125 years of BNITM

LinkedIn

Donation
r

Plain Language

Contact

Dr Dániel Cadar

Research Group Leader

phone: +49 40 285380-840

fax: +49 40 285380-400

email: cadar@bnitm.de

Next-Generation Sequencing Core Facility

 

The NGS Core Facility is an integrated unit of BNITM that provides NGS support and is now an integral part of the method scope for many research projects at BNITM and is used routinely. The unit operates several next-generation sequencers using Illumina synthesis sequencing technology, including NextSeq2000, NextSeq550, MiSeq and iSeq100, and maintains a fully equipped laboratory and qualified staff capable of performing a variety of sequencing applications from sample preparation to sequencing. The unit actively supports the planning and execution of these projects. We have established different workflows and pipelines for sample preparation to increase throughput and minimise technical variations. By centralising equipment and expertise, we have increased the efficiency and quality of the data generated. Library preparation for various applications is supported by a robust instrument infrastructure and closed laboratory system (e.g. Covaris, Bioanalyzer, Qubit, Pippin Prep, qPCR and more). The NGS unit offers various analyses in single or paired-end sequencing mode, including multiplexing libraries.

 

The Next-Generation Sequencing (NGS) unit of the BNITM can be seen. In the foreground is a large white box on a table. In the middle runs a wide luminous strip that glows pink-purple. At the top, you can see a large screen with the text estimated completion 18:26. In the background, there is more laboratory equipment on tables.
Next-Generation Sequencing (NGS) Unit of the BNITM   ©BNITM

The method portfolio includes standardised workflows and pipelines for various NGS applications:

  • Viral metagenomics and metatranscriptomics: RNA-Seq/DNA-Seq.
  • Complete transcriptome sequencing: Total RNA-Seq, mRNA
  • Insect genome sequencing
  • Exome sequencing
  • Discovery of small non-coding RNAs: ncRNA-Seq.
  • Genome-wide DNA methylation analysis: methyl/BS-Seq.
  • De novo sequencing and re-sequencing of genomic DNA.
  • Targeted enrichment and sequencing (Sequence Capture).
  • Single-cell genomic applications (scRNA-Seq, scDNA-Seq).
  • 16S metagenomic sequencing
  • miRNA and small RNA analysis
  • Long-range amplicon sequencing

 

 

A shot in a darkened room can be seen. A white device with a large monitor illuminates the darkness. The monitor is lit up in white, a circle is visible in which Tomorrow 14:14 is written. a small blue bar is also lit up on the device.
iSeq100 Sequencer   ©BNITM

Contact

  • Dr  Dániel Cadar
  • Laboratory Manager
  • phone: +49 40 285380-840
  • fax: +49 40 285380-400
  • email: cadar@bnitm.de