Releases: molgenis/NGS_DNA
4.0.2 (GATK4 pipeline)
- updated all tool versions for running on gearshift
3.5.5 (Uakari)
-
replaced hard filter FS for SOR
- for indels: "FS > 200.0" is now "SOR > 10.0"
- for snps: "FS > 60.0" is now "SOR > 3.0"
-
added fastQ information to the header of the vcf
-
added gendercheck information to resultsfolder (was not in resultsfolder before)
3.5.4 (Tiger)
updates:
-
requesting resources for a protocol is now handled via a parameters file (bigger datasets sometimes require more resources). all #MOLGENIS headers are removed from the protocols. This can now be used with the new Molgenis-Compute (see below)
-
reads with a mapping quality below 20 will not be used in calculating coverage
-
new Molgenis-Compute-19.01.1-Java-11.0.2 version (before: Molgenis-Compute-17.08.1-Java-1.8.0_74)
bugfixes:
- (diagnostics) fixing ONCO_v5 issue. The pipeline will execute genderCheck automatically when there is chrX available. ONCO_v5 has only a very small percentage of targets on chrX which is not reliable enough. fix: when ONCO, no GenderCheck
- rejected samples (due to no or 0.0% reads for a barcode) were not removed from the samplesheet.
- Gavin bugfix: when choosing option BOTH the merged INFO fields will be pasted directly to the other INFO fields without a separator, this is now fixed (with perl replace command)
3.5.3 (Scorpion)
- Documentation updates
- Fix in copying the vcf files for the concordance check
3.5.2 (Rhino)
- added GavinStandAlone to the NGS_DNA repo
- updated docs
- tiny bugs in the dependencies in the workflow
- bugfix in GenderCalculate, when there is noChrX it will produces an error due to missing initialisation of a variable
- Gavin output will be outputted in compressed format due to issues with downstream analysis
3.5.1 (Quetzal)
MAJOR BUGFIX
MarkDuplicates: lanes from same sample are merged instead of per lane
new:
-
first version of CartegeniaTree (NOT IN USE by diagnostics)
-
Determine trio's (using VCFped, https://github.com/magnusdv/VCFped)
-
using vcfanno for annotation of the variants (https://github.com/brentp/vcfanno/releases) (Field names are between round brackets)
- CADD (CADD_SCALED, CADD)
- ExAC (EXAC_AF, EXAC_AC_HET, EXAC_AC_HOM)
- gnomAD gnomAD_Hom, gnomAD_Hemi, gnomAD_AN, gnomAD_exome_AF_MAX, gnomAD_exome_RF_Filter,EXAC_AF)
- CGD CGD_Condition, CGD_Inheritance, CGD_AgeGroup, CGD_Manfest_cat, CGD_invent_cat, invent_rat)
- GoNL (GoNL_AC, GoNL_AN)
- Clinvar (clinvar_dn, clinvar_isdb, clinvar_hgvs, clinvar_sig)
-
new version of GAVIN (https://github.com/molgenis/gavin-plus/releases)
- CGD_26jun2018.txt.gz
- clinvar.vkgl.patho.26june2018.vcf.gz
- FDR_allGenes_r1.2.tsv
- GAVIN_calibrations_r0.5.tsv
updated tools
- SnpEff/4.3t-Java-1.8.0_74
- multiqc/1.6
- gavin-plus/1.5.0-Java-1.8.0_74
- ngs-utils/18.06.2
- BCFtools/1.6-foss-2015b
new tools:
vcfanno/v0.2.9
updates:
- created folder that can be picked up by ChronQC for long time statistics
- removing rejected samples out of samplesheet ( if samples will be rejected this will be mailed to mailing group)
- added cram index file
- added single read functionality
- some data will be moved directly to resultsfolder (bam,cram,fastqc,gVCF)
3.4.4 (Pelican)
updated
- docs
- changed prm/cluster for diagnostics
- decreased resources used in some protocols
- removed unused workflows (gonl/hmf)
- removed crashing the pipeline on the genderCheck, now instead it will drop an email and the gender that is calculated will be the "truth" while continuining the pipeline
- added coverage check, when more than 10% of the targets are below 20x coverage, the sample will be rejected (writing to ${sampleNameID}.rejected )
- added check if bedfile exists
bugfixes
- CopyToResultsDir: copying rejectedSamples => misplaced quote
- removed FIFO pipe in prepareFastQ step since this sometimes occurs in an error
3.4.3 (Okapi)
Added:
-
GeneNetwork annotation step
-
new QCReport (MultiQC)
-
MantaAnnotation
-
included track and trace in header and footer
-
panels and exomes can now be in one project
-
fixing phiX concordance check
3.4.2 (Nightingale)
-
Updated data staging prm->tmp in NGS_DNA and removed this from NGS_Automated.
-
updated test (is now testing for both external_samples as in-house samples)
-
added startFromVcf part to the pipeline
NGS_DNA 3.4.1 (Mandrill)
- created trackNtrace header/footer + removal of cutadapt in PrepareFastQ
- fix for not having a vcf index issue
- removing EBROOTSAMBAMBA since it is added to the PATH
- added gender check alarm when samplesheet says e.g. Male and calculated gender is Female
- changing output in PrepareFastQ step since it has storage issues when deploying multiple big jobs
- added M&M part to QCReport
- added set -eu to first rocket
- changed generate_template (it will now work with named arguments)