View source: R/analysis-functions.R
CIS_grubbs | R Documentation |
Statistical approach for the validation of common insertion sites significance based on the comparison of the integration frequency at the CIS gene with respect to other genes contained in the surrounding genomic regions. For more details please refer to this paper: https://ashpublications.org/blood/article/117/20/5332/21206/Lentiviral-vector-common-integration-sites-in
CIS_grubbs(
x,
genomic_annotation_file = "hg19",
grubbs_flanking_gene_bp = 1e+05,
threshold_alpha = 0.05,
by = NULL,
return_missing_as_df = TRUE,
results_as_list = TRUE
)
x |
An integration matrix, must include the |
genomic_annotation_file |
Database file for gene annotation, see details. |
grubbs_flanking_gene_bp |
Number of base pairs flanking a gene |
threshold_alpha |
Significance threshold |
by |
Either |
return_missing_as_df |
Returns those genes present in the input df but not in the refgenes as a data frame? |
results_as_list |
If |
A data frame containing
genes annotation for the specific genome.
From version 1.5.4
the argument genomic_annotation_file
accepts only
data frames or package provided defaults.
The user is responsible for importing the appropriate tabular files if
customization is needed.
The annotations for the human genome (hg19) and
murine genome (mm9) are already
included in this package: to use one of them just
set the argument genomic_annotation_file
to either "hg19"
or
"mm9"
.
If for any reason the user is performing an analysis on another genome,
this file needs to be changed respecting the USCS Genome Browser
format, meaning the input file headers should include:
name2, chrom, strand, min_txStart, max_txEnd, minmax_TxLen, average_TxLen, name, min_cdsStart, max_cdsEnd, minmax_CdsLen, average_CdsLen
A data frame
The function will explicitly check for the presence of these tags:
chromosome
locus
is_strand
gene_symbol
gene_strand
Other Analysis functions:
HSC_population_size_estimate()
,
compute_abundance()
,
cumulative_is()
,
gene_frequency_fisher()
,
is_sharing()
,
iss_source()
,
sample_statistics()
,
top_integrations()
,
top_targeted_genes()
data("integration_matrices", package = "ISAnalytics")
cis <- CIS_grubbs(integration_matrices)
cis
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