| HT.29correctedFCs | R Documentation |
This list contains corrected sgRNAs log fold-changes and segment annotations for an example cell line (HT-29), obtained using the ccr.GWclean function, as detailed in its reference manual entry ccr.GWclean.
data("HT.29correctedFCs")
A list containing two data frames and a vector of strings. The first data frame (corrected_logFCs) contains a named row per each sgRNA and the following columns/header:
CHR: the chromosome of the gene targeted by the sgRNA under consideration;
startp: the genomic coordinate of the starting position of the region targeted by the sgRNA under consideration;
endp: the genomic coordinate of the ending position of the region targeted by the sgRNA under consideration;
genes: the HGNC symbol of the gene targeted by the sgRNA under consideration;
avgFC: the log fold change of the sgRNA averaged across replicates;
correction: the type of correction: 1 = increased log fold change, -1 = decreased log fold change. 0 indicates no correction;
correctedFC: the corrected log fold change of the sgRNA
.
The second data frame (segments) contains the identified region of estimated equal log fold changes (one region per row) and the following
columns/headers:
CHR: the chromosome of the gene targeted by the sgRNA under consideration;
startp: the genomic coordinate of the starting position of the region targeted by the sgRNA under consideration;
endp: the genomic coordinate of the ending position of the region targeted by the sgRNA under consideration;
genes: the HGNC symbol of the gene targeted by the sgRNA under consideration;
avgFC: the log fold change of the sgRNA averaged across replicates;
correction: the type of correction: 1 = increased log fold change, -1 = decreased log fold change. 0 indicates no correction;
correctedFC: the corrected log fold change of the sgRNA
.
The second data frame (segments) contains the identified region of estimated equal log fold changes (one region per row) and the following
columns/headers:
CHR: the chromosome of the region under consideration;
startp: the genomic coordinate of the starting position of the region under consideration;
endp: the genomic coordinate of the ending position of the region under consideration;
n.sgRNAs: the number of sgRNAs targeting sequences in the region under consideration;
avg.logFC: the average log fold change of the sgRNAs in the region;
guideIdx: the indexes range of the sgRNAs targeting the region under consideration as they appear in the gwSortedF Cs provided in input.
The string of vectors (SORTED_sgRNAs) contains the sgRNAs' identifiers in the same order as they are reported in the gwSortedFCs data frame inputted to the ccr.GWclean function.
data(HT.29correctedFCs)
head(HT.29correctedFCs$corrected_logFCs)
head(HT.29correctedFCs$segments)
head(HT.29correctedFCs$SORTED_sgRNAs)
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