CF DNA Sequencing

The Facility provides next-generation DNA sequencing (NGS) technology to the FLI. External users may also have access to the technology, e.g. upon collaborative arrangements. In addition to sample DNA/RNA quality check, library preparation and sequencing, the facility provides first-pass data processing, data quality check and analysis. A number of pipelines for deeper data analysis are established and available, also via the CF Life Science Computing of the FLI.

Beyond analyzing whole genomes or subfractions thereof (e.g. exomes), NGS is ideally suited to provide insight into fundamental biological processes, such as transcription, translation, DNA methylation, histone modification, protein-nucleic acid interaction and much more.

The Facility operates the following technology platforms:

  • Illumina NovaSeq6000
  • Illumina NextSeq500
  • Illumina MiSeq
  • MinION (Oxford Nanopore)
  • Fluidigm C1 device for single-cell polyA+-RNA/DNA preparation
  • 10x Chromium Controller single-cell preparation.
  • RNA-Seq (full-length transcripts): sequencing of polyA+/rRNA-RNA for analysis of differentially expressed genes or transcriptome assembly
  • RNA-Seq (3'-ends): sequencing of 3'-ends of polyA+ RNA for analysis of differentially expressed genes or identification of transcription termination sites (TTS)
  • CAGE-Seq: sequencing of 5'-ends of polyA+ RNA for identification of transcription start sites (TSS)
  • SmallRNA-Seq: sequencing of small/micro RNAs for expression profiling
  • ISO-Seq: sequencing of polyA+RNA for transcriptome assembly/transcript isoform discovery
  • ChIP-Seq: sequencing of DNA following chromatin immunoprecipitation to identify protein binding sites
  • ATAC-Seq: genome-wide sequencing of transposase accessible DNA (open chromatin)
  • WES: whole exome sequencing for variant discovery
  • WGS: whole genome sequencing for variant discovery or genome assembly
  • Amplicon-Seq: amplicon sequencing for variant discovery or DNA methylation analysis
  • WGBS/RRBS: whole genome/reduced representation bisulfite sequencing for DNA methylation analysis (5mC and/or 5hmC)
  • scRNA-Seq: sequencing of 3' ends of polyA+ RNAs of single cells for analysis of differentially expressed genes
  • scATAC-Seq: genome-wide sequencing of transposase accessible DNA (open chromatin) in single-cell resolution
  • scMultiome: combined scRNA-Seq and scATAC-Seq in single-nuclei resolution

Internal users:
Download (excel) Sample registration form (SRF) for requesting NGS.

Download (excel) Quality check form (QCF) for requesting QC of RNA/DNA.

 

External users:
Please inquire.

Team (incomplete due to Data protection)

NameTelefonE-MailTätigkeit
Marco Groth+49 3641 656054marco.groth@leibniz-fli.deCore Facility Manager
Martin Bens+49 3641 656801martin.bens@leibniz-fli.dePostdoc
Ivonne Görlich+49 3641 656242ivonne.goerlich@leibniz-fli.deTechnischer Assistent
Cornelia Luge+49 3641 656242/6442cornelia.luge@leibniz-fli.deTechnischer Assistent
Christoph Englert+49 3641 656042christoph.englert@leibniz-fli.deWissenschaftlicher Betreuer

* unvollständig aufgrund DSGVO

For publications of individual CF members:  publications search 

Contact

Marco Groth
CF Manager
+49 3641 65-6054
marco.grothleibniz-flide

Overview CF DNA Sequencing