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Comment:
Comment: keep samples that carry non-reference allele in list of variants snpeff/snpsift
2.9 years ago by
curious
▴ 820
3
votes
4
replies
1.3k
views
keep samples that carry non-reference allele in list of variants snpeff/snpsift
snpeff
snpsift
bcftools
2.9 years ago by
curious
▴ 820
0
votes
1
reply
869
views
subset vcf to keep only samples heterozygous or homozygous for the alternate allele of a given variant
bcftools
updated 2.9 years ago by
cfos4698
★ 1.1k • written 2.9 years ago by
curious
▴ 820
1
vote
1
reply
1.6k
views
Answer:
Answer: Haploview.jar
3.0 years ago by
curious
▴ 820
0
votes
0
replies
3.9k
views
Comment:
Comment: Applying Machine Learning on vcf file
3.1 years ago by
curious
▴ 820
1
vote
0
replies
1.6k
views
Answer:
Answer: New datasets for ancestry estimation and imputation?
3.2 years ago by
curious
▴ 820
1
vote
1
reply
884
views
inner merge vcfs in one step?
bcftools
updated 3.2 years ago by
Pierre Lindenbaum
164k • written 3.2 years ago by
curious
▴ 820
0
votes
1
reply
3.9k
views
Comment:
Comment: Applying Machine Learning on vcf file
3.2 years ago by
curious
▴ 820
0
votes
0
replies
538
views
Is it possible to report the allele frequency of integer copy numbers >= 3?
cn.mops
cnv
3.3 years ago by
curious
▴ 820
2
votes
1
reply
635
views
how to get exon regions for this gene w/ build 19 coordinates
bed
updated 3.3 years ago by
GenoMax
148k • written 3.3 years ago by
curious
▴ 820
1
vote
0
replies
2.5k
views
Answer:
Answer: Snakemake bwa mem
3.3 years ago by
curious
▴ 820
0
votes
0
replies
1.1k
views
Answer:
Answer: What is the best software for "phasing" in human population genomics with trio f
3.3 years ago by
curious
▴ 820
0
votes
2
replies
1.6k
views
Comment:
Comment: is local ancestry inference typically always run w/ array genotypes instead of
3.4 years ago by
curious
▴ 820
1
vote
4
replies
1.6k
views
is local ancestry inference typically always run w/ array genotypes instead of imputed genotypes?
ancestry
updated 3.4 years ago by
LauferVA
4.5k • written 3.4 years ago by
curious
▴ 820
0
votes
0
replies
1.0k
views
Comment:
Comment: RFMix v2 - ancestry per individual marker
3.4 years ago by
curious
▴ 820
2
votes
7
replies
2.8k
views
How do I log into this ftp server and look around?
ftp
updated 3.4 years ago by
Mensur Dlakic
★ 28k • written 3.4 years ago by
curious
▴ 820
0
votes
0
replies
2.8k
views
Comment:
Comment: How do I log into this ftp server and look around?
3.4 years ago by
curious
▴ 820
0
votes
2
replies
2.8k
views
Comment:
Comment: How do I log into this ftp server and look around?
3.4 years ago by
curious
▴ 820
0
votes
0
replies
3.4k
views
Comment:
Comment: Highly used R packages with no Python equivalent
3.4 years ago by
curious
▴ 820
0
votes
0
replies
548
views
is it possible to subset samples and reheader a vcf in a single step?
bcftools
3.4 years ago by
curious
▴ 820
0
votes
0
replies
908
views
can you use LD scores from build 37 reference to get LD score intercept on build 38 summary stats?
ld
regression
score
3.4 years ago by
curious
▴ 820
0
votes
2
replies
6.8k
views
Comment:
Comment: sorting a multi-sample (genotype) vcf file
3.5 years ago by
curious
▴ 820
4
votes
2
replies
1.9k
views
You can't just liftover from one build to another using only coordinates correct?
liftover
updated 3.5 years ago by
darink
▴ 10 • written 4.0 years ago by
curious
▴ 820
0
votes
0
replies
2.3k
views
Comment:
Comment: what pihat cutoffs from plink --genome are 3rd degree relative
3.6 years ago by
curious
▴ 820
1
vote
1
reply
2.3k
views
what pihat cutoffs from plink --genome are 3rd degree relative
related
ibd
plink
3.6 years ago by
curious
▴ 820
0
votes
1
reply
1.3k
views
Comment:
Comment: Make map file with recombination rate using plink?
3.6 years ago by
curious
▴ 820
0
votes
3
replies
1.3k
views
Make map file with recombination rate using plink?
germline
plink
updated 3.6 years ago by
4galaxy77
2.9k • written 3.6 years ago by
curious
▴ 820
0
votes
0
replies
927
views
Comment:
Comment: how to identify haplotypes and its frequency based SNP genotyping data?
3.6 years ago by
curious
▴ 820
0
votes
0
replies
657
views
Comment:
Comment: Does this output indicate my bam is paired end?
3.7 years ago by
curious
▴ 820
1
vote
2
replies
657
views
Does this output indicate my bam is paired end?
samtools
3.7 years ago by
curious
▴ 820
2
votes
0
replies
2.6k
views
Answer:
Answer: How to connect HLA alleles with rsID?
3.7 years ago by
curious
▴ 820
0
votes
1
reply
1.1k
views
Comment:
Comment: Could someone help me check what genomic position is this variant nomenclature r
3.7 years ago by
curious
▴ 820
1
vote
5
replies
1.1k
views
Could someone help me check what genomic position is this variant nomenclature referring to ?
nomeclature
updated 3.7 years ago by
cpad0112
21k • written 3.7 years ago by
curious
▴ 820
0
votes
0
replies
3.6k
views
Answer:
Answer: how to run linux code in python
3.7 years ago by
curious
▴ 820
0
votes
0
replies
1.4k
views
Comment:
Comment: quick way to get samples that are NOT homozygous reference for a given record us
3.7 years ago by
curious
▴ 820
0
votes
1
reply
1.4k
views
Comment:
Comment: quick way to get samples that are NOT homozygous reference for a given record us
3.7 years ago by
curious
▴ 820
0
votes
4
replies
1.4k
views
quick way to get samples that are NOT homozygous reference for a given record using bcftools?
bcftools
3.7 years ago by
curious
▴ 820
0
votes
0
replies
762
views
Does a smaller value of F from PLINK --het represent higher heterozygosity?
plink
3.7 years ago by
curious
▴ 820
0
votes
0
replies
520
views
is the absolute value of `plink2.eigenvec.var` from `plink2 --pca biallelic-var-wts approx` a measure of how much each SNP drives PCS?
plink
3.7 years ago by
curious
▴ 820
0
votes
1
reply
849
views
Is there any way to access the --cores argument in a snakemake workflow?
snakemake
updated 2.9 years ago by
Eugene A
▴ 190 • written 3.8 years ago by
curious
▴ 820
0
votes
0
replies
1.0k
views
Comment:
C: STAR alignment loop segmentation fualt (core dumped)
3.8 years ago by
curious
▴ 820
0
votes
0
replies
1.4k
views
Comment:
C: How do I organize snakemake when not all jobs successfully output files from pre
3.8 years ago by
curious
▴ 820
0
votes
0
replies
853
views
Answer:
A: Hardy-Weinberg equilibrium and GWAS in a livestock species (advice)
3.8 years ago by
curious
▴ 820
3
votes
3
replies
1.0k
views
how to use unix tools to convert VCF genotypes like '1|1' to this '2'
bcftools
unix
updated 18 months ago by
Ram
44k • written 3.8 years ago by
curious
▴ 820
0
votes
0
replies
1.0k
views
Comment:
C: how to use unix tools to convert VCF genotypes like '1|1' to this '2'
3.8 years ago by
curious
▴ 820
1
vote
1
reply
743
views
"SNP" record in vcf looks like this: 6:28035427:GTA:ATA ?
vcf
3.9 years ago by
curious
▴ 820
0
votes
0
replies
2.6k
views
Comment:
C: Merging WGS SNP array data
3.9 years ago by
curious
▴ 820
0
votes
0
replies
1.3k
views
Is this an OK approach for lifting over a mixture of b36 & b37 to b38 variants using rsids only?
liftover
3.9 years ago by
curious
▴ 820
0
votes
1
reply
2.6k
views
Comment:
C: Merging WGS SNP array data
3.9 years ago by
curious
▴ 820
1
vote
1
reply
2.6k
views
Comment:
C: Merging WGS SNP array data
3.9 years ago by
curious
▴ 820
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