65/100 (Medium)

OpenClaw： suspicious
VirusTotal： benign
StaticScan： clean

OpenClaw： suspicious

The skill's description promises full CNV calling and plotting from WGS, but the shipped code is a minimal placeholder that does not implement real CNV algorithms — mismatch suggests this is a prototy...

[内容已截断]

VirusTotal： benign VT 报告

静态扫描： clean

No suspicious patterns detected.

README 未提供

{
    "latestVersion": {
        "_creationTime": 1773806033569,
        "_id": "k979g4jzvhhmbfqgefes55gged83586d",
        "changelog": "Initial release of cnv-caller-plotter, enabling CNV detection and visualization from WGS data:\n\n- Detects copy number variations (CNVs) from whole genome sequencing (WGS) data for cancer, rare disease, and population genomics.\n- Supports input formats including BAM and VCF, with genomic segmentation and customizable bin sizes.\n- Exports CNV calls in standard BED format for downstream analysis.\n- Generates publication-quality genome-wide CNV visualization plots in PNG, PDF, or SVG.\n- Integrates with other bioinformatics skills for upstream QC and downstream analysis\/visualization.",
        "changelogSource": "auto",
        "createdAt": 1773806033569,
        "version": "0.1.0"
    },
    "owner": {
        "_creationTime": 0,
        "_id": "publishers:missing",
        "displayName": "AIpoch",
        "handle": "aipoch-ai",
        "image": "https:\/\/avatars.githubusercontent.com\/u\/258999481?v=4",
        "kind": "user",
        "linkedUserId": "kn76fcc8jhxekae91m2ekbrsgn821avs"
    },
    "ownerHandle": "aipoch-ai",
    "skill": {
        "_creationTime": 1773806033569,
        "_id": "kd7d0znvwajaws92k6mdsged15835rz6",
        "badges": [],
        "createdAt": 1773806033569,
        "displayName": "Cnv Caller Plotter",
        "latestVersionId": "k979g4jzvhhmbfqgefes55gged83586d",
        "ownerUserId": "kn76fcc8jhxekae91m2ekbrsgn821avs",
        "slug": "cnv-caller-plotter",
        "stats": {
            "comments": 0,
            "downloads": 47,
            "installsAllTime": 0,
            "installsCurrent": 0,
            "stars": 0,
            "versions": 1
        },
        "summary": "Detect copy number variations from whole genome sequencing data and generate publication-quality genome-wide CNV plots. Supports CNV calling, segmentation, a...",
        "tags": {
            "latest": "k979g4jzvhhmbfqgefes55gged83586d"
        },
        "updatedAt": 1774336769355
    }
}