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comments
0
votes
0
replies
677
views
Comment:
Comment: Merging gvcf files between Dragen and other calling tools
4 months ago by
tacrolimus
▴ 150
0
votes
1
reply
677
views
Comment:
Comment: Merging gvcf files between Dragen and other calling tools
5 months ago by
tacrolimus
▴ 150
0
votes
4
replies
677
views
Merging gvcf files between Dragen and other calling tools
gvcf
merge
bcftools
4 months ago by
tacrolimus
▴ 150
1
vote
0
replies
1.3k
views
Comment:
Comment: Factors affecting the size of a structural variant
23 months ago by
tacrolimus
▴ 150
0
votes
0
replies
1.3k
views
Comment:
Comment: Factors affecting the size of a structural variant
23 months ago by
tacrolimus
▴ 150
9
votes
5
replies
1.3k
views
Factors affecting the size of a structural variant
CNV
SV
23 months ago by
tacrolimus
▴ 150
4
votes
0
replies
1.3k
views
Answer:
Answer: Factors affecting the size of a structural variant
23 months ago by
tacrolimus
▴ 150
1
vote
0
replies
709
views
Forum:
Penetrance versus heritability
penetrance
heritability
2.3 years ago by
tacrolimus
▴ 150
1
vote
0
replies
650
views
Meta-analysis of rare variant SAIGE-GENE output for WGS data
meta-analysis
rare
SAIGE
variant
2.4 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.1k
views
Comment:
Comment: Counting the specific number of a type of variant per sample in a multi-sample
2.4 years ago by
tacrolimus
▴ 150
5
votes
3
replies
1.1k
views
Counting the specific number of a type of variant per sample in a multi-sample VCF
bcftools
VCF
updated 2.4 years ago by
Pierre Lindenbaum
166k • written 2.4 years ago by
tacrolimus
▴ 150
0
votes
0
replies
944
views
Comment:
Comment: Ascertaining whether polygenic risk score is statistically independent to a mono
2.6 years ago by
tacrolimus
▴ 150
4
votes
2
replies
944
views
Ascertaining whether polygenic risk score is statistically independent to a monogenic risk
polygenic
score
PRS
risk
SAIGE
2.6 years ago by
tacrolimus
▴ 150
3
votes
1
reply
855
views
Pathway analysis using rare-variant SKAT-O summary statistics
variant
rare
pathway
analysis
R
updated 2.6 years ago by
LChart
5.0k • written 2.6 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.2k
views
Comment:
Comment: Basic PRS question
2.7 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.2k
views
Comment:
Comment: Basic PRS question
2.7 years ago by
tacrolimus
▴ 150
0
votes
4
replies
1.2k
views
Basic PRS question
PRS
2.7 years ago by
tacrolimus
▴ 150
0
votes
0
replies
885
views
Running a validated polygenic risk score (PRS) on a new dataset using VCF/PGEN files (in the 100K genomes project)
PRS
polygenic
risk
score
2.8 years ago by
tacrolimus
▴ 150
0
votes
2
replies
2.1k
views
Counting allele counts/frequencies from a vcf file with both cases and controls
bcftools
allele count
vep
updated 3.3 years ago by
Paolo
• 0 • written 4.8 years ago by
tacrolimus
▴ 150
0
votes
0
replies
824
views
Answer:
Answer: Ancient DNA Analysis Fastq to vcf
3.4 years ago by
tacrolimus
▴ 150
0
votes
0
replies
791
views
Power calculation for a collapsing rare variant analysis
calculation
SAIGE
power
rare
variant
collapsing
test
3.4 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.8k
views
Comment:
Comment: Creating a per sample file from multi-sample vcf
3.6 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.8k
views
Comment:
Comment: Creating a per sample file from multi-sample vcf
3.6 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.8k
views
Comment:
Comment: Creating a per sample file from multi-sample vcf
3.6 years ago by
tacrolimus
▴ 150
4
votes
5
replies
1.8k
views
Creating a per sample file from multi-sample vcf
bcftools
SNV
SNP
vcftools
vcf
3.6 years ago by
tacrolimus
▴ 150
4
votes
1
reply
796
views
Pulling out "alts" from a multisample vcf by sample ID - bcftools syntax question
bcftools
vcf
3.7 years ago by
tacrolimus
▴ 150
3
votes
0
replies
796
views
Answer:
Answer: Pulling out "alts" from a multisample vcf by sample ID - bcftools syntax questio
3.7 years ago by
tacrolimus
▴ 150
0
votes
0
replies
605
views
Bioinformatic interrogation of non-coding variants in gVCFs
VCF
gVCF
non-coding
3.9 years ago by
tacrolimus
▴ 150
0
votes
0
replies
629
views
Best way of visualising genetic variation for publication in a gene with many exons
graphs
snv
lollipop
snp
Visualisation
3.9 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.4k
views
Comment:
Comment: Count number of occurrences an annotation in a multisample vcf split into multip
3.9 years ago by
tacrolimus
▴ 150
4
votes
2
replies
1.4k
views
Count number of occurrences an annotation in a multisample vcf split into multiple chunks
bcftools
vcf
annotation
3.9 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.4k
views
Split Y-Axis of a manhattan plot in qqman (using R)
manhattan
R
genomics
4.0 years ago by
tacrolimus
▴ 150
0
votes
0
replies
2.4k
views
Comment:
C: Extract samples with alternative genotype from a multi-sample VCF
4.5 years ago by
tacrolimus
▴ 150
0
votes
0
replies
2.4k
views
Comment:
C: Extract samples with alternative genotype from a multi-sample VCF
4.5 years ago by
tacrolimus
▴ 150
0
votes
4
replies
2.4k
views
Extract samples with alternative genotype from a multi-sample VCF
vcf
bcftools
vep
updated 4.5 years ago by
abascalfederico
★ 1.2k • written 4.5 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.3k
views
Adding SNP/Gene labels to a qqplot using qqman
qqman
qqplot
gwas
R
4.6 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.5k
views
locuszoom on a HPC - LD could not be computed for SNP
locuszoom
HPC
bash
GWAS
4.6 years ago by
tacrolimus
▴ 150
0
votes
0
replies
2.2k
views
Comment:
C: Filtering large VCFs by allele freqency using bcftools split-vep function
4.6 years ago by
tacrolimus
▴ 150
1
vote
0
replies
2.0k
views
Comment:
C: Finding unique variants by sample ID in a multisample vcf
4.7 years ago by
tacrolimus
▴ 150
6
votes
2
replies
2.0k
views
Finding unique variants by sample ID in a multisample vcf
bcftools
vcf
SNP
vep
updated 4.7 years ago by
brunobsouzaa
▴ 840 • written 4.7 years ago by
tacrolimus
▴ 150
0
votes
0
replies
922
views
Leveraging phenotype data in rare variant and GWAS analysis
SNP
genome
phenotype
GWAS
rare variant
4.9 years ago by
tacrolimus
▴ 150
0
votes
0
replies
2.8k
views
Comment:
C: Faster filtering of vcfs using split-vep over filter_vep
updated 5.3 years ago by
finswimmer
16k • written 5.3 years ago by
tacrolimus
▴ 150
0
votes
1
reply
2.0k
views
Answer:
A: Extract several columns from a VCF file
updated 5.3 years ago by
Ram
45k • written 5.3 years ago by
tacrolimus
▴ 150
0
votes
0
replies
2.0k
views
Comment:
A: Extract several columns from a VCF file
5.3 years ago by
tacrolimus
▴ 150
1
vote
2
replies
2.8k
views
Faster filtering of vcfs using split-vep over filter_vep
VEP
bcftools
split-vep
vcf
5.3 years ago by
tacrolimus
▴ 150
3
votes
12
replies
1.9k
views
BCFTOOLS: One-liner to get individuals with more than one heterozygote call in a region
bcftools
5.3 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.9k
views
Comment:
C: BCFTOOLS: One-liner to get individuals with more than one heterozygote call in a
5.3 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.9k
views
Comment:
C: BCFTOOLS: One-liner to get individuals with more than one heterozygote call in a
5.3 years ago by
tacrolimus
▴ 150
0
votes
0
replies
1.9k
views
Comment:
C: BCFTOOLS: One-liner to get individuals with more than one heterozygote call in a
5.3 years ago by
tacrolimus
▴ 150
0
votes
1
reply
1.9k
views
Comment:
C: BCFTOOLS: One-liner to get individuals with more than one heterozygote call in a
5.3 years ago by
tacrolimus
▴ 150
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