Identify, locate and analyse Putative G-Quadruplex and i-Motif forming sequences across genes, promoters, and regulatory regions — directly in your browser.
Scans genes and sequences for Putative G-Quadruplex forming Sequences (PGS) using G₃₊(N₁₋₇)G₃₊(N₁₋₇)G₃₊(N₁₋₇)G₃₊ pattern recognition across promoter, gene body, and 3′ downstream regions. Fetches live genomic data via Ensembl REST API.
Scans genes and sequences for Putative i-Motif forming Sequences (PIS) using C₃₊(N₁₋₇)C₃₊(N₁₋₇)C₃₊(N₁₋₇)C₃₊ pattern recognition. Intercalated motifs form on the complementary strand to G-Quadruplexes, playing crucial roles in gene regulation and chromatin architecture.
Submit a list of gene symbols or Ensembl IDs — separated by line or comma — and QuaDB will sequentially query Ensembl, fetch all three genomic regions, and report PGS counts and sequences for every gene in a single run. Ideal for pathway-level or genome-wide screens.
Run i-Motif screening across an entire gene panel simultaneously. Input your gene list, select an organism, and receive a structured report showing PIS counts across all three genomic regions for every gene — in one click.
Enter a gene symbol (e.g. MYC, TERT, BRCA1), Ensembl ID, or paste a raw FASTA sequence directly.
QuaDB queries the Ensembl REST API in real-time, pulling promoter (−1 kb), gene body, and 3′ downstream (+1 kb) sequences.
Regex-based pattern matching identifies all PGS/PIS, each scored by a G/C-tract depth and loop composition algorithm.
Results rendered as an interactive distribution map and annotated table. Export to TXT for downstream analysis.