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bam-to-bed
Use when converting BAM alignment files to BED6, BED12, or BEDPE format for downstream analysis or visualization.
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。
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Use when converting BAM alignment files to BED6, BED12, or BEDPE format for downstream analysis or visualization.
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。
基于 SOC 职业分类
| name | bam-to-bed |
| description | Use when converting BAM alignment files to BED6, BED12, or BEDPE format for downstream analysis or visualization. |
| disable-model-invocation | true |
| user-invocable | true |
bamToBed -i input.bam [options] > output.bed/home/vimalinx/miniforge3/envs/bio/bin/bamToBedreferences/help.md-split, -splitD, or -bed12.-bedpe.# 1) Basic BAM to BED6
bamToBed \
-i alignments.bam > alignments.bed
# 2) BED12 output for split alignments
bamToBed \
-i alignments.bam \
-bed12 > alignments.bed12
# 3) BEDPE for paired-end reads
bamToBed \
-i alignments.qname.bam \
-bedpe > alignments.bedpe
-bedpe.-split / -splitD when the CIGAR structure matters for exon-aware or gapped alignments.-bedpe requires BAM records to be grouped or sorted by query.-bed12 forces -split.-splitD also forces -split and breaks on both N and D CIGAR operators.-tag must reference a numeric BAM tag and cannot be combined with BEDPE output.-ed changes that semantics, especially for BEDPE where the mate edit distances are combined.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.
Use when converting ACE assembly files into SAM while preserving legacy ACE-specific padded or contig-sequence behavior.
Use when pretty-printing tab-delimited output with left, center, right, or decimal-aware numeric alignment in EDirect text workflows.
Use when masking columns or coordinate ranges in multiple-sequence alignments before downstream HMMER or alignment-processing steps.