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0
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3
replies
867
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Protocol to combine WGS with Nanopore for Structural Variant confirmation?
wgs
updated 15 months ago by ★ 1.9k • written 16 months ago by ▴ 140
0
votes
0
replies
421
views
Normalisation of PLINK/VCF files?
plink
20 months ago by optimistsso4co3 ▴ 140
1
vote
0
replies
722
views
Answer: Answer: Prediction of T2D, based on GWAS rsIDs
20 months ago by optimistsso4co3 ▴ 140
0
votes
0
replies
644
views
Guide for ICD-10 to EFO conversion?
icd10 efo
21 months ago by optimistsso4co3 ▴ 140
0
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0
replies
1.2k
views
Comment: Comment: Don't see uploaded files for linking in EGA (European Genome Archive)
2.1 years ago by optimistsso4co3 ▴ 140
0
votes
2
replies
1.2k
views
Don't see uploaded files for linking in EGA (European Genome Archive)
EGA
2.1 years ago by optimistsso4co3 ▴ 140
2
votes
1
reply
1.5k
views
How to Remove Phasing Information from a VCF File?
phasing
updated 2.1 years ago by 166k • written 2.1 years ago by ▴ 140
0
votes
1
reply
3.5k
views
Comment: Comment: Singularity image is not working in nextflow
2.2 years ago by optimistsso4co3 ▴ 140
0
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2
replies
3.5k
views
Comment: Comment: Singularity image is not working in nextflow
2.2 years ago by optimistsso4co3 ▴ 140
3
votes
6
replies
3.5k
views
Singularity image is not working in nextflow
nextflow singularity
updated 2.2 years ago by 88k • written 2.2 years ago by ▴ 140
0
votes
0
replies
424
views
Is there a array-based population dataset with phenotypes like eye colour available?
gwas
2.3 years ago by optimistsso4co3 ▴ 140
2
votes
1
reply
769
views
fastQC - how to know if sample is good quality ?
fastqc
updated 2.3 years ago by 45k • written 2.3 years ago by ▴ 140
0
votes
0
replies
635
views
Protocol to detect chromosomal ploidy from WGS VCF?
wgs ploidy
2.4 years ago by optimistsso4co3 ▴ 140
0
votes
2
replies
863
views
Can you apply Base Score Recalibration in parallel?
wgs
updated 2.4 years ago by 5.0k • written 2.4 years ago by ▴ 140
0
votes
1
reply
1.1k
views
Comment: Comment: How to interpret deletion the length of chromosome?
2.4 years ago by optimistsso4co3 ▴ 140
0
votes
3
replies
1.1k
views
How to interpret deletion the length of chromosome?
del
updated 2.4 years ago by 166k • written 2.4 years ago by ▴ 140
0
votes
7
replies
1.6k
views
Is it possible to query column of particular sample on VCF?
vcf
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
1.6k
views
Answer: Answer: Is it possible to query column of particular sample on VCF?
2.9 years ago by optimistsso4co3 ▴ 140
4
votes
6
replies
1.9k
views
How to filter VCF for only variants present in particular sample?
vcf
2.9 years ago by optimistsso4co3 ▴ 140
1
vote
0
replies
1.9k
views
Answer: Answer: How to filter VCF for only variants present in particular sample?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
1.9k
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
1.9k
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
1.9k
views
Answer: Answer: How to filter VCF for only variants present in particular sample?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
1.6k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
1.6k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
1.6k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
2.9 years ago by optimistsso4co3 ▴ 140
1
vote
2
replies
780
views
Is it possible to annotate each person individually with VEP?
VEP
updated 2.9 years ago by 5.0k • written 2.9 years ago by ▴ 140
1
vote
1
reply
707
views
Is there a tool to standartise ANY kind of human variant list file? (like vcf, plink, 23andMe etc)
23andme
updated 2.9 years ago by 2.9k • written 2.9 years ago by ▴ 140
0
votes
1
reply
809
views
Where to find Structural variant database dgvMerged for ANNOVAR?
annovar
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
809
views
Answer: Answer: Where to find Structural variant database dgvMerged for ANNOVAR?
2.9 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
523
views
How to control number of cores GATK can use?
gatk
3.0 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
1.3k
views
Comment: Comment: Research Scientist (Fungal & Algal Program)
3.1 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
702
views
Do you have to select "pulled" or "final" bam in MELT mobile element discovery step of genotyping?
melt
updated 4 months ago by • 0 • written 3.1 years ago by ▴ 140
0
votes
0
replies
885
views
Comment: Comment: Mobile element discovery with MELT brings different results when chromosomes are
3.1 years ago by optimistsso4co3 ▴ 140
0
votes
2
replies
885
views
Mobile element discovery with MELT brings different results when chromosomes are analysed separate
melt
3.1 years ago by optimistsso4co3 ▴ 140
1
vote
1
reply
1.1k
views
Is it possible to add variant type "VT" to each variant in vcf?
bcftools
updated 3.1 years ago by 45k • written 3.1 years ago by ▴ 140
0
votes
3
replies
923
views
gatk requests enormous amounts of memory. How to limit it?
gatk
updated 3.1 years ago by ▴ 840 • written 3.1 years ago by ▴ 140
0
votes
0
replies
616
views
How to extract region from GVCF file?
GVCF
3.2 years ago by optimistsso4co3 ▴ 140
1
vote
1
reply
664
views
How to calculate indels per individual?
vcf
updated 3.4 years ago by 166k • written 3.4 years ago by ▴ 140
1
vote
1
reply
1.4k
views
How to prepare vcf for use with Picard?
picard
updated 3.4 years ago by 166k • written 3.4 years ago by ▴ 140
0
votes
0
replies
577
views
How to fill vcf ALT field for sites where it's missing?
vcf
3.4 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
1.4k
views
Comment: Comment: How to correct for allele frequency mismatches?
3.4 years ago by optimistsso4co3 ▴ 140
2
votes
2
replies
1.4k
views
How to correct for allele frequency mismatches?
plink
3.4 years ago by optimistsso4co3 ▴ 140
6
votes
10
replies
2.4k
views
Why isn't it a common practice to call variant for every position in human genome?
ngs
updated 3.5 years ago by 23k • written 3.5 years ago by ▴ 140
1
vote
0
replies
2.4k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.5 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
2.4k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.5 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
2.4k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.5 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
2.4k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.5 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
756
views
Fastest pipeline for large scale joint genotype calling?
calling
updated 3.6 years ago by 166k • written 3.6 years ago by ▴ 140
0
votes
0
replies
606
views
Is there such thing as GVCF for structural variants allowing population genetics on SVs?
sv
3.6 years ago by optimistsso4co3 ▴ 140
75 results • Page 1 of 2
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