Diese Seite ist nur auf Englisch verfügbar.

Core Facility – DEEPSEQ Deep Sequencing Facility

The Deep Sequencing Core Facility was established in September 2010 to provide the Neuenheimer Feld Campus with access to Next Generation Sequencing (NGS). We provide the possibility to construct libraries for sequencing with the focus not only on the „standard“ application but on the establishment of custom protocols which can be of benefit to the entire campus.

Sequencing is available on a variety of instruments all based on the Illumina Sequencing by Synthesis technology, i.e. NGS Library Preparation or Single Cell Library Preparation for 10x Chromium NGS Sequencing. In addition to library preparation and sequencing we also help with planning sequencing experiments and offer advice on projects.

Logo: an abstract and minimal dna string in light blue lies over the text: “deep sequencing” in black bold letters and under that “facility” in light blue bold letters

Project requests

All researchers from Heidelberg University and the Health + Life Science Alliance Heidelberg Mannheim are welcome to request help or place orders for Next Generation Sequencing analyses. Projects funded through company funding unfortunately cannot be accepted.

Deep Seq Timeline with the steps: First contact, research plan, online request, sample submission, lab work, anlalysis results

Before sample submission please:

  • follow the steps of our sample submission guide with specified requirements for different sample types (download document).
  • read carefully the iLabs sample registration guideline (download document)
  • see our end-user license agreement (EULA; download PDF) for more general information on the Deep Sequencing Core Facility's services as well as users' rights and duties. New customers are requested to bring a signed copy of the EULA when submitting the first sample set.

Sample registration   

Services & Equipment

SERVICES

  • NGS Library Preparation (Illumina Platform)
    • Bulk RNA library preparation (poly-A capture, rRNA and/or globin depletion, tagmentation)
    • Small RNA library preparation
    • ChIP-seq
    • gDNA library preparation (de novo or resequencing)
    • Target enrichment
  • Single-cell library preparation (10X Genomics and Parse Biosciences)
  • Spatial transcriptomics library preparation (10X Genomics Visium, Visium HD). 
  • NGS Sequencing (Illumina Platform)

    We accommodate, after discussion with staff, custom protocols brought by users.

EQUIPMENT

  • Illumina MiniSeq (22-25 million reads output)
  • Illumina NextSeq 2000 (100 million to 1.8 billion reads output)
  • In collaboration with EMBL: Pacbio and Oxford Nanopore (EMBL GeneCore)
  • 10X Genomics Chromium X
  • 10X Genomics CytAssist
  • Covaris S2 Sonicator
  • Agilent Bioanalyzer 2100

Team

Tabelle

Portrait of a man who smiles

David Ibberson

Head of Facility

Deep Sequencing Lab BQ 40
BioQuant
INF 267
69120 Heidelberg

Office: +49 6221 54 51359 / Rm 001
Lab: +49 6221 54 51369 / Rm 606 / U27

david.ibberson@bioquant.uni-heidelberg.de

A portrait of a woman with glasses who smiles

Bianka Berki , PhD

NGS and Spatial Omics Specialist

bianka.berki@bioquant.uni-heidelberg.de

Group contact email:

Selected publications

Tabelle

Funding Resources

4 Logos are displayed: Health &Lifescence alliance, Multispace platform, University of heidelberg, COS - Center for organismal studies