || 24 || 127 || ?&lt;br /&gt;
|-&lt;br /&gt;
| Control || 9 || 68 || 114 || ?&lt;br /&gt;
|-&lt;br /&gt;
| Total || ? || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Association between the genotype and the phenotype could be assessed with a [http://en.wikipedia.org/wiki/Contingency_table contingency table analysis]. In this case, &amp;amp;Chi;&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; = 26.4, p&amp;lt;0.0005, suggesting a significant association between genotypes and diseases. (By comparing the expected and observed counts, one could conclude that the C/C genotypes are over-represented in disease cases.)&lt;br /&gt;
&lt;br /&gt;
1. Perform an [http://www.physics.csbsju.edu/stats/contingency.html online contingency table analysis] using the hypothetical data in Table 1. Click on &amp;quot;other contingency tables&amp;quot; and do a 2-rows and 3-columns test with the data above. Your &amp;amp;Chi;&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; should be 26.4.&lt;br /&gt;
&lt;br /&gt;
2. Deriving from Table 1, fill the following table with allele counts. Then perform a 2-by-2 contingency table analysis using the link above.&lt;br /&gt;
For example, in the controls, the number of T alleles is: 18 + 68 = 86 , because homozygotes have two alleles and heterozygotes have one.&lt;br /&gt;
&lt;br /&gt;
Is there a statistically significant association between alleles and disease phenotype? Which allele (C or T) is over-represented in (i.e., statistically associated with) disease cases?&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
Table 2. Sample Allele Frequencies&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! !! T !! C !! Total&lt;br /&gt;
|-&lt;br /&gt;
| Case || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Control || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Total || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Test association with locus A===&lt;br /&gt;
Following the above two examples, perform both the genotype and allele association tests using the class data.&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
Table 3a. Genotype counts at Locus A&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  !! A1/A1 !! A1/A2 !! A2/A2 !! Row Sum&lt;br /&gt;
|-&lt;br /&gt;
| Taster || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Non-Taster || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Column Sum || ? || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Calculate allele counts &amp;amp; then test for association&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
Table 3b. Allele counts at Locus A&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  !! A1 !! A2 !! Row Sum&lt;br /&gt;
|-&lt;br /&gt;
| Taster || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Non-Taster || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Column Sum || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
Record your result in the lab report sheet for the contingency test for Locus A, including chi-square statistic, degree of freedom, and p values&lt;br /&gt;
===Test association with Locus B===&lt;br /&gt;
Table 4a. Genotype counts at Locus B for each phenotype&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  !! B1/B1 !! B1/B2 !! B1/B3 !! B2/B2 !! B2/B3 !! B3/B3!! Row Sum&lt;br /&gt;
|-&lt;br /&gt;
| Taster || ? || ? || ? || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Non-Taster || ? || ? || ? || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Column Sum || ? || ? || ? || ? || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
Calculate allele counts &amp;amp; then test for association&lt;br /&gt;
Table 4b. Allele counts at Locus B&lt;br /&gt;
&amp;lt;center&amp;gt;&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  !! B1 !! B2 !! B3 !! Row Sum&lt;br /&gt;
|-&lt;br /&gt;
| Taster || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Non-Taster || ? || ? || ? || ?&lt;br /&gt;
|-&lt;br /&gt;
| Column Sum || ? || ? || ? || ?&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/center&amp;gt;&lt;br /&gt;
Record your result in the lab report sheet for the contingency test for Locus A, including chi-square statistic, degree of freedom, and p values&lt;br /&gt;
==Web Exercise. Search for gene information using NCBI online databases==&lt;br /&gt;
# Point your browser to the [http://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE_TYPE=BlastSearch&amp;amp;BLAST_SPEC=OGP__9606__9558&amp;amp;LINK_LOC=blasthome NCBI Human Genome Resource] page&lt;br /&gt;
# Copy and paste sequence provided on Blackboard- this is the sequence of the gene associated with the taster phenotype&lt;br /&gt;
# Press &amp;quot;BLAST&amp;quot;. Copy &amp;amp; Paste the top hit in your final lab report.&lt;br /&gt;
# Briefly describe the function of the gene based on information found on the locus page&lt;br /&gt;
#to get to the gene locus page: click on the link for your hit--click on the &amp;quot;Feature&amp;quot; link (link describes the gene product)--the next page will be a GenBank page with protein and DNA sequence-- find the &amp;quot;Gene ID&amp;quot; which is a four-digit number-- click on it and you will be directed to the locus page&lt;br /&gt;
===Additional questions===&lt;br /&gt;
&lt;br /&gt;
Answer briefly (1-2 sentences):&lt;br /&gt;
# State what is the &amp;#039;&amp;#039;null hypothesis&amp;#039;&amp;#039; in a chi-square test &amp;amp; what is the &amp;#039;&amp;#039;alternative hypothesis&amp;#039;&amp;#039;&lt;br /&gt;
# Explain what probability is represented by the p-value. &lt;br /&gt;
# What can you conclude when p-value is &amp;#039;&amp;#039;&amp;#039;below&amp;#039;&amp;#039;&amp;#039; the threshold of significance (e.g., p = 0.05)?&lt;br /&gt;
# What would you conclude when p-value is &amp;#039;&amp;#039;&amp;#039;above&amp;#039;&amp;#039;&amp;#039; the critical value?&lt;br /&gt;
# Is there a statistically significant association between one of the alleles tested and the Taster phenotype? &lt;br /&gt;
# Which genotype is over-represented in the Non-Tasters?&lt;br /&gt;
# Which allele is over-represented in the Non-Tasters?&lt;/div&gt;</summary>
		<author><name>imported&gt;Lab</name></author>
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