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analyse-seqs
Use when analyzing equal-length sequence sets with the legacy ViennaRNA statistical-geometry, clustering, or distance-matrix utility driven from stdin.
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 analyzing equal-length sequence sets with the legacy ViennaRNA statistical-geometry, clustering, or distance-matrix utility driven from stdin.
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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| name | analyse-seqs |
| description | Use when analyzing equal-length sequence sets with the legacy ViennaRNA statistical-geometry, clustering, or distance-matrix utility driven from stdin. |
| disable-model-invocation | true |
| user-invocable | true |
Legacy ViennaRNA sequence-set analysis tool for equal-length inputs. It reads sequence blocks from stdin, can build Hamming or edit-distance matrices, and can emit PostScript summaries for statistical geometry or tree reconstruction modes.
AnalyseSeqs/home/vimalinx/miniforge3/envs/bio/bin/AnalyseSeqsAnalyseSeqs -h@ or %# 1) Neighbour-joining with Hamming distance and taxa labels
cat <<'EOF' | AnalyseSeqs -Xn -DH
* demo
1 : A
2 : B
3 : C
4 : D
*
AAAA
AAAT
AATT
TTTT
@
EOF
# 2) Statistical geometry (the default -Xb mode) with a PostScript sidecar
cat <<'EOF' | AnalyseSeqs -Xb -DH
* demo
1 : A
2 : B
3 : C
4 : D
*
AAAA
AAAT
AATT
TTTT
@
EOF
# writes demo_box.ps
# 3) Ward clustering with a generated PostScript tree
cat <<'EOF' | AnalyseSeqs -Xw -DH
* demo
1 : A
2 : B
3 : C
4 : D
*
AAAA
AAAT
AATT
TTTT
@
EOF
# writes demo_wards.ps
@ or %.* prefix, followed by numbered n : Taxon lines and a closing *.-X... and the distance algorithm with -D...; use -d... only when you intentionally want a non-default edit-cost matrix.*_box.ps, *_nj.ps, or *_wards.ps.AnalyseSeqs, not analyse-seqs.-h, --help, and --version all fell through to the same usage text in live testing; no clean version banner was observed.@ or %, ignores unrelated non-sequence lines, and supports an optional taxa list beginning with *.AAAA, AAAT, @) exited 0 with no stdout or sidecar output, so do not expect every input size to yield a direct report.-DA and -DG as higher-risk legacy paths.demo_box.ps, demo_nj.ps, and demo_wards.ps.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.