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# Load a library necessary to run this code | |
library(stringi) | |
# Define the reverse complement function | |
rev.comp <- function(DNASeq) | |
return(stri_reverse(chartr("acgtACGT", "tgcaTGCA", DNASeq))) | |
# Run the code on the dataframe called DF | |
DF$Seq <- ifelse (DF$Strand == c("-"), rev.comp(DF$Seq), DF$Seq) | |
library(plyr) |
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# Load a library necessary to run this code | |
library(plyr) | |
# Run the code on the dataframes | |
CombinedDF <- join(MainDF, LookUpDF, by = "Column") | |
head(CombinedDF) |
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<h3> A standalone progress bar </h3> | |
<div class="fprogress" > | |
<div class="fprogress-bar" id="fA" style="width:90%"> <!-- Edit progress % here --> | |
<div class="fbox" id="fA" style="width: 232px"> <!-- Edit shaded area here --> | |
<span class="ftext">A Standalone Progress Bar</span> | |
</div> | |
</div> | |
</div> |
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xattr -d com.apple.quarantine file_name |
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Chromosomal Location | Summary | Reference |
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awk -F ',' '{print $<column_number>}' <file> | sort | uniq -c |