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 spdi2tbl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。
Use when joint-genotyping one or more germline gVCFs into a cohort VCF with GATK GenotypeGVCFs.
Use when running GATK HaplotypeCaller to emit per-sample germline variant calls or gVCFs from analysis-ready BAM/CRAM inputs.
Use when splitting mixed accession-like text into one lowercase token per line in EDirect-style text pipelines.
基于 SOC 职业分类
正在显示 SKILL.md
| name | spdi2tbl |
| description | Use when flattening SPDI XML records into sorted, deduplicated tabular rows for downstream variant pipelines. |
| disable-model-invocation | true |
| user-invocable | true |
Tiny Bash wrapper around xtract plus a final sort-table | cut | uniq cleanup. It reads <SPDI> XML, emits variant rows with rsID, accession, position, deleted/inserted sequence, class, type, and gene, then sorts and deduplicates the result.
... | spdi2tbl/home/vimalinx/miniforge3/envs/bio/bin/spdi2tblefetch -db snp ... | snp2hgvs | hgvs2spdihgvs2spdi into shell-friendly TSV output# Canonical dbSNP pipeline into a flat table
efetch -db snp -id 104894914 -format docsum | snp2hgvs | hgvs2spdi | spdi2tbl
# Save flattened SPDI rows for downstream use
some_spdi_xml_generator | spdi2tbl > variants.tsv
# Feed directly into tbl2prod
efetch -db snp -id 104894914 -format docsum | snp2hgvs | hgvs2spdi | spdi2tbl | tbl2prod
<SPDI> XML upstream, typically from hgvs2spdi.spdi2tbl.tbl2prod or other shell filters only after confirming the accession/class mix is what you expect.-h and --version fell through to xtract and failed with No data supplied to xtract from stdin or file.Genomic=1, Coding=2, Protein=3 before sorting.sort-table being available on PATH.rs104894914 NC_000023.11 154191715 T C Genomic Substitution OPN1MW.uniq after sorting, so repeated equivalent rows are collapsed silently.