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snake_conf.yaml
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#
# This is the Snakemake configuration file that specifies paths and
# and options for the Combined Haplotype Pipeline
#
{
# py2 is a bit of a hack so that python2 scripts can be called
# by snakemake (which is written in python3). The value should
# do whatever is needed to setup a python2 environment and
# call the python2 interpreter. Depending on your system configuration,
# this might involve setting the PATH environment variable or
# just calling python2
"py2" : "PATH=$HOME/anaconda2/bin:$PATH; python ",
# Rscript should set environment as appropriate and call Rscript interpreter
"Rscript" : "PATH=$HOME/anaconda2/bin:$PATH; Rscript ",
# WASP directory
"wasp_dir" : "/iblm/netapp/home/gmcvicker/proj/WASP",
# directory to write all output data files to
"base_dir" : "/iblm/netapp/home/gmcvicker/proj/WASP/CHT/output",
# minimum number of allele-specific reads (combined across individuals)
# required to perform combined test on a region
"min_as_count" : "10",
# location of chromInfo file containing chromosome names and lengths
# (can be downloaded from UCSC genome browser)
"chrom_info" : "/iblm/netapp/home/gmcvicker/proj/WASP/examples/example_data/chromInfo.hg19.txt",
# directory containing impute or VCF SNP files
"snp_dir" : "/iblm/netapp/home/gmcvicker/proj/WASP/examples/example_data/genotypes",
# file containing sample identifiers for impute or VCF SNP file
"snp_samples" : "/iblm/netapp/home/gmcvicker/proj/WASP/examples/example_data/genotypes/YRI_samples.txt",
# directory containing bowtie2 index
# one file per chromosome
"fasta_dir" : "/iblm/netapp/data1/external/GRC37/chroms",
# text file containing sample identifiers for the subset of
# samples that are used in study (one per line)
"samples_file" : "/iblm/netapp/home/gmcvicker/proj/WASP/examples/example_data/H3K27ac/samples.txt",
# directory containing BAM files
"bam_dir" : "/iblm/netapp/home/gmcvicker/proj/WASP/examples/example_data/H3K27ac",
# postfix of BAM files
"bam_postfix" : ".keep.rmdup.bam"
}