[General] title = NSD2_CS_RCHACV_070218_Mohammad logfile = chipseq.log project = https://basespace.illumina.com/run/96022930/UTX_CS_ARP_HA_KARPAS_061218_DAPHNE # If specified, this will be added to each submitted job as a comment label = JDL-NSD2-CS # 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 = 2C-EZH2, 2C-H2AK119ub, 2C-H3K27ac, 2C-H3K27me3, 2C-H3K36me2, 2C-NSD2, 9B-EZH2, 9B-H2AK119ub, 9B-H3K27ac, 9B-H3K27me3, 9B-H3K36me2, 9B-NSD2 # Specify the differential analysis contrasts, separating each pair of samples with ^. contrasts = 2C-EZH2^9B-EZH2, 2C-H2AK119ub^9B-H2AK119ub, 2C-H3K27ac^9B-H3K27ac, 2C-H3K27me3^9B-H3K27me3, 2C-H3K36me2^9B-H3K36me2, 2C-NSD2^9B-NSD2 # False discovery rate fdr = 0.05 steps = samples, -fastqcount.1, -trim, -fastqcount.2, -bowtie, -bamcount.1, -markdup, -bamcount.2, -merge, -bamcov, -bamtowig, -macs, -tags, -peaks, -diffpeaks, -motifs, -insertsize, -multiqc, hub [bamtowig] #scale = 1000 [Hub] dirname = hub genome = hg38 #hubname = sizes = hg38.chrom.sizes shortLabel = NSD2_CS_RCHACV_070218 longLabel = NSD2_CS_RCHACV_070218 ChIP-Seq email = lichtlab.common@gmail.com url = http://licht:licht@lichtlab.cancer.ufl.edu/reports/NSD2/ [Include] fastq = fastqs.conf genome = /ufrc/data/reference/icbr/GRCh38/GENOMEFILES [2C-EZH2] samples = RCHACV-2C-EZH2 [2C-H2AK119ub] samples = RCHACV-2C-H2AK119ub [2C-H3K27ac] samples = RCHACV-2C-H3K27ac [2C-H3K27me3] samples = RCHACV-2C-H3K27me3 [2C-H3K36me2] samples = RCHACV-2C-H3K36me2 [2C-NSD2] samples = RCHACV-2C-NSD2 [9B-EZH2] samples = RCHACV-9B-EZH2 [9B-H2AK119ub] samples = RCHACV-9B-H2AK119ub [9B-H3K27ac] samples = RCHACV-9B-H3K27ac [9B-H3K27me3] samples = RCHACV-9B-H3K27me3 [9B-H3K36me2] samples = RCHACV-9B-H3K36me2 [9B-NSD2] samples = RCHACV-9B-NSD2