atac_dnase_pipelines
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MACS2 Set pValue to -1 and terrifies IDR
Hi It seems MACS2 Set pValue for some peaks to -1 and IDR cannot accept that and crashed have to convert all -1 to 0 and it worked
AB2955-L1_R1.trim.PE2SE.nodup.pr1.tn5.pf.500K.pval0.01.narrowPeak.gz chr16 67192014 67192579 Peak_102120 34 . 3.17360 3.48800 1.21916 319 chr16 89923548 89923621 Peak_102121 34 . 3.17360 3.48800 1.21916 -1 chr16 2223989 2224074 Peak_102119 34 . 3.17360 3.48800 1.21916 8 chr14 102140051 102140159 Peak_102118 34 . 3.17360 3.48800 1.21916 66 chr14 100110943 100111138 Peak_102117 34 . 3.17360 3.48800 1.21916 17 chr13 82549279 82549524 Peak_102116 34 . 3.17360 3.48800 1.21916 101
usr/local/envs/bds_atac_py3/bin/idr --samples /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/pseudo_reps/rep1/pr1/AB2955-L1_R1.trim.PE2SE.nodup.pr1.tn5.pf.500K.pval0.01.narrowPeak.gz /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/pseudo_reps/rep1/pr2/AB2955-L1_R1.trim.PE2SE.nodup.pr2.tn5.pf.500K.pval0.01.narrowPeak.gz --peak-list /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/rep1/AB2955-L1_R1.trim.PE2SE.nodup.tn5.pf.500K.pval0.01.narrowPeak.gz --input-file-type narrowPeak --output-file /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/idr/pseudo_reps/rep1/VA2.7+CCR6+CCR2+_rep1-pr.unthresholded-peaks.txt --rank p.value --soft-idr-threshold 0.05 --plot --use-best-multisummit-IDR --log-output-file /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/idr/pseudo_reps/rep1/VA2.7+CCR6+CCR2+_rep1-pr.IDR0.05.log.txt
Traceback (most recent call last):
File "/usr/local/envs/bds_atac_py3/bin/idr", line 4, in
ARGUMENTS LIST: name = /gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/peak/macs2/pooled_pseudo_reps/ppr2/AB2955-L1_R1.trim.PE2SE.nodup.pr2.tn5_AB2959-L1_R1.trim.PE2SE.nodup.pr2.tn5.pf format = BED ChIP-seq file = ['/gs6/users/shamsaddinisha/jfarber-20160119-E1/VA2.7+CCR6+CCR2+/hg38/align/pooled_pseudo_reps/ppr2/AB2955-L1_R1.trim.PE2SE.nodup.pr2.tn5_AB2959-L1_R1.trim.PE2SE.nodup.pr2.tn5.tagAlign.gz'] control file = None effective genome size = 2.70e+09 band width = 300 model fold = [5, 50] pvalue cutoff = 1.00e-02
qvalue will not be calculated and reported as -1 in the final output.
Larger dataset will be scaled towards smaller dataset. Range for calculating regional lambda is: 10000 bps Broad region calling is off Searching for subpeak summits is on MACS will save fragment pileup signal per million reads