Supplementary Material 3 lists long non-coding RNA-associated somatic mutations identified in non-small cell lung cancer (NSCLC) samples. Each row represents a single mutation observed in one sample, with columns for hg38 genomic coordinates, reference and alternate alleles, allelic fractions, and affected lncRNAs. The 91.5 KB CSV file was authored by Pablo Martin-Lopez and last updated on 2026-04-11 under a CC-BY-4.0 license.
Use Cases
- Identify potential diagnostic biomarkers based on lncRNA mutation patterns in NSCLC.
- Correlate specific genomic coordinates and allelic fractions with clinical outcomes.
- Prioritize therapeutic targets by analyzing mutations in long non-coding RNAs.
Strengths
- Data includes specific hg38 genomic coordinates and allelic fractions for each mutation.
- The dataset is focused on a specific cancer type (NSCLC) and genetic feature (lncRNA mutations).
- Released under a permissive CC-BY-4.0 license for reuse.
Limitations
- Row count is unknown, which may limit suitability assessment.
- Column-level documentation is absent; field semantics must be inferred after download.
- The 91.5 KB file size suggests a limited scope of data.
Provenance
- Source
- Pablo Martin-Lopez via figshare.
- Collection Method
- Likely derived from genomic sequencing of NSCLC patient samples.
- Freshness
- Last updated 2026-04-11 03:36:55; freshness should be verified.