TFscope




Characterizing the binding preferences of transcription factors (TFs) in different cell types and conditions is key to understand how they orchestrate gene expression. TFscope is a machine learning approach that identifies sequence features explaining the binding differences observed between two ChIP-seq experiments targeting either the same TF in two conditions or two TFs with similar motifs (paralogous TFs). TFscope systematically investigates differences in the core motif, nucleotide environment and co-factor motifs, and provides the contribution of each key feature in the two experiments.


TFscope online execution

Input data
Drag and drop a file or click to browse.
No file selected
BED file for the first class (Chip1).
Drag and drop a file or click to browse.
No file selected
BED file for the second class (Chip2).
Drag and drop a file or click to browse.
No file selected
Genome FASTA file.
Drag and drop a file or click to browse.
No file selected
Motif collection in MEME format (.meme).
Parameters
Identifier of the targeted motif in the MEME file (ex. MA0007.1). Optional.
Base pairs added upstream and downstream in peaks to find the best occurrence.
Base pairs added upstream and downstream in the motif (DM).
Number of bins in lattice (DExTER and TFscope).
P-value threshold for FIMO when scanning motifs.
Sets of sequences to compare.
TFscope TFscope TFscope online

RSCU_RS: Measuring the bias in codon usage from ribosomal activity

RSCU_RS: Measuring the bias in…

Overview Overview: In the protein coding sequences of a species, the 61 possible codons of the genetic code are not equally distributed. This observation is referred to as the Codon Usage Bias (CUB) of a species. Several measures have been proposed to quantify the CUB using the frequencies of codons in all RNA coding sequences…

Bioinformatics Comparative genomics Computational biology Codon usage analysis Codon usage bias Expression data RNA sequence BAM
FastME 2.0

FastME 2.0

FastME is a software package for the fast and accurate inference of phylogenetic trees from distance matrices. It implements algorithms based on the Balanced Minimum Evolution (BME) principle, a distance-based criterion closely related to the Neighbor Joining (NJ) method. The goal of the BME framework is to identify the phylogenetic tree that minimizes the total…

MYST

MYST

What is MYST? MYST is the orchestration platform behind ATGC online bioinformatics services. It provides a unified web interface and a public REST API to submit analyses, monitor jobs, and retrieve results across a growing catalog of phylogenetic and sequence-analysis tools. TIDE is a modernized redesign of WAVES, an older tool previously developped by ATGC…

Sequence analysis Software engineering Service discovery Service invocation Service management Job identifier Tool metadata HTML JSON
⚠️ Online tool executions will be unavailable on June 16, 2026, from 9:00 AM due to scheduled cluster maintenance. ⚠️ This website is under construction, some information or links could be unavailable ⚠️