opening_act2 | R Documentation |
Runs the lab's standard analysis of ChIP-seq experiment data and produces
several .pdf files of analysis plots to be kept in a new folder at
.../LabShare/HTGenomics/Opening_act/
.
opening_act2( signal_data, genome, genotype, chip_target, sample_id, output_path = "/Volumes/LabShare/HTGenomics/Opening_act/", user_input = TRUE, run_chr_size_bias = TRUE, run_centromeres = TRUE, run_rDNA = TRUE, run_telomeres = TRUE, run_dsb_hotspots = TRUE, run_axis = TRUE, run_meta_orf = TRUE )
signal_data |
Input signal track data as a |
genome |
Character object specifying the genome version; accepts one of the following options:
No default. |
genotype |
Character object indicating the relevant strain mutations.
Just use |
chip_target |
Character object indicating the ChIP target protein. No default. |
sample_id |
Character object indicating the sample ID, including the ID
used in the analysis pipeline (with a date) and the read mapping conditions
(see examples below). If |
output_path |
Character object with a valid path to directory to save
output files at. Defaults to
|
user_input |
Logical indicating whether to ask user to check the format
of the |
run_chr_size_bias |
Logical indicating whether to run the chromosome
size bias analysis. All included analysis can be turned off in this way.
Defaults to |
run_centromeres |
Logical indicating whether to run the signal at
centromere analysis. Defaults to |
run_rDNA |
Logical indicating whether to run the signal flanking rDNA
analysis. Defaults to |
run_telomeres |
Logical indicating whether to run the signal at
sub-telomeric region analysis. Defaults to |
run_dsb_hotspots |
Logical indicating whether to run the signal at DSB
hotspot analysis. Defaults to |
run_axis |
Logical indicating whether to run the signal at axis binding
site analysis. Defaults to |
run_meta_orf |
Logical indicating whether to run the meta ORF analysis.
Defaults to |
A new folder at the specified location (default is
.../LabShare/HTGenomics/Opening_act/
) containing output plots (as .pdf
files) of the included of the following analyses:
Chromosome size bias
Signal at centromeres
Signal flanking rDNA
Signal at sub-telomeric regions
Signal at DSB hotspots
Signal at axis binding sites
Signal at meta ORF
## Not run: opening_act2(signal_data=WT, genome="sacCer3", genotype="WT", chip_target="Red1", sample_id="AH119C-040114-sacCer3-2mis") opening_act2(set1_wiggle, genome="sacCer3", "set1", "Red1", "AH8584b-16032016-sacCer3-2mis") opening_act2(rec8, genome="SK1Yue", "rec8", "Red1", "AH8115b-24042015-SK1Yue-PM", user_input=FALSE, run_meta_orf=FALSE) opening_act2(signal_data=WT, genome="sacCer3", genotype="WT", chip_target="Red1", sample_id="AH119C-040114-sacCer3-2mis", run_meta_orf=FALSE) opening_act2(signal_data=WT, genome="sacCer3", genotype="dot1", chip_target="Red1", sample_id="AH8104-010116-sacCer3-2mis", output_path='~/Desktop', run_chr_size_bias=FALSE, run_centromeres=FALSE, run_rDNA=FALSE, run_telomeres=FALSE, run_dsb_hotspots=TRUE, run_axis=TRUE, run_meta_orf=FALSE) ## End(Not run)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.