filmov
tv
subset vcfs
0:02:14
subset vcf by sample names | bcftools view tutorial
0:05:00
Split or Subset VCF files based on Sample IDs using bcftools shortclip
0:46:00
BCFTOOLS view | BCFTOOLS split | Split or Subset VCF files based on Sample IDs
0:03:47
filtering vcfs based on quality | bcftools filter episode1
0:36:17
BCFTools Tutorial for Splitting VCFs based on Sample IDs | BCFTools view Example
0:25:40
Understanding File Formats in Bioinformatics: VCF and gVCF
0:16:50
A bioinformatics tutorial on how to merge multiple vcfs using bcftools
0:23:23
bcftools tutorial on How to read VCF files | Extract and view chromosome names
0:07:37
Bcftools tutorial on How to read VCF files | indexing VCFs
0:45:33
BCFTOOLS Tutorial | How I Extract information from a vcf file
0:22:50
Read VCF files with Python Pandas | Python for Bioinformatics
0:05:54
Extract sample ids from a vcf file using vcftools | episode 1
0:16:11
How to Filter High Quality Variants using BCFTOOLS | VCF files
0:12:46
How to read any VCF file using bcftools tutorial | Bioinformatics for Beginners | Course
0:06:18
Converting Plink format to VCF using Reference genome
0:00:35
SPLIT VCF PROGRAM
0:07:50
Bcftools tutorial | bcftools Split a VCF file into snps and indels
0:02:24
Split a VCF file into snps and indels using bcftools shortclip
0:25:31
bcftools view | bcftools query | Extract sample ids from vcf files using bcftools
0:05:59
Reading VCF data
0:12:43
bcftools query command | Extract and view chromosome names in a VCF file
0:02:58
How to Separate Contacts from VCF File Format?
0:19:10
5 genomics file formats you must know
0:17:22
BCFTOOLS Tutorial | How to Rename Samples in a VCF file using Bcftools reheader command
Вперёд