Epigenetics service

The GENOM'IC core facility offers library preparation and sequencing services for epigenetics projects, using DNA fragments obtained from ChIP, ATAC, CUT&Run or CUT&Tag experiments.

Our service only includes the steps downstream of the extraction of fragments of interest, i.e. from DNA that has already been isolated. The cellular steps (fixation, lysis, immunoprecipitation or tagmentation) must be carried out by the teams.

Our service includes:

🔹 Library preparation from isolated DNA fragments.

🔹 High-throughput sequencing on NextSeq Illumina (depth according to requirements).

Each project is discussed in advance with the facility to define the most appropriate experimental and/or bioinformatics strategy.

For all enquiries, please contact us at: u1016-genomique@inserm.fr

 

Strategies for your epigenetics needs

Here is an overview of the different options for your epigenetics projects:

ChIPseq project:

The requesting team is responsible for preparing the immunoprecipitated DNA. GENOM'IC takes care of preparing the libraries using Diagenode's MicroPlex kit. We then perform paired-end sequencing with a number of reads adapted to the target you are studying (transcription factor, histone marks, etc.).

ATACseq project:

The requesting team can provide us with either isolated DNA fragments after tagmentation or pre-prepared libraries. The samples will be sequenced in paired-end mode with 50 million reads per sample.

CUT&Run or CUT&Tag project:

The team can provide us with previously isolated fragments or entrust us with libraries prepared by them. The samples will be sequenced in paired-end mode, with a number of reads varying from 2 to 10 million per sample.


Do you have questions about the strategy to adopt for your project? Feel free to contact us to discuss it!


Bioinformatic data analysis

We offer a comprehensive range of standard and advanced analyses, including:

  •     Quality control of reads (FastQC, MultiQC).
  •     Sequence alignment to the reference genome with Bowtie2.
  •     Peak calling with MACS3.
  •     Peak annotation by ChIPseeker (proximity to genes, regulatory regions, etc.).
  •     Functional analysis (Gene Ontology, pathway enrichment) on request with clusterProfiler.
  •     Differential peak analysis (comparison between conditions) with Diffbind.
  •     Optional motif discovery.

Each project is discussed in advance with the facility to define the most appropriate experimental and bioinformatics strategy.

For all enquiries, please contact the platform at:

u1016-genomique@inserm.fr


What if our services do not cover your bioinformatics needs? You can contact the BIOINFORMAT'IC core facility at any time to discuss this!