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GATK4 first round without MuTect1 and indel realignment #607
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c9b2cd9
QR for posters
428c893
Dockerand singularity images for vcfanno
6f438ad
removing superfluous routines, adding comments
e00872b
logging improvements
f6c60bf
nfcore based image file containing vcfanno and qc modules also
a3f102d
on a way to unify to nf-core and GATK4
576c171
It works without indelrealignment until CreateRecalibrationTable
0aea380
new target directories for Prerocessing, works to the end of ApplyBQSR
72a1b50
HaplotypeCaller works with GATK4
c6137bf
path and version fixed for both manta and strelka
bba73f1
Mutect2 GATK4 initial dumb version
70a3584
Added genome index file
a836057
Changed Dockerfile to follow https://github.com/nf-core/methylseq/pul…
733e2c4
removed -Xmx4g because it was ignored anyway and made a syntax/workfl…
449f939
alphabetical order and added freebayes and new htslib version
3fb6dc6
freebayes and igvtools in the core container
0c71f0a
set -euo pipefail needed also for germline
da3be40
die mutect1
4db0d5d
commenting out AFs as it will be for a new sprint
efd11c6
vcfanno is merged to the core
e81e100
removed igvtools (as went to core)
0876a89
Merge remote-tracking branch 'upstream/master'
7cf77b6
Not using the log util, as it is not working
e2cacd7
fixed indent
735463b
gatk-launch rename
a64dd3c
MarkDuplicates got all the memory
c14fa8e
Merge branch 'master' of github.com:szilvajuhos/Sarek
5ab4491
Latest versions
537faa8
MarkDuplicates MAX_RECORDS_IN_RAM decreased to 50000
24b1ffb
Picard removed from buildReferences.nf
a5b3f7c
adding all the cpus and mem to MarkDuplicates
6ebed7a
update submodule Sarek-data a.k.a. #609
58bab13
s/gatk-launch/gatk/
12826fd
removing realign parts
b21dc68
removing realign parts
db137ce
small review changes
cb7e228
Merge branch 'master' of github.com:szilvajuhos/Sarek
97d3fc5
adding singularty environments for tests
98cf879
VEP fancy parametrisation
393da8b
memory adjustments for samtools and MarkDuplicates
9d20c68
s/sarek-core/sarek/ also deleting build.sh
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| Original file line number | Diff line number | Diff line change |
|---|---|---|
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@@ -14,7 +14,7 @@ env { | |
| params { | ||
| genome_base = params.genome == 'GRCh37' ? '/sw/data/uppnex/ToolBox/ReferenceAssemblies/hg38make/bundle/2.8/b37' : params.genome == 'GRCh38' ? '/sw/data/uppnex/ToolBox/hg38bundle' : 'References/smallGRCh37' | ||
| singleCPUMem = 8.GB | ||
| totalMemory = 104.GB // change to 240 on irma | ||
| totalMemory = 92.GB // change to 240 on irma | ||
|
Member
There was a problem hiding this comment. Choose a reason for hiding this commentThe reason will be displayed to describe this comment to others. Learn more. Why did you change to 92?
Collaborator
Author
There was a problem hiding this comment. Choose a reason for hiding this commentThe reason will be displayed to describe this comment to others. Learn more. by mistake |
||
| } | ||
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||
| executor { | ||
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@@ -70,7 +70,7 @@ process { | |
| memory = {params.totalMemory} | ||
| } | ||
| $MarkDuplicates { | ||
| memory = {params.singleCPUMem * 2 * task.attempt} | ||
| // for deep sequencing we do need all the memory | ||
| } | ||
| $MergeBams { | ||
| cpus = 16 | ||
|
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@@ -117,10 +117,6 @@ process { | |
| } | ||
| $RunMultiQC { | ||
| } | ||
| $RunMutect1 { | ||
| cpus = 1 | ||
| memory = {params.singleCPUMem * task.attempt} | ||
| } | ||
| $RunMutect2 { | ||
| cpus = 1 | ||
| memory = {params.singleCPUMem * task.attempt} | ||
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In fact, we annote all available vcfs by default, so it's not really a question of germline/somatic, but really more a question of which tools was run