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comments
0
votes
0
replies
1.4k
views
Comment:
Comment: drop duplicate insertion deletions in VCF at same position while keeping one
2.8 years ago by
curious
▴ 900
2
votes
1
reply
1.5k
views
In GWAS what is the point of regressing a quantitative phenotype on covariates first and taking the residuals?
gwas
updated 2.8 years ago by
LChart
5.1k • written 2.8 years ago by
curious
▴ 900
1
vote
1
reply
907
views
calculating the allele frequency of a gene deletion and duplication
cnv
updated 2.8 years ago by
German.M.Demidov
★ 3.0k • written 2.8 years ago by
curious
▴ 900
5
votes
11
replies
4.3k
views
fast way to get last position in a large indexed VCF?
bcftools
updated 3.1 years ago by
Istvan Albert
103k • written 3.1 years ago by
curious
▴ 900
0
votes
1
reply
4.3k
views
Comment:
Comment: fast way to get last position in a large indexed VCF?
3.1 years ago by
curious
▴ 900
0
votes
1
reply
4.3k
views
Comment:
Comment: fast way to get last position in a large indexed VCF?
3.1 years ago by
curious
▴ 900
0
votes
0
replies
1.4k
views
Comment:
Comment: is it possible to calculate MAF from DS instead of GT when using bcftools +fill-
3.2 years ago by
curious
▴ 900
0
votes
0
replies
1.4k
views
Comment:
Comment: is it possible to calculate MAF from DS instead of GT when using bcftools +fill-
3.2 years ago by
curious
▴ 900
0
votes
3
replies
1.4k
views
is it possible to calculate MAF from DS instead of GT when using bcftools +fill-tags?
bcftools
3.2 years ago by
curious
▴ 900
1
vote
0
replies
808
views
Does genomic control have a valid interpretation when there are no genome-wide significant hits
genomic
control
statistics
3.3 years ago by
curious
▴ 900
0
votes
0
replies
747
views
am I understanding scaled CADD scores correct?
cadd
3.5 years ago by
curious
▴ 900
2
votes
1
reply
900
views
Using snpsift to filter VCF by sample
snpsift
updated 3.5 years ago by
Pierre Lindenbaum
166k • written 3.5 years ago by
curious
▴ 900
0
votes
0
replies
689
views
Does larger standardized PRS value always means higher risk?
prs
3.6 years ago by
curious
▴ 900
0
votes
0
replies
2.2k
views
Comment:
Comment: grep a vcf
3.7 years ago by
curious
▴ 900
0
votes
0
replies
936
views
Converting observed heritability to liability scale, how to get standard error?
hertiability
greml
ldsc
3.7 years ago by
curious
▴ 900
0
votes
0
replies
1.8k
views
Comment:
Comment: keep samples that carry non-reference allele in list of variants snpeff/snpsift
3.8 years ago by
curious
▴ 900
0
votes
1
reply
1.8k
views
Comment:
Comment: keep samples that carry non-reference allele in list of variants snpeff/snpsift
3.8 years ago by
curious
▴ 900
3
votes
4
replies
1.8k
views
keep samples that carry non-reference allele in list of variants snpeff/snpsift
snpeff
snpsift
bcftools
3.8 years ago by
curious
▴ 900
0
votes
1
reply
1.2k
views
subset vcf to keep only samples heterozygous or homozygous for the alternate allele of a given variant
bcftools
updated 3.8 years ago by
cfos4698
★ 1.2k • written 3.8 years ago by
curious
▴ 900
1
vote
1
reply
2.1k
views
Answer:
Answer: Haploview.jar
3.9 years ago by
curious
▴ 900
0
votes
0
replies
4.9k
views
Comment:
Comment: Applying Machine Learning on vcf file
3.9 years ago by
curious
▴ 900
1
vote
0
replies
2.2k
views
Answer:
Answer: New datasets for ancestry estimation and imputation?
4.0 years ago by
curious
▴ 900
1
vote
1
reply
1.2k
views
inner merge vcfs in one step?
bcftools
updated 4.0 years ago by
Pierre Lindenbaum
166k • written 4.0 years ago by
curious
▴ 900
0
votes
1
reply
4.9k
views
Comment:
Comment: Applying Machine Learning on vcf file
4.0 years ago by
curious
▴ 900
0
votes
0
replies
746
views
Is it possible to report the allele frequency of integer copy numbers >= 3?
cn.mops
cnv
4.1 years ago by
curious
▴ 900
2
votes
1
reply
876
views
how to get exon regions for this gene w/ build 19 coordinates
bed
updated 4.2 years ago by
GenoMax
154k • written 4.2 years ago by
curious
▴ 900
1
vote
0
replies
3.3k
views
Answer:
Answer: Snakemake bwa mem
4.2 years ago by
curious
▴ 900
0
votes
0
replies
1.5k
views
Answer:
Answer: What is the best software for "phasing" in human population genomics with trio f
4.2 years ago by
curious
▴ 900
0
votes
2
replies
2.0k
views
Comment:
Comment: is local ancestry inference typically always run w/ array genotypes instead of
4.2 years ago by
curious
▴ 900
1
vote
4
replies
2.0k
views
is local ancestry inference typically always run w/ array genotypes instead of imputed genotypes?
ancestry
updated 4.2 years ago by
LauferVA
4.8k • written 4.2 years ago by
curious
▴ 900
0
votes
0
replies
1.3k
views
Comment:
Comment: RFMix v2 - ancestry per individual marker
4.2 years ago by
curious
▴ 900
2
votes
7
replies
3.8k
views
How do I log into this ftp server and look around?
ftp
updated 4.2 years ago by
Mensur Dlakic
★ 30k • written 4.2 years ago by
curious
▴ 900
0
votes
0
replies
3.8k
views
Comment:
Comment: How do I log into this ftp server and look around?
4.2 years ago by
curious
▴ 900
0
votes
2
replies
3.8k
views
Comment:
Comment: How do I log into this ftp server and look around?
4.2 years ago by
curious
▴ 900
0
votes
0
replies
4.6k
views
Comment:
Comment: Highly used R packages with no Python equivalent
4.2 years ago by
curious
▴ 900
0
votes
0
replies
715
views
is it possible to subset samples and reheader a vcf in a single step?
bcftools
4.3 years ago by
curious
▴ 900
0
votes
0
replies
1.2k
views
can you use LD scores from build 37 reference to get LD score intercept on build 38 summary stats?
ld
regression
score
4.3 years ago by
curious
▴ 900
0
votes
2
replies
8.2k
views
Comment:
Comment: sorting a multi-sample (genotype) vcf file
4.4 years ago by
curious
▴ 900
4
votes
2
replies
2.4k
views
You can't just liftover from one build to another using only coordinates correct?
liftover
updated 4.4 years ago by
darink
▴ 10 • written 4.8 years ago by
curious
▴ 900
0
votes
0
replies
2.8k
views
Comment:
Comment: what pihat cutoffs from plink --genome are 3rd degree relative
4.4 years ago by
curious
▴ 900
1
vote
1
reply
2.8k
views
what pihat cutoffs from plink --genome are 3rd degree relative
related
ibd
plink
4.4 years ago by
curious
▴ 900
0
votes
1
reply
1.7k
views
Comment:
Comment: Make map file with recombination rate using plink?
4.4 years ago by
curious
▴ 900
0
votes
3
replies
1.7k
views
Make map file with recombination rate using plink?
germline
plink
updated 4.4 years ago by
4galaxy77
2.9k • written 4.4 years ago by
curious
▴ 900
0
votes
0
replies
1.4k
views
Comment:
Comment: how to identify haplotypes and its frequency based SNP genotyping data?
4.5 years ago by
curious
▴ 900
0
votes
0
replies
948
views
Comment:
Comment: Does this output indicate my bam is paired end?
4.5 years ago by
curious
▴ 900
1
vote
2
replies
948
views
Does this output indicate my bam is paired end?
samtools
4.5 years ago by
curious
▴ 900
2
votes
0
replies
3.3k
views
Answer:
Answer: How to connect HLA alleles with rsID?
4.5 years ago by
curious
▴ 900
0
votes
1
reply
1.6k
views
Comment:
Comment: Could someone help me check what genomic position is this variant nomenclature r
4.5 years ago by
curious
▴ 900
1
vote
5
replies
1.6k
views
Could someone help me check what genomic position is this variant nomenclature referring to ?
nomeclature
updated 4.5 years ago by
cpad0112
21k • written 4.5 years ago by
curious
▴ 900
0
votes
0
replies
4.5k
views
Answer:
Answer: how to run linux code in python
4.5 years ago by
curious
▴ 900
316 results • Page
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