Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : questions
0
votes
3
replies
482
views
read 012 matrix
vcftools
updated 8 months ago by 40k • written 8 months ago by • 0
0
votes
4
replies
659
views
how to deal with missing genotype data (gt) to do a machine learning
missing_data
updated 8 months ago by ★ 2.9k • written 8 months ago by • 0
0
votes
0
replies
285
views
snpmatix for multi allelic
snpmatrix
9 months ago by arwa.ahmad95 • 0
0
votes
4
replies
793
views
bcftools view remove (.) id
bcftools
11 months ago by arwa.ahmad95 • 0
0
votes
3
replies
537
views
Extract specific variants from vcf to annotate
vcf
updated 11 months ago by 40k • written 11 months ago by • 0
0
votes
2
replies
372
views
Annotation for specific id ( not all )
annotation
11 months ago by arwa.ahmad95 • 0
0
votes
3
replies
449
views
seperate vcf file to multiple files based on samples
seperate
written 15 months ago by • 0
1
vote
4
replies
674
views
meaning of genotype
vcf genotype
15 months ago by arwa.ahmad95 • 0
0
votes
0
replies
264
views
choose databbases in variant annotation
annotate Annovar
16 months ago by arwa.ahmad95 • 0
0
votes
2
replies
494
views
annotate vcf file
annovar annotation
19 months ago by arwa.ahmad95 • 0
0
votes
3
replies
785
views
filter and annotate vcf file
vcf annotate filter
updated 19 months ago by 26k • written 19 months ago by • 0
0
votes
5
replies
744
views
VariantsToTable not produce output file
VariantsToTable GATK
19 months ago by arwa.ahmad95 • 0
0
votes
1
reply
628
views
genotype matrix
structure python
updated 2.5 years ago by ▴ 280 • written 2.5 years ago by • 0
13 results • Page 1 of 1
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6