用 Codex 或 Claude 帮你安装 复制这段 Prompt,粘贴到 Codex、Claude 或其他助手里,让它检查 Skill 页面并帮你完成安装。
直接命令不会经过审查 Prompt;运行前请先检查来源。
npx skills add https://github.com/vimalinx/bio-agent --skill vcftools命令会保持在同一行。复制前请横向滚动并检查完整内容。
想先保存到本地?可下载 SkillsMP 当前能够提供的文件。
基于 SOC 职业分类
正在显示 SKILL.md
| name | vcftools |
| description | Use when working with Variant Call Format (VCF) files and need to filter, summarize, or manipulate variant data. |
| disable-model-invocation | true |
| user-invocable | true |
vcftools/home/vimalinx/miniforge3/envs/bio/bin/vcftools/home/vimalinx/miniforge3/envs/bio/share/man/man1/vcftools.1vcftools for classic population-genetics style filtering and quick summaries.# 1) SNP-only filtered VCF
vcftools \
--gzvcf cohort.vcf.gz \
--remove-indels \
--recode --recode-INFO-all \
--out cohort.snps_only
# 2) Common-variant, low-missingness filter
vcftools \
--gzvcf cohort.vcf.gz \
--maf 0.05 \
--max-missing 0.9 \
--recode --recode-INFO-all \
--out cohort.filtered
# 3) Allele-frequency report for one chromosome
vcftools \
--gzvcf cohort.vcf.gz \
--freq \
--chr 1 \
--out chr1.freq
# 4) Site mean depth summary
vcftools \
--gzvcf cohort.vcf.gz \
--site-mean-depth \
--out cohort.depth
--vcf, --gzvcf, or --bcf.--recode and usually --recode-INFO-all.--out is omitted, files default to the out.* prefix in the current directory.--recode writes a new VCF; without it many filtering commands only emit summary files.--max-missing 1.0 keeps only sites with no missing genotypes, which is often much harsher than intended.