Showing: vcfreset
<prev • 1,512 results • page 1 of 51 • next >
1
vote
1
answer
88
views
1
answer
LiftOver a VCF file
vcf liftovervcf crossmap picard written 1 day ago by Susmita Mandal0 • updated 1 day ago by RamRS17k
0
votes
0
answers
52
views
0
answers
Hapmap to vcf
vcf hapmap convert written 2 days ago by shinken12360 • updated 1 day ago by RamRS17k
0
votes
0
answers
62
views
0
answers
4
votes
0
answers
86
views
0
answers
8
votes
2
answers
160
views
2
answers
Replace symbols in R table
vcf R gsub written 6 days ago by Inquisitive899520 • updated 5 days ago by Santosh Anand3.9k
2
votes
1
answer
183
views
1
answer
1
vote
0
answers
77
views
0
answers
2
votes
1
answer
188
views
1
answer
How to calculate Minor Allele Frequency (MAF) for your own population data
vcf maf written 11 days ago by Sudhir Jadhao60 • updated 11 days ago by Kevin Blighe28k
2
votes
1
answer
109
views
1
answer
2
votes
1
answer
92
views
1
answer
Parameter to filter a VCF of SNPs?
vcf parameters snp written 13 days ago by Picasa380 • updated 13 days ago by RamRS17k
0
votes
0
answers
99
views
0
answers
2
votes
1
answer
147
views
1
answer
faster variant annotation for large VCFs
vcf wgs variant annotation written 17 days ago by Amitm1.6k • updated 17 days ago by Emily_Ensembl15k
0
votes
0
answers
76
views
0
answers
0
votes
0
answers
162
views
0
answers
R or Python code for pairwise genetic identity from a VCF file
vcf R next-gen snp python written 24 days ago by Stephanie0 • updated 21 days ago by Biostar ♦♦ 20
0
votes
1
answer
75
views
1
answer
2
votes
1
answer
163
views
1
answer
Gene based counts in scikit-allel
vcf python scikit-allel written 26 days ago by danaUM0 • updated 26 days ago by alimanfoo20
0
votes
0
answers
111
views
0
answers
0
votes
0
answers
156
views
0
answers
31
votes
3
answers
353
views
12 follow
3
answers
Fast way to extract part of genotypes data from 1000 Genome VCF files
fast vcf 1000genome written 4 weeks ago by Shicheng Guo6.5k • updated 29 days ago by chrchang5233.9k
2
votes
1
answer
100
views
1
answer
1000 genome project - difference between "0" and "0|0"
vcf genotype 1000 genome project written 4 weeks ago by mbk0asis380 • updated 4 weeks ago by Santosh Anand3.9k
2
votes
1
answer
179
views
1
answer
Merge vcf files of structural variants
vcf merge structural_variants written 4 weeks ago by ma170 • updated 4 weeks ago by WouterDeCoster32k
0
votes
1
answer
145
views
1
answer
VCF to Bed file format using GATK
vcf gatk rna-seq bed written 5 weeks ago by Sa0 • updated 5 weeks ago by chrchang5233.9k
0
votes
0
answers
185
views
0
answers
How group merged VCFs in one GT column
vcf bcftools written 5 weeks ago by miqrom0 • updated 5 weeks ago by Kevin Blighe28k
6
votes
1
answer
161
views
1
answer
snps/indels with individual genotypes from 1000 genomes ftp site
vcf 1000 genomes genotypes ftp written 5 weeks ago by lait120 • updated 5 weeks ago by Kevin Blighe28k
2
votes
1
answer
183
views
1
answer
Variant Allele Frequency
vcf samtools snp written 5 weeks ago by kspata30 • updated 5 weeks ago by btsui260
2
votes
0
answers
180
views
0
answers
Error when indexing a bcf file
vcf bcf written 5 weeks ago by Fersal10
2
votes
0
answers
204
views
5 follow
0
answers
0
votes
0
answers
141
views
0
answers
0
votes
1
answer
305
views
1
answer
VCF filtering based on AB (Allele-Balance) tag
vcf allele balance written 6 weeks ago by AISHA40 • updated 6 weeks ago by RamRS17k
0
votes
1
answer
133
views
1
answer
No output estimating LD between SNPs in VCF using PLINK
vcf plink written 6 weeks ago by GabrielMontenegro410 • updated 6 weeks ago by Kevin Blighe28k
<prev • 1,512 results • page 1 of 51 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 726 users visited in the last hour