| Whitehead_Library | R Documentation |
A data frame with a named row for each sgRNA of the Whitehead sgRNA library [1] including annotations such as targeted genes, and genomic coordinates.
data(Whitehead_Library)
A a row named data frame with 181131 observations of the following variables (among others)
CODEalphanumerical identifier of the sgRNAs;
GENEStargeted gene;
STARTposstarting genomic coordinate of the targeted genomic region (numeric);
STRANDtargeted DNA strand ('sense' or 'antisense')
EXONEexone of the targeted genomic region (exone number);
CHRMchromosome of where the targeted region resides (string)
ENDposending genomic coordinate of the targeted genomic region (numeric).
seqnucelotidic sequence of the sgRNAs without the PAM. (string).
Discontinued by Addgene
[1] Wang T, Birsoy K, Hughes NW, et al. Identification and characterization of essential genes in the human genome. Science. 2015;350(6264):1096-1101. doi:10.1126/science.aac7041
## Not run:
## Loading sgRNA Whitehead library annotation file
data(Whitehead_Library)
## Visualising first entries
head(Whitehead_Library)
## Deriving the path of an example count file
## from screening the HT-29 cell line with the Whitehead library
## [2]
fn<-paste(system.file('extdata', package = 'CRISPRcleanR'),
'/HT-29-Whitehead_counts.tsv',sep='')
expName<-'HT29-Whitehead'
## Loading, median-normalizing and computing fold-changes
normANDfcs<-
ccr.NormfoldChanges(filename = fn,
display = TRUE,
min_reads = 30,
EXPname = expName,
libraryAnnotation = Whitehead_Library)
## Genome-sorting the fold changes
gwSortedFCs<-
ccr.logFCs2chromPos(foldchanges = normANDfcs$logFCs,
libraryAnnotation = Whitehead_Library)
## Identifying and correcting biased sgRNAs' fold changes
correctedFCs_and_segments<-
ccr.GWclean(gwSortedFCs = gwSortedFCs,
display=TRUE,
label=expName)
## End(Not run)
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