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Hello! This is an automated update of the following workflow: workflows/epigenetics/atacseq. I created this PR because I think one or more of the component tools are out of date, i.e. there is a newer version available on the ToolShed.
By comparing with the latest versions available on the ToolShed, it seems the following tools are outdated:
toolshed.g2.bx.psu.edu/repos/devteam/picard/picard_MarkDuplicates/2.18.2.4 should be updated to toolshed.g2.bx.psu.edu/repos/devteam/picard/picard_MarkDuplicatesWithMateCigar/2.18.2.3
The workflow release number has been updated from 0.9 to 0.10.
gxydevbot
changed the title
Updating workflows/epigenetics/atacseq from 0.9 to 0.10
Updating workflows/epigenetics/atacseq from 0.9 to 0.10
Mar 14, 2024
Output with path /tmp/tmpcvar0dh4/mapping stats__effcccaf-2c9f-46e2-a991-eeb349576927 different than expected
Expected text '32872 (11.70%) aligned concordantly 0 times' in output ('280859 reads; of these:
280859 (100.00%) were paired; of these:
63325 (22.55%) aligned concordantly 0 times
92695 (33.00%) aligned concordantly exactly 1 time
124839 (44.45%) aligned concordantly >1 times
----
63325 pairs aligned concordantly 0 times; of these:
22423 (35.41%) aligned discordantly 1 time
----
40902 pairs aligned 0 times concordantly or discordantly; of these:
81804 mates make up the pairs; of these:
20792 (25.42%) aligned 0 times
16976 (20.75%) aligned exactly 1 time
44036 (53.83%) aligned >1 times
96.30% overall alignment rate
')
Output with path /tmp/tmpg46z1ng4/BAM filtered rmDup__ad709c8c-8efa-4177-bc89-cfffafb4cf93 different than expected
Expected file size of 14134105+-1000000 found 12297725
Output with path /tmp/tmp9dufh6fe/MACS2 narrowPeak__accce04d-d400-4016-84e2-c2091bd2ccc6 different than expected
Expected 225+-0 lines in the output found 164
Output with path /tmp/tmpd4h9_lyq/MACS2 report__2f76034b-7764-4d13-ba67-ef2a267af997 different than expected
Expected text '# tag size is determined as 47 bps' in output ('# This file is generated by MACS version 2.2.9.1
# Command line: callpeak -t /tmp/tmp54uix5l3/files/b/b/f/dataset_bbfcf8c1-2427-4950-90ae-16c4f29b3340.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmp54uix5l3/files/b/b/f/dataset_bbfcf8c1-2427-4950-90ae-16c4f29b3340.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is on
# tag size is determined as 49 bps
# total tags in treatment: 203732
# Sequencing ends will be shifted towards 5' by 100 bp(s)
# d = 200
')
Output with path /tmp/tmp20kim_yv/Coverage from MACS2 (bigwig)__533c9d55-600d-4c82-9473-a711c3a4d8d9 different than expected
Expected file size of 2594908+-200000 found 2279659
Output with path /tmp/tmpi5zpahcy/Summits +-500bp (merged)__b540adf4-aeb1-4e77-a060-d9a18548f85b different than expected
Expected 213+-0 lines in the output found 157
Output with path /tmp/tmpzitbiwcq/Nb of reads in summits +-500bp__f1393e0d-49d7-4095-a90b-0dc140a44a21 different than expected
Expected line '8802' in output ('6057
')
Output with path /tmp/tmpvv0znvg9/bigwig normalized per million reads in peaks__1200b8df-9ea2-46ba-a1d8-52619a1bad9c different than expected
Expected file size of 1133795+-100000 found 1031113
INFO @ Thu, 14 Mar 2024 12:09:00:
# Command line: callpeak -t /tmp/tmp54uix5l3/files/b/b/f/dataset_bbfcf8c1-2427-4950-90ae-16c4f29b3340.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmp54uix5l3/files/b/b/f/dataset_bbfcf8c1-2427-4950-90ae-16c4f29b3340.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is onINFO @ Thu, 14 Mar 2024 12:09:00: #1 read tag files... INFO @ Thu, 14 Mar 2024 12:09:00: #1 read treatment tags... INFO @ Thu, 14 Mar 2024 12:09:00: #1 tag size is determined as 49 bps INFO @ Thu, 14 Mar 2024 12:09:00: #1 tag size = 49.0 INFO @ Thu, 14 Mar 2024 12:09:00: #1 total tags in treatment: 203732 INFO @ Thu, 14 Mar 2024 12:09:00: #1 finished! INFO @ Thu, 14 Mar 2024 12:09:00: #2 Build Peak Model... INFO @ Thu, 14 Mar 2024 12:09:00: #2 Skipped... INFO @ Thu, 14 Mar 2024 12:09:00: #2 Use 200 as fragment length INFO @ Thu, 14 Mar 2024 12:09:00: #2 Sequencing ends will be shifted towards 5' by 100 bp(s) INFO @ Thu, 14 Mar 2024 12:09:00: #3 Call peaks... INFO @ Thu, 14 Mar 2024 12:09:00: #3 Going to call summits inside each peak ... INFO @ Thu, 14 Mar 2024 12:09:00: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 14 Mar 2024 12:09:01: #3 In the peak calling step, the following will be performed simultaneously: INFO @ Thu, 14 Mar 2024 12:09:01: #3 Write bedGraph files for treatment pileup (after scaling if necessary)... SRR891268_chr22_enriched_treat_pileup.bdg INFO @ Thu, 14 Mar 2024 12:09:01: #3 Write bedGraph files for control lambda (after scaling if necessary)... SRR891268_chr22_enriched_control_lambda.bdg INFO @ Thu, 14 Mar 2024 12:09:01: #3 Pileup will be based on sequencing depth in treatment. INFO @ Thu, 14 Mar 2024 12:09:01: #3 Call peaks for each chromosome... INFO @ Thu, 14 Mar 2024 12:09:01: #4 Write output xls file... SRR891268_chr22_enriched_peaks.xls INFO @ Thu, 14 Mar 2024 12:09:01: #4 Write peak in narrowPeak format file... SRR891268_chr22_enriched_peaks.narrowPeak INFO @ Thu, 14 Mar 2024 12:09:01: #4 Write summits bed file... SRR891268_chr22_enriched_summits.bed INFO @ Thu, 14 Mar 2024 12:09:01: Done!
/usr/local/bin/picard: line 5: warning: setlocale: LC_ALL: cannot change locale (en_US.UTF-8): No such file or directoryPicked up _JAVA_OPTIONS: -Xmx2048m -Xms256m -Djava.io.tmpdir=/tmp/tmp54uix5l3/tmpMar 14, 2024 12:08:15 PM com.intel.gkl.NativeLibraryLoader loadINFO: Loading libgkl_compression.so from jar:file:/usr/local/share/picard-3.1.1-0/picard.jar!/com/intel/gkl/native/libgkl_compression.so
Output with path /tmp/tmpdrj16buc/mapping stats__dab83fb4-27e6-4568-9e0c-cc3b431886bb different than expected
Expected text '32872 (11.70%) aligned concordantly 0 times' in output ('280964 reads; of these:
280964 (100.00%) were paired; of these:
30410 (10.82%) aligned concordantly 0 times
109333 (38.91%) aligned concordantly exactly 1 time
141221 (50.26%) aligned concordantly >1 times
----
30410 pairs aligned concordantly 0 times; of these:
13319 (43.80%) aligned discordantly 1 time
----
17091 pairs aligned 0 times concordantly or discordantly; of these:
34182 mates make up the pairs; of these:
6127 (17.92%) aligned 0 times
6515 (19.06%) aligned exactly 1 time
21540 (63.02%) aligned >1 times
98.91% overall alignment rate
')
Output with path /tmp/tmpgxj711qm/MACS2 narrowPeak__fefb57d0-52cc-4964-955c-452f8428a548 different than expected
Expected 225+-0 lines in the output found 223
Output with path /tmp/tmpqi6nrc7h/MACS2 report__f7dd6ed0-87c4-492b-b5a7-0c03a77a0ae6 different than expected
Expected text '# total tags in treatment: 234432' in output ('# This file is generated by MACS version 2.2.9.1
# Command line: callpeak -t /tmp/tmpsrn7tro1/files/9/a/8/dataset_9a8288ab-efc6-44e8-ae05-7c2ddc949ae7.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmpsrn7tro1/files/9/a/8/dataset_9a8288ab-efc6-44e8-ae05-7c2ddc949ae7.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is on
# tag size is determined as 47 bps
# total tags in treatment: 232804
# Sequencing ends will be shifted towards 5' by 100 bp(s)
# d = 200
')
Output with path /tmp/tmpu0syxtlv/Summits +-500bp (merged)__fd8c2250-72cf-470b-abb4-35b69df76f2d different than expected
Expected 213+-0 lines in the output found 211
Output with path /tmp/tmpfo0beo2x/Nb of reads in summits +-500bp__8231ceee-110b-4a43-9f17-a0d0a842ce6d different than expected
Expected line '8802' in output ('8698
')
INFO @ Thu, 14 Mar 2024 12:30:54:
# Command line: callpeak -t /tmp/tmpsrn7tro1/files/9/a/8/dataset_9a8288ab-efc6-44e8-ae05-7c2ddc949ae7.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmpsrn7tro1/files/9/a/8/dataset_9a8288ab-efc6-44e8-ae05-7c2ddc949ae7.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is onINFO @ Thu, 14 Mar 2024 12:30:54: #1 read tag files... INFO @ Thu, 14 Mar 2024 12:30:54: #1 read treatment tags... INFO @ Thu, 14 Mar 2024 12:30:55: #1 tag size is determined as 47 bps INFO @ Thu, 14 Mar 2024 12:30:55: #1 tag size = 47.0 INFO @ Thu, 14 Mar 2024 12:30:55: #1 total tags in treatment: 232804 INFO @ Thu, 14 Mar 2024 12:30:55: #1 finished! INFO @ Thu, 14 Mar 2024 12:30:55: #2 Build Peak Model... INFO @ Thu, 14 Mar 2024 12:30:55: #2 Skipped... INFO @ Thu, 14 Mar 2024 12:30:55: #2 Use 200 as fragment length INFO @ Thu, 14 Mar 2024 12:30:55: #2 Sequencing ends will be shifted towards 5' by 100 bp(s) INFO @ Thu, 14 Mar 2024 12:30:55: #3 Call peaks... INFO @ Thu, 14 Mar 2024 12:30:55: #3 Going to call summits inside each peak ... INFO @ Thu, 14 Mar 2024 12:30:55: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 14 Mar 2024 12:30:55: #3 In the peak calling step, the following will be performed simultaneously: INFO @ Thu, 14 Mar 2024 12:30:55: #3 Write bedGraph files for treatment pileup (after scaling if necessary)... SRR891268_chr22_enriched_treat_pileup.bdg INFO @ Thu, 14 Mar 2024 12:30:55: #3 Write bedGraph files for control lambda (after scaling if necessary)... SRR891268_chr22_enriched_control_lambda.bdg INFO @ Thu, 14 Mar 2024 12:30:55: #3 Pileup will be based on sequencing depth in treatment. INFO @ Thu, 14 Mar 2024 12:30:55: #3 Call peaks for each chromosome... INFO @ Thu, 14 Mar 2024 12:30:56: #4 Write output xls file... SRR891268_chr22_enriched_peaks.xls INFO @ Thu, 14 Mar 2024 12:30:56: #4 Write peak in narrowPeak format file... SRR891268_chr22_enriched_peaks.narrowPeak INFO @ Thu, 14 Mar 2024 12:30:56: #4 Write summits bed file... SRR891268_chr22_enriched_summits.bed INFO @ Thu, 14 Mar 2024 12:30:56: Done!
/usr/local/bin/picard: line 5: warning: setlocale: LC_ALL: cannot change locale (en_US.UTF-8): No such file or directoryPicked up _JAVA_OPTIONS: -Xmx2048m -Xms256m -Djava.io.tmpdir=/tmp/tmpsrn7tro1/tmpMar 14, 2024 12:30:09 PM com.intel.gkl.NativeLibraryLoader loadINFO: Loading libgkl_compression.so from jar:file:/usr/local/share/picard-3.1.1-0/picard.jar!/com/intel/gkl/native/libgkl_compression.so
INFO @ Thu, 14 Mar 2024 13:30:51:
# Command line: callpeak -t /tmp/tmp89xn9jz6/files/6/7/f/dataset_67fdf7ff-a7e9-40be-8906-430d5a80d12e.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmp89xn9jz6/files/6/7/f/dataset_67fdf7ff-a7e9-40be-8906-430d5a80d12e.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is onINFO @ Thu, 14 Mar 2024 13:30:51: #1 read tag files... INFO @ Thu, 14 Mar 2024 13:30:51: #1 read treatment tags... INFO @ Thu, 14 Mar 2024 13:30:51: #1 tag size is determined as 47 bps INFO @ Thu, 14 Mar 2024 13:30:51: #1 tag size = 47.0 INFO @ Thu, 14 Mar 2024 13:30:51: #1 total tags in treatment: 232804 INFO @ Thu, 14 Mar 2024 13:30:51: #1 finished! INFO @ Thu, 14 Mar 2024 13:30:51: #2 Build Peak Model... INFO @ Thu, 14 Mar 2024 13:30:51: #2 Skipped... INFO @ Thu, 14 Mar 2024 13:30:51: #2 Use 200 as fragment length INFO @ Thu, 14 Mar 2024 13:30:51: #2 Sequencing ends will be shifted towards 5' by 100 bp(s) INFO @ Thu, 14 Mar 2024 13:30:51: #3 Call peaks... INFO @ Thu, 14 Mar 2024 13:30:51: #3 Going to call summits inside each peak ... INFO @ Thu, 14 Mar 2024 13:30:51: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 14 Mar 2024 13:30:52: #3 In the peak calling step, the following will be performed simultaneously: INFO @ Thu, 14 Mar 2024 13:30:52: #3 Write bedGraph files for treatment pileup (after scaling if necessary)... SRR891268_chr22_enriched_treat_pileup.bdg INFO @ Thu, 14 Mar 2024 13:30:52: #3 Write bedGraph files for control lambda (after scaling if necessary)... SRR891268_chr22_enriched_control_lambda.bdg INFO @ Thu, 14 Mar 2024 13:30:52: #3 Pileup will be based on sequencing depth in treatment. INFO @ Thu, 14 Mar 2024 13:30:52: #3 Call peaks for each chromosome... INFO @ Thu, 14 Mar 2024 13:30:53: #4 Write output xls file... SRR891268_chr22_enriched_peaks.xls INFO @ Thu, 14 Mar 2024 13:30:53: #4 Write peak in narrowPeak format file... SRR891268_chr22_enriched_peaks.narrowPeak INFO @ Thu, 14 Mar 2024 13:30:53: #4 Write summits bed file... SRR891268_chr22_enriched_summits.bed INFO @ Thu, 14 Mar 2024 13:30:53: Done!
/usr/local/bin/picard: line 5: warning: setlocale: LC_ALL: cannot change locale (en_US.UTF-8): No such file or directoryPicked up _JAVA_OPTIONS: -Xmx2048m -Xms256m -Djava.io.tmpdir=/tmp/tmp89xn9jz6/tmpMar 14, 2024 1:30:03 PM com.intel.gkl.NativeLibraryLoader loadINFO: Loading libgkl_compression.so from jar:file:/usr/local/share/picard-3.1.1-0/picard.jar!/com/intel/gkl/native/libgkl_compression.so
INFO @ Thu, 14 Mar 2024 14:13:16:
# Command line: callpeak -t /tmp/tmp1c8vk83u/files/9/c/7/dataset_9c74e81d-288d-4942-8e77-02508f98f62f.dat --name SRR891268_chr22_enriched --format BED --gsize 2700000000 --call-summits --keep-dup all --d-min 20 --buffer-size 100000 --bdg --qvalue 0.05 --nomodel --extsize 200 --shift -100
# ARGUMENTS LIST:
# name = SRR891268_chr22_enriched
# format = BED
# ChIP-seq file = ['/tmp/tmp1c8vk83u/files/9/c/7/dataset_9c74e81d-288d-4942-8e77-02508f98f62f.dat']
# control file = None
# effective genome size = 2.70e+09
# band width = 300
# model fold = [5, 50]
# qvalue cutoff = 5.00e-02
# The maximum gap between significant sites is assigned as the read length/tag size.
# The minimum length of peaks is assigned as the predicted fragment length "d".
# Larger dataset will be scaled towards smaller dataset.
# Range for calculating regional lambda is: 10000 bps
# Broad region calling is off
# Paired-End mode is off
# Searching for subpeak summits is onINFO @ Thu, 14 Mar 2024 14:13:16: #1 read tag files... INFO @ Thu, 14 Mar 2024 14:13:16: #1 read treatment tags... INFO @ Thu, 14 Mar 2024 14:13:16: #1 tag size is determined as 47 bps INFO @ Thu, 14 Mar 2024 14:13:16: #1 tag size = 47.0 INFO @ Thu, 14 Mar 2024 14:13:16: #1 total tags in treatment: 232804 INFO @ Thu, 14 Mar 2024 14:13:16: #1 finished! INFO @ Thu, 14 Mar 2024 14:13:16: #2 Build Peak Model... INFO @ Thu, 14 Mar 2024 14:13:16: #2 Skipped... INFO @ Thu, 14 Mar 2024 14:13:16: #2 Use 200 as fragment length INFO @ Thu, 14 Mar 2024 14:13:16: #2 Sequencing ends will be shifted towards 5' by 100 bp(s) INFO @ Thu, 14 Mar 2024 14:13:16: #3 Call peaks... INFO @ Thu, 14 Mar 2024 14:13:16: #3 Going to call summits inside each peak ... INFO @ Thu, 14 Mar 2024 14:13:16: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 14 Mar 2024 14:13:16: #3 In the peak calling step, the following will be performed simultaneously: INFO @ Thu, 14 Mar 2024 14:13:16: #3 Write bedGraph files for treatment pileup (after scaling if necessary)... SRR891268_chr22_enriched_treat_pileup.bdg INFO @ Thu, 14 Mar 2024 14:13:16: #3 Write bedGraph files for control lambda (after scaling if necessary)... SRR891268_chr22_enriched_control_lambda.bdg INFO @ Thu, 14 Mar 2024 14:13:16: #3 Pileup will be based on sequencing depth in treatment. INFO @ Thu, 14 Mar 2024 14:13:16: #3 Call peaks for each chromosome... INFO @ Thu, 14 Mar 2024 14:13:17: #4 Write output xls file... SRR891268_chr22_enriched_peaks.xls INFO @ Thu, 14 Mar 2024 14:13:17: #4 Write peak in narrowPeak format file... SRR891268_chr22_enriched_peaks.narrowPeak INFO @ Thu, 14 Mar 2024 14:13:17: #4 Write summits bed file... SRR891268_chr22_enriched_summits.bed INFO @ Thu, 14 Mar 2024 14:13:17: Done!
/usr/local/bin/picard: line 5: warning: setlocale: LC_ALL: cannot change locale (en_US.UTF-8): No such file or directoryPicked up _JAVA_OPTIONS: -Xmx2048m -Xms256m -Djava.io.tmpdir=/tmp/tmp1c8vk83u/tmpMar 14, 2024 2:12:30 PM com.intel.gkl.NativeLibraryLoader loadINFO: Loading libgkl_compression.so from jar:file:/usr/local/share/picard-3.1.1-0/picard.jar!/com/intel/gkl/native/libgkl_compression.so
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Hello! This is an automated update of the following workflow: workflows/epigenetics/atacseq. I created this PR because I think one or more of the component tools are out of date, i.e. there is a newer version available on the ToolShed.
By comparing with the latest versions available on the ToolShed, it seems the following tools are outdated:
toolshed.g2.bx.psu.edu/repos/devteam/picard/picard_MarkDuplicates/2.18.2.4should be updated totoolshed.g2.bx.psu.edu/repos/devteam/picard/picard_MarkDuplicatesWithMateCigar/2.18.2.3The workflow release number has been updated from 0.9 to 0.10.