issues
search
Clinical-Genomics
/
raredisease
CG's rare disease pipeline in next flow, see the main repo here 👇
https://github.com/nf-core/raredisease
MIT License
5
stars
1
forks
source link
issues
Newest
Newest
Most commented
Recently updated
Oldest
Least commented
Least recently updated
Missing annotated STR call VCF - in HK?
#24
dnil
opened
1 week ago
5
Naming of SMNCopyNumberCall tsv
#23
dnil
opened
1 week ago
0
Mastermind
#22
dnil
opened
1 week ago
1
MARRVELAI - Should we have it?
#21
fulyataylan
opened
1 month ago
2
Overzealous html escapes in VCF?
#20
dnil
closed
1 month ago
1
Use bwa-mem instead of bwa-mem2 if bwa-mem2 fails twice
#19
rannick
opened
2 months ago
0
Config file fails with error when submitting job through cg run.
#18
peterpru
closed
3 months ago
3
Empty ME VCFs
#17
dnil
closed
3 months ago
1
MIssing autozygosity tracks for chromograph
#16
jemten
closed
4 months ago
1
ExHu/Stranger VCF unsplit
#15
dnil
closed
4 months ago
2
SMNcopynumbercaller tsv sample names
#14
dnil
closed
4 months ago
1
NGSbits output compatibility
#13
jemten
opened
5 months ago
0
Add mobile element calling into the pipeline
#12
peterpru
closed
5 months ago
1
Add in analysis of CYP21A2?
#11
KickiLagerstedt
opened
8 months ago
5
Change pLI score to o/e
#10
jemten
opened
1 year ago
0
Tools for detection of variants in near-coding regions
#9
fulyataylan
opened
2 years ago
1
Make shared reference folder to test full pipeline
#8
projectoriented
opened
2 years ago
0
Java memory issue on SLURM
#2
jemten
closed
1 year ago
7
Annotating 5'UTRs
#3
fulyataylan
opened
2 years ago
4
Add config for local cluster
#1
jemten
closed
2 years ago
1
Newish problematic assembly quality tracks from UCSC
#5
dnil
closed
2 years ago
1
Evaluate dbMTS
#6
henrikstranneheim
closed
2 years ago
1
gnomAD MNV
#4
dnil
opened
5 years ago
2
Evaluate uORF VEP plugin
#7
genecracker
closed
2 years ago
2