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4
votes
3
replies
1.5k
views
where to find GRCh38 for 1000 Genomes
VCF GRCh38 1000Genomes
updated 3.1 years ago by 11k • written 3.2 years ago by ▴ 100
9
votes
6
replies
4.1k
views
where can i find the GRCh38 genetic map for IMPUTE2
map GRCh38 IMPUTE2
3.1 years ago by raalsuwaidi ▴ 100
0
votes
0
replies
420
views
How does IMPUTE2 calculate concordance
concordance IMPUTE2
3.2 years ago by raalsuwaidi ▴ 100
2
votes
3
replies
1.0k
views
How to perform imputation analysis between masked SNPs and ground truth
GWAS SNPs IMPUTE2
updated 3.2 years ago by 4.7k • written 3.3 years ago by ▴ 100
0
votes
0
replies
537
views
How to calculate r2 for IMPUTE2
r2 IMPUTE2
3.3 years ago by raalsuwaidi ▴ 100
6
votes
6
replies
1.6k
views
how to remove positions in VCF based on rsID
vcf plink bcftools
updated 23 months ago by 45k • written 3.3 years ago by ▴ 100
0
votes
0
replies
502
views
How does IMPUTE2 assigns snp_id
SNP VCF IMPUTE2 bcftools PLINK
3.3 years ago by raalsuwaidi ▴ 100
3
votes
1
reply
2.1k
views
how to convert from hap/legend to VCF
-merge_ref_panels_output_ref VCF IMPUTE2
updated 3.3 years ago by 11k • written 3.3 years ago by ▴ 100
1
vote
4
replies
1.7k
views
how to loop and select values from a python dataframe
dataframe python
3.3 years ago by raalsuwaidi ▴ 100
2
votes
1
reply
1.2k
views
understand and how to plot the PLINK mdist file
plink mdist plot
3.4 years ago by raalsuwaidi ▴ 100
0
votes
2
replies
1.4k
views
help with CrossMap
VCF hg38 hg19 CrossMap
3.3 years ago by raalsuwaidi ▴ 100
7
votes
2
replies
3.9k
views
struggling in using bcftools to set variants to missing
missing2ref setGT bcftools vcf
updated 2.3 years ago by • 0 • written 3.5 years ago by ▴ 100
0
votes
0
replies
565
views
map files
genome impute2 map
3.5 years ago by raalsuwaidi ▴ 100
0
votes
0
replies
584
views
IMPUTE2 -merge_ref_panels output
IMPUTE2
3.6 years ago by raalsuwaidi ▴ 100
0
votes
0
replies
683
views
Distance matrix PCA
HAP PCA distance
3.6 years ago by raalsuwaidi ▴ 100
3
votes
9
replies
2.6k
views
IMPUTE2 -merge_ref_panels
IMPUTE2 -merge_ref_panels
updated 3.7 years ago by 89k • written 3.7 years ago by ▴ 100
1
vote
2
replies
996
views
custom reference panel
sample impute GWAS
3.7 years ago by raalsuwaidi ▴ 100
3
votes
4
replies
2.5k
views
color coded PCA plot in R for a combined set
plink pca plot
3.8 years ago by raalsuwaidi ▴ 100
3
votes
4
replies
1.7k
views
PCA for combined set
plink bcftools vcf PCA
3.9 years ago by raalsuwaidi ▴ 100
1
vote
2
replies
849
views
Combining two vcf files
Vcf GWAS
3.9 years ago by raalsuwaidi ▴ 100
0
votes
0
replies
775
views
Combining data sets for PCA
Plink 1000genome PCA genotype
3.9 years ago by raalsuwaidi ▴ 100
4
votes
4
replies
1.9k
views
setting genotypes to missing
genotype vcf impute
3.9 years ago by raalsuwaidi ▴ 100
1
vote
2
replies
1.2k
views
missing REF and ALT in vcf
REF SNP VCF ALT
3.9 years ago by raalsuwaidi ▴ 100
4
votes
7
replies
2.1k
views
Mask a SNP before imputation
genotype bcftools impute2 mask VCF
3.7 years ago by raalsuwaidi ▴ 100
1
vote
1
reply
1.1k
views
two allele frequency
allele position BCFTOOLS
updated 4.1 years ago by 14k • written 4.1 years ago by ▴ 100
0
votes
0
replies
688
views
error when imputing for mismatch legend file
impute2 haps shapeit legend
4.1 years ago by raalsuwaidi ▴ 100
0
votes
2
replies
1.4k
views
VCF rare variants and exon
vcf exon rare variants
5.1 years ago by raalsuwaidi ▴ 100
0
votes
3
replies
1.5k
views
IMPUTE2 variable question
vcf impute2 imputation
updated 5.1 years ago by 89k • written 5.1 years ago by ▴ 100
7
votes
5
replies
1.3k
views
what does ./1 in a VCF file means
vcf genome snp sequence
updated 5.1 years ago by ▴ 970 • written 5.1 years ago by ▴ 100
29 results • Page 1 of 1
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