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settings.conf.backup
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----------------------------------------------------
Settings file for haploid enrichment screen scripts
----------------------------------------------------
Description:
All parameters are tab separated. Don't edit the name of the parameter.
# These settings are always required (ie. for additional_gene_mapping.sh and additional_gene_mapping.sh)
#########################################################################################################
Parameter value description
---------------------------------------
gene_ref: /scratch/ENRICHMENT/ref/HG19_ref_unique.BED # File containing list with genes and their genomic position
ref_id: unique # A human readable and somewhat comprehensive tag for this gene reference file (for example concatenated or unique)
core_num: 20 # Desired number of CPU cores to be used
memory_limit: 20G # Amount of RAM available for analysis
# These settings are only applicable to the Full Analysis Pipeline (ie. full_enrichment_analysis.sh)
######################################################################################################
Parameter value description
---------------------------------------
location_bowtie : /usr/local/bin/bowtie # enter full path
ref_genome: /scratch/reference_files/BOWTIE_HG19/hg19 # path to directory incl. invariable part of file name
control_dataset: /media/analyzed_data/enrichment_screens/control_data_HG19/seq.fastq.uniqReads_mapped_UNIQ
trim_reads: yes # 'yes' or 'no'
keep_reads_from: 0 # from which base should the reads be kept? (0 for beginning of read)
desired_read_length: 50 # new read length
mismatch_num: 1 # Number of mismatches allowed, cannot be more the 1
final_dir: /media/analyzed_data/enrichment_screens/ # To which directory should the files be written to if the analysis is done (please put / behind it!)