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13 changes: 13 additions & 0 deletions Intro_Biocomp_ND_317_Tutorial7.Rproj
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Version: 1.0

RestoreWorkspace: Default
SaveWorkspace: Default
AlwaysSaveHistory: Default

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UseSpacesForTab: Yes
NumSpacesForTab: 2
Encoding: UTF-8

RnwWeave: Sweave
LaTeX: pdfLaTeX
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55 changes: 55 additions & 0 deletions tut7RScript.R
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#Tutorial Exercise 7
#Shane Davitt (No partner as I was the odd one out in our tutorial section)
#
#Question 1
#
#{Plotting by Sequence Lengths}
#
#Putting Lecture11.fasta into an R object
fastaData=read.table("Lecture11.fasta", sep="\t")

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you're going to want to use scan() here.

#
#Removing seq labels
conFasta = fastaData[seq(2, nrow(fastaData),2),]
#
#Converting data to a dataframe
data.frame(conFasta)
#
#Counting number of charecters in each sequence
countFasta=apply(conFasta,1,nchar)
#
#Plotting the result as a histogram
seqLenPlot=hist(countFasta, xlab="Sequence Length")
#
#{Plotting by GC Content (proportion of sequence which is GC)}
#
#Counting Gs in each sequence
gCount=str_count(conFasta[,1], pattern="G")
#
#Counting Cs in each sequence
cCount=str_count(conFasta[,1], pattern="C")
#
#Total GC count in each seq
GCCount=gCount+cCount
#
#Getting proportion of seq which is GC
GCfreq=GCCount/countFasta
#
#Plotting GC proportion as histogram
GCfreqPlot=hist(GCfreq, xlab="GC Proportion")
#
#I love it when manipulating matrices is as simple as a plus
#and a minus sign ! :)
#
#{Ouestion 2}
#
#Reading my data
crimeData=read.csv("crimeData.csv")
#
#Turning into R object
crimeTable=data.frame(crimeData)
#
#Plotting Data
plot(crimeTable[,2],crimeTable[,1], type="p", xlab="Median Household Income", ylab="Property Crime Rate", main="Examining Affluence and Crime", sub="(TX Counties, 2015)")
#
#Plotting trendline
abline(lm(crimeTable[,1]~crimeTable[,2],crimeTable))