An open-access platform to discover transcription factor binding sites, quantify binding affinities, and compare regulations across the human genome.
Decode Regulation. Drive Discovery.
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ENTIRE is designed to span the full spectrum of transcription factors (TFs) across the human genome, enabling systematic insights into their regulatory mechanisms. It is constructed based on our newly-developed in vitro FOOtprinting with DeamInasE (ivtFOODIE) technique, which is a variation from previously developed FOODIE. FOODIE stands for FOOtprinting with DeamInasE, and is a technique that delineates transcription factor binding sites genome-wide with near–single-base precision, at single-molecule and single-cell resolution.
ivtFOODIE is a high-throughput sequencing-based technique that quantitatively measures equilibrium dissociation constants (Kd) for TFs across the accessible human genome. By using cytosine deaminase footprinting at near–single-base resolution and titrating TF concentrations, ivtFOODIE determines Kd values on thousands of natural genomic binding sites in a simple in vitro setup, offering a powerful foundation for decoding gene-regulatory networks.
Seq2Kd is a deep-learning framework that predicts TF-DNA binding affinities for any TF on any DNA sequence. It combines large-scale pre-training on public motif datasets such as JASPAR and HOCOMOCO with fine-tuning on experimentally measured affinities by ivtFOODIE. Seq2Kd generalizes across TF families and quantifies how disease-related SNVs alter TF binding strength, bridging experimental biophysics with genome-wide prediction. Using the Seq2Kd tool, users are able to estimate TF–DNA binding affinity as an equilibrium dissociation constant (Kd) for any given set of DNA and amino acid sequences.
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