bcftools/filter.h at develop · samtools/bcftools · GitHub
The evaluation of Bcftools mpileup and GATK HaplotypeCaller for variant calling in non-human species | Scientific Reports
First steps in genomic data analysis - Evolution and Genomics
Variant Calling using BCFtools
教程】如何使用BCFtools提取全基因组数据到芯片模拟数据？ - 知乎
CallSNPs.py - wiki
IJMS | Free Full-Text | Multiple Variant Calling Pipelines in Wheat Whole Exome Sequencing
bcftools view maf filter · Issue #357 · samtools/bcftools · GitHub
5. Variant calling and visualization — Physalia Paleogenomics 0.1.0 documentation
PDF) How to extract and filter SNP data from the genotyping-by- sequencing (GBS) data in vcf format using bcftools
Cells | Free Full-Text | A Next Generation Sequencing-Based Protocol for Screening of Variants of Concern in Autism Spectrum Disorder
BCFtools filter - Issue with DP and basic question · Issue #1209 · samtools/ bcftools · GitHub
Filtering of VCF Files
RPubs - Part 2. NGS data analysis-BCF tools
Filtering of VCF Files
bcftools filter -e 'GT="het"' recognize GT 2/2 as heterozygous · Issue #1268 · samtools/bcftools · GitHub
The evaluation of Bcftools mpileup and GATK HaplotypeCaller for variant calling in non-human species | Scientific Reports
Variant Calling with BCFTOOLS | Galaxy Tutorial - YouTube
A simple SNP calling pipeline
vcf_filter.py: VCF Filter Function — PPP 0.1.13 documentation
How to filter with formated INFO fields? · Issue #1340 · samtools/bcftools · GitHub
7. Variant calling — Genomics Tutorial 2020.2.0 documentation
processing vcfs with bcftools episode 1 - YouTube
