[General] title = NS3570 logfile = cutandrun.log # If specified, this will be added to each submitted job as a comment label = JS # Specify non-standard adapters for trimmomatic, if necessary adapter = NexteraPE-PE.fa # List the different experimental conditions. Each condition may include multiple # biological replicates. For example, a wildtype and two different knockouts: conditions = Beas2B-Parental-aH3, Beas2B-Parental-aH3K4me3, Beas2B-Parental-aHA, Beas2B-H3WT-HA-aH3, Beas2B-H3WT-HA-aH3K4me3, Beas2B-H3WT-HA-aHA, Beas2B-H3E97K-HA-Clone19-aH3, Beas2B-H3E97K-HA-Clone19-aH3K4me3, Beas2B-H3E97K-HA-Clone19-aHA, Beas2B-H3E97K-HA-Clone22-aH3, Beas2B-H3E97K-HA-Clone22-aH3K4me3, Beas2B-H3E97K-HA-Clone22-aHA, Beas2B-H3E97K-HA-Clone23-aH3, Beas2B-H3E97K-HA-Clone23-aH3K4me3, Beas2B-H3E97K-HA-Clone23-aHA, Beas2B-H3E97K-HA-Clone19-IgG, Beas2B-H3E97K-HA-Clone22-IgG, Beas2B-H3E97K-HA-Clone23-IgG, Beas2B-H3WT-HA-IgG, Beas2B-Parental-IgG # Specify the differential analysis contrasts, separating each pair of samples with ^. contrasts = Beas2B-H3WT-HA-aH3^Beas2B-Parental-aH3, Beas2B-H3E97K-HA-Clone19-aH3^Beas2B-Parental-aH3, Beas2B-H3E97K-HA-Clone22-aH3^Beas2B-Parental-aH3, Beas2B-H3E97K-HA-Clone23-aH3^Beas2B-Parental-aH3, Beas2B-H3WT-HA-aH3K4me3^Beas2B-Parental-aH3K4me3, Beas2B-H3E97K-HA-Clone19-aH3K4me3^Beas2B-Parental-aH3K4me3, Beas2B-H3E97K-HA-Clone22-aH3K4me3^Beas2B-Parental-aH3K4me3, Beas2B-H3E97K-HA-Clone23-aH3K4me3^Beas2B-Parental-aH3K4me3, Beas2B-H3WT-HA-aHA^Beas2B-Parental-aHA, Beas2B-H3E97K-HA-Clone19-aHA^Beas2B-Parental-aHA, Beas2B-H3E97K-HA-Clone22-aHA^Beas2B-Parental-aHA, Beas2B-H3E97K-HA-Clone23-aHA^Beas2B-Parental-aHA, Beas2B-H3E97K-HA-Clone19-aHA^Beas2B-H3WT-HA-aHA, Beas2B-H3E97K-HA-Clone22-aHA^Beas2B-H3WT-HA-aHA, Beas2B-H3E97K-HA-Clone23-aHA^Beas2B-H3WT-HA-aHA, Beas2B-H3E97K-HA-Clone19-aH3^Beas2B-H3WT-HA-aH3, Beas2B-H3E97K-HA-Clone22-aH3^Beas2B-H3WT-HA-aH3, Beas2B-H3E97K-HA-Clone23-aH3^Beas2B-H3WT-HA-aH3, Beas2B-H3E97K-HA-Clone19-aH3K4me3^Beas2B-H3WT-HA-aH3K4me3, Beas2B-H3E97K-HA-Clone22-aH3K4me3^Beas2B-H3WT-HA-aH3K4me3, Beas2B-H3E97K-HA-Clone23-aH3K4me3^Beas2B-H3WT-HA-aH3K4me3 # False discovery rate fdr = 0.05 steps = samples, -fastqcount.1, -trim, -fastqcount.2, -bowtie, -bamcount.1, -spikein, -markdupfast, -bamcount.2, -merge, -bamcov, seacr, -frip, seacrdiff, -multiqc, hub #stopAt = fastp [Spikeins] spikeidx = /data/reference/icbr/BACTERIA/Escherichia_coli_K_12_MG1655/NCBI/2001-10-15/Sequence/Bowtie2Index/genome scalebam = False [SEACR] topfrac = 0.05 norm = False mode = stringent enhancers = /data/reference/icbr/DATABASES/Enhancers/enhanceratlas.org/3T3-L1_EP.bed [Hub] # Directives for automatic genome browser hub creation. genome = hg38 sizes = /data/reference/icbr/GRCh38/hg38.chrom.sizes hubname = hub shortLabel = NS3570 longLabel = dirname = NS3570 url = https://bw:bw@lichtlab.cancer.ufl.edu/reports/H2B/ [Include] # All genome files are listed in a separate conf file genome = /data/reference/icbr/GRCh38/GENOMEFILES # If fastqs are listed in a separate file, use this fastqs = fastqs.conf