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0
votes
3
replies
636
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Protocol to combine WGS with Nanopore for Structural Variant confirmation?
wgs
updated 10 months ago by ★ 1.9k • written 10 months ago by ▴ 140
0
votes
0
replies
351
views
Normalisation of PLINK/VCF files?
plink
14 months ago by optimistsso4co3 ▴ 140
0
votes
0
replies
534
views
Guide for ICD-10 to EFO conversion?
icd10 efo
15 months ago by optimistsso4co3 ▴ 140
0
votes
2
replies
957
views
Don't see uploaded files for linking in EGA (European Genome Archive)
EGA
20 months ago by optimistsso4co3 ▴ 140
2
votes
1
reply
1.2k
views
How to Remove Phasing Information from a VCF File?
phasing
updated 20 months ago by 164k • written 20 months ago by ▴ 140
3
votes
6
replies
2.8k
views
Singularity image is not working in nextflow
nextflow singularity
updated 21 months ago by 86k • written 21 months ago by ▴ 140
0
votes
0
replies
356
views
Is there a array-based population dataset with phenotypes like eye colour available?
gwas
22 months ago by optimistsso4co3 ▴ 140
2
votes
1
reply
663
views
fastQC - how to know if sample is good quality ?
fastqc
updated 22 months ago by 44k • written 22 months ago by ▴ 140
0
votes
0
replies
546
views
Protocol to detect chromosomal ploidy from WGS VCF?
wgs ploidy
23 months ago by optimistsso4co3 ▴ 140
0
votes
2
replies
731
views
Can you apply Base Score Recalibration in parallel?
wgs
updated 23 months ago by 4.7k • written 23 months ago by ▴ 140
0
votes
3
replies
949
views
How to interpret deletion the length of chromosome?
del
updated 24 months ago by 164k • written 24 months ago by ▴ 140
0
votes
7
replies
1.3k
views
Is it possible to query column of particular sample on VCF?
vcf
2.5 years ago by optimistsso4co3 ▴ 140
4
votes
6
replies
1.6k
views
How to filter VCF for only variants present in particular sample?
vcf
2.5 years ago by optimistsso4co3 ▴ 140
1
vote
2
replies
670
views
Is it possible to annotate each person individually with VEP?
VEP
updated 2.5 years ago by 4.7k • written 2.5 years ago by ▴ 140
1
vote
1
reply
585
views
Is there a tool to standartise ANY kind of human variant list file? (like vcf, plink, 23andMe etc)
23andme
updated 2.5 years ago by 2.9k • written 2.5 years ago by ▴ 140
0
votes
1
reply
686
views
Where to find Structural variant database dgvMerged for ANNOVAR?
annovar
2.5 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
466
views
How to control number of cores GATK can use?
gatk
2.6 years ago by optimistsso4co3 ▴ 140
0
votes
0
replies
530
views
Do you have to select "pulled" or "final" bam in MELT mobile element discovery step of genotyping?
melt
2.6 years ago by optimistsso4co3 ▴ 140
0
votes
2
replies
767
views
Mobile element discovery with MELT brings different results when chromosomes are analysed separate
melt
2.6 years ago by optimistsso4co3 ▴ 140
1
vote
1
reply
879
views
Is it possible to add variant type "VT" to each variant in vcf?
bcftools
updated 2.7 years ago by 44k • written 2.7 years ago by ▴ 140
0
votes
3
replies
755
views
gatk requests enormous amounts of memory. How to limit it?
gatk
updated 2.7 years ago by ▴ 840 • written 2.7 years ago by ▴ 140
0
votes
0
replies
535
views
How to extract region from GVCF file?
GVCF
2.7 years ago by optimistsso4co3 ▴ 140
1
vote
1
reply
545
views
How to calculate indels per individual?
vcf
updated 3.0 years ago by 164k • written 3.0 years ago by ▴ 140
1
vote
1
reply
1.3k
views
How to prepare vcf for use with Picard?
picard
updated 3.0 years ago by 164k • written 3.0 years ago by ▴ 140
0
votes
0
replies
515
views
How to fill vcf ALT field for sites where it's missing?
vcf
3.0 years ago by optimistsso4co3 ▴ 140
2
votes
2
replies
1.1k
views
How to correct for allele frequency mismatches?
plink
3.0 years ago by optimistsso4co3 ▴ 140
6
votes
10
replies
2.0k
views
Why isn't it a common practice to call variant for every position in human genome?
ngs
updated 3.1 years ago by 23k • written 3.1 years ago by ▴ 140
0
votes
1
reply
685
views
Fastest pipeline for large scale joint genotype calling?
calling
updated 3.1 years ago by 164k • written 3.1 years ago by ▴ 140
0
votes
0
replies
533
views
Is there such thing as GVCF for structural variants allowing population genetics on SVs?
sv
3.1 years ago by optimistsso4co3 ▴ 140
2
votes
1
reply
596
views
How to extract specific location in .bam files
bam
updated 3.1 years ago by 148k • written 3.1 years ago by ▴ 140
0
votes
1
reply
779
views
Is it correct to merge multiple gvcf from separate variant calling?
gatk
updated 3.2 years ago by 23k • written 3.2 years ago by ▴ 140
0
votes
1
reply
858
views
Wha does combineGVCFs does to loci with variant only in gVCF from another analysis?
gatk
3.2 years ago by optimistsso4co3 ▴ 140
0
votes
5
replies
1.4k
views
What are "must have" data types one should extract from WGS .fq data?
wgs
updated 3.2 years ago by 164k • written 3.2 years ago by ▴ 140
6
votes
3
replies
975
views
Is it ok to replace missing WGS calls with reference notation "0/0"?
wgs
updated 3.2 years ago by 164k • written 3.2 years ago by ▴ 140
8
votes
1
reply
4.7k
views
Can someone explain PLINK allele REF/ALT management strategy?
plink
updated 3.2 years ago by 11k • written 3.2 years ago by ▴ 140
2
votes
1
reply
771
views
What is the largest freely available dataset of WGS samples?
wgs
updated 3.2 years ago by ▴ 260 • written 3.2 years ago by ▴ 140
0
votes
1
reply
1.1k
views
How to best predict effect for each variant and count specific effect found in each individual using variant effect predictor?
vcf vep
updated 3.3 years ago by 24k • written 3.3 years ago by ▴ 140
2
votes
5
replies
2.3k
views
How to pass custom software specific variables to nf-core/sarek nextflow pipeline?
wgs
updated 3.4 years ago by ★ 1.4k • written 3.5 years ago by ▴ 140
4
votes
5
replies
1.4k
views
How to paralle trim_galore for single sample?
trim_galore
updated 3.5 years ago by 86k • written 3.5 years ago by ▴ 140
0
votes
0
replies
564
views
What causes highly inflated p values of X chromosome in PLINK association analysis?
plink
4.1 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
1.0k
views
Whats the format for PLINK .set file for epistasis analysis?
plink epistasis .set
updated 4.3 years ago by 11k • written 4.3 years ago by ▴ 140
0
votes
2
replies
836
views
What's the probability of genotype error at the end of 10 repeated A variants? Given low coverage sequencing of 1000G phase 1
sequencing error
4.7 years ago by optimistsso4co3 ▴ 140
0
votes
1
reply
791
views
How to save SNPs removed by quality control? Plink
plink
4.9 years ago by optimistsso4co3 ▴ 140
3
votes
3
replies
1.9k
views
Whats the point of genotype pruning before imputation?
imputation plink --indep-pariwise r2
5.5 years ago by optimistsso4co3 ▴ 140
44 results • Page 1 of 1
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