Notch Biallelic Variants Screening Data for Congenital Hypothyroidism

Supplementary materials supporting a large-scale genetic screening study for congenital hypothyroidism. The dataset includes figures, Excel spreadsheets, and other files totaling 127.6 MB. It was authored by Fengyao Wu and published under a CC-BY-4.0 license in 2026.

Use Cases

• Validate reported genetic associations based on supplementary variant data
• Recreate study figures based on provided TIF image files
• Perform secondary analysis on candidate gene lists based on Excel spreadsheet contents

Strengths

• Data directly supports a peer-reviewed publication's findings
• Files are provided in common, accessible formats like XLSX and DOCX

Limitations

• Column-level documentation is absent; field semantics must be inferred after download
• Row count is unknown, which may limit suitability assessment

Provenance

Source

figshare

Freshness

Last updated 2026-05-25 08:26:21