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NGS short reads sequencing (Illumina)

NGS short reads sequencing (Illumina)

Custom preparation, validation and sequencing of DNA and RNA libraries.

Applications

Genome and amplicon sequencing
Genomic & epigenetic editing: Chip-seq
Transcriptome sequencing: RNA-seq
MicroRNome sequencing: small RNA-seq, Mime-seq
Ribosome profiling: Ribo-seq
Microbiome sequencing: 16S-rRNA-seq

Throughput

Up to 50 million paired-end reads
Maximum sequencing length: 1 x 600 cycles or 2 x 300 cycles in 56 hours
Up to 15 Gb of data
Custom multiplexing

How to submit a project to the platform?

To submit a project to the AEG platform, contact us by email at aeg@ibmp-cnrs.unistra.fr

We will propose a preparation meeting to define the best strategy to adopt and the technological approach to consider. An estimate of the costs and delays will then be established. The deadline for carrying out the experiments will be communicated to you after validation of the samples. In some cases, an exchange with a bioinformatician will be offered to you before the launch of the project.

Form and pricing

For each project, please fill out the project request form and the sample description_form.