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ChIP-seq
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IGR-lab
ChIP-seq
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b57ad27db664a78e156e3f2912fcb2dba6fde709
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Created with Raphaël 2.2.0
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Jun
workflowr set up
master
master
set up
Start workflowr project.
annotated
annotations updated
change filename
added annotations
clean up
change folders
rearranging scripts
new SSH key
duplicate file
updated
first commit
added chainCleaner
updated
added links to scripts for lastz ad repeak masker
first commit
generate commands to run array scripts for lastz and repeatMasker
changed directory name to ouput peak calls for 10M reads per sample
changed directory to call peaks on 10M reads
edited snakemake command
first commit - subsample BAM files to the desired read number
first commit - script parses a multiFASTA and output a separate fasta file for each sequence header
first commit of conda environment with packages for whole genome alignment
added repeat masking steps
altered to run on 10M subsampled BAM files
first commit. script to subsample BAM files in a directory
edit input/output folders to run peak calling pipeline on subsampled BAM files
added -snakefile flag to command to call a specific snakefile
created separate config files for each histone mark
created separate snakefiles for histone marks as I couldn't get the wildcards to work so had to hardcode one of the rules
added info on converting to 2bit format
rule for calculating frip in replicate peaks
added merged input
added input control
adding merging of input control BAM files
added frip for comparing replicate peaks to pooled peaks
commented out to fix bug later
change directory
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