issues
search
NYU-Molecular-Pathology
/
NGS580-nf
Target exome sequencing analysis for NYU NGS580 gene panel
GNU General Public License v3.0
10
stars
5
forks
source link
issues
Newest
Newest
Most commented
Recently updated
Oldest
Least commented
Least recently updated
R installed in home dir breaks Singularity containers
#43
varshini712
opened
4 years ago
2
Remove 'done' channels
#42
stevekm
opened
5 years ago
0
Need to refactor channel `create` method
#41
stevekm
opened
5 years ago
0
Updated samplesheets do not seem to always work correctly with 'resume'
#40
stevekm
opened
5 years ago
0
Sometimes values loaded from JSON are not available inside processes
#39
stevekm
opened
5 years ago
0
Evaluate Nextflow Tower integration
#38
stevekm
opened
5 years ago
0
Need to adjust memory allocation for jobs
#37
stevekm
opened
5 years ago
0
Use full git tag in output tables
#36
stevekm
closed
5 years ago
1
Need output validator
#35
stevekm
opened
5 years ago
0
masked nucleotides showing up in vcf files, breaking merge script
#34
stevekm
closed
5 years ago
0
Need to include `finalize-work-rm` in with default `run` Makefile recipe
#33
stevekm
closed
5 years ago
0
Refactor variant calling processes to use separate normalize_vcf steps
#32
stevekm
opened
5 years ago
0
LoFreq Somatic output include dbSNP variants
#31
stevekm
closed
5 years ago
0
rename karyotype plots
#30
stevekm
opened
5 years ago
0
Need scope writeup
#29
stevekm
opened
5 years ago
0
re-setup vaf distribution plot
#28
stevekm
opened
5 years ago
0
Need to update coverage cutoffs
#27
stevekm
opened
5 years ago
0
sometimes custom analysis report does not run
#26
stevekm
opened
5 years ago
2
need bash trap for .nextflow.submitted
#25
stevekm
closed
5 years ago
2
Errors in `reformat-vcf-table.py` return exit code 0
#24
stevekm
opened
5 years ago
2
Need to refactor pairs channels to include 'callerType'
#23
stevekm
closed
5 years ago
0
Need writeup for CNV Pool reference file generation workflow
#22
stevekm
opened
5 years ago
0
remove process lofreq_filter_reformat from config
#21
stevekm
opened
5 years ago
0
Need karyotype plot
#20
stevekm
closed
5 years ago
0
Need to refactor LoFreq and HaplotypeCaller to use separate filter and tsv processes
#19
stevekm
closed
5 years ago
0
Need to update TMB calculation methods for pairs, unpaired samples
#18
stevekm
closed
5 years ago
0
Need to run genomic signatures for all variant callers
#17
stevekm
closed
5 years ago
0
Add CNVKit targets annotation file creation method
#16
stevekm
closed
5 years ago
1
Add configs for different targets.bed files
#15
stevekm
closed
5 years ago
0
Add subdirs to publishDirs for .bam files
#14
stevekm
closed
5 years ago
1
Need to refactor variable name in cnvkit process
#13
stevekm
closed
5 years ago
0
resume not working with RealignerTargetCreator step
#12
stevekm
closed
5 years ago
1
Fix failed tumor-normal comparison log in report
#11
stevekm
closed
5 years ago
1
need to refactor reference file staging methods
#10
stevekm
closed
5 years ago
2
need to update ref download methods
#9
stevekm
closed
5 years ago
1
docker build error
#8
hmkim
closed
5 years ago
6
filter for fastq with no reads
#7
stevekm
closed
5 years ago
3
add FACETS to pipeline
#6
stevekm
closed
5 years ago
0
split bam_ra_rc_gatk process
#5
stevekm
closed
5 years ago
0
Need to support deployment with multiple fastq directories
#4
stevekm
closed
6 years ago
1
Update QC report metrics
#3
stevekm
closed
5 years ago
1
Make 'no lane split' default for samplesheet via deployment setup
#2
stevekm
closed
6 years ago
1
copy samplesheet to output dir
#1
stevekm
closed
5 years ago
0