
Genomics
Janine Altmüller
Profil
We operate Illumina, Oxford Nanopore and PacBio platforms and offer standard as well as customized library preparation workflows to our users.
Single-cell multi-omics and spatial biology technologies are a major focus of our work. Our integrated FACS unit enables us to select and isolate cells on site. A broad range of state-of-the-art single-cell applications are available for downstream analyses.
We constantly implement novel techniques in collaborative research projects and are closely working with clinical researchers to translate these technologies into systems medicine. By providing a multi-omics view on the pathophysiology of patient or model system samples, we support clinical scientists to delineate the underlying mechanisms of diseases like cancer, cardiovascular events, or neurological disorders.
The facility comprises three teams: Next Generation Sequencing, Single-Cell Technologies and Data Management. Please inform yourself about our terms and conditions if you plan to make use of our services.
Next Generation Sequencing Team (Dr. Tatiana Borodina)
We operate an impressive line of sequencing platforms (Illumina, PacBio, Oxford Nanopore), pipetting robots and analytical equipment. The team has extensive experience implementing novel protocols, automating library preparation, and methodological development.
Available services and technologies include:
- Consultations on NGS-related questions;
- Support in the experimental design of NGS projects;
- QC for DNA and RNA samples and sequencing libraries;
- Library preparation from bulk material for diverse -Seq applications:
- RNA sequencing (e.g. mRNA-, totalRNA-, 3’mRNA-, miRNA-Seq),
- DNA sequencing (e.g. whole genome, whole exome, amplicon, cfDNA),
- Epigenome (ChIP-Seq, Methyl-Seq, direct RNA and DNA sequencing);
- Short-read sequencing on Illumina instruments: iSeq, MiSeq, MiniSeq, NextSeq 2000, NovaSeq 6000, NovaSeq X plus;
- Long-read sequencing on Pacific Biosciences Sequel II;
- Long-read sequencing on Oxford Nanopore MinION and PromethION platforms
Single-Cell Technologies Team (Dr. Thomas Conrad)
The Single-cell technologies team provides access to an exceptionally wide range of cutting-edge single-cell and spatial multiomics approaches. To facilitate easy access for a broad user community, we provide close support from experimental design to sample preparation and data processing. In addition to regular services, we offer individual user training to enable independent access to our advanced instruments. Single-cell technologies are rapidly evolving; we therefore continuously implement novel approaches in the context of collaborative research projects.
Available services and technologies include:
- Counseling on study design
- Counseling on sample preparation
- FACS
- Droplet-based approaches (10X Genomics; Dolomite)
- Plate-based assays (Smart-Seq2/3; G&T-Seq; scBS+T-Seq)
- Spatial transcriptomics (10X Genomics Visium + Xenium; Nanostring GeoMx + CosMx)
Data Management Team (Dr. Marten Jäger)
The process of collection and processing of genomic data is still lacking sufficient level of standardisation. To close that gap, the group strives to implement automated software solutions for genomic data processing and analysis enabling effective introduction of quality control measures safeguarding reproducibility.
Regarding data management issues please contact helpdesk-genomics@charite.de.
Please refrain from directly contacting individual members of the data management group to avoid lost inquiries.
Steering Committee
BIH
Christian Conrad
Stefanie Großwendt
Ute Scholl
MDC
Yo Lee
Ilaria Piazza
Nikolaus Rajewsky
Guests
Nils Blüthgen (Charité)
Anton Henssen (MDC/Charité)
Team
Bastian Salewsky
bastian.salewsky@bih-charite.de
+49 30 450 669 048
Charité lab
Nucleic acids isolation | NGS library preparation | Illumina sequencing
Carola Dietrich
MDC lab
Droplet- and plate-based single-cell genomics
Caroline Braeuning
caroline.braeuning@mdc-berlin.de
+49 30 9406-3043
MDC lab
FACS unit manager | Droplet-based single-cell genomics
Catrin Janetzki
catrin.janetzki@bih-charite.de
+49 30 450 569 048
Charité lab
NGS library preparation | Illumina sequencing
Claudia Quedenau
+49 30 9406-3048
MDC lab
Lab management (MDC lab) | PacBio and Oxford Nanopore sequencing coordination | NGS library preparation
Cornelia Schlee
cornelia.schlee@bih-charite.de
+49 30 450 669 048
Charité lab
NGS library preparation | Illumina sequencing
Cornelius Fischer
cornelius.fischer@mdc-berlin.de
+49 30 9406-1357
Data management | Bioinformatics
Elisabeth Kirst
+49 30 9406-2995
MDC lab
NGS library preparation | Illumina sequencing
Francesca Solinas
francesca.solinas@mdc-berlin.de
+49 30 9406-1320
MDC lab
Droplet- and plate-based single-cell genomics
Izabela Plumbom
+49 30 9406-1320
MDC lab
Droplet- and plate-based single-cell genomics | Spatial transcriptomics
Janine Altmüller
janine.altmueller@mdc-berlin.de
janine.altmueller@bih-charite.de
+49 30 9406-1434
Head of BIH/MDC Genomics Technology Platform
Jeannine Wilde
+49 30 9406-1321
MDC lab
Illumina sequencing coordination (MDC lab) | NGS library preparation
Kerim Secener
aliKerim.secener@mdc-berlin.de
+49 30 9406-1320
MDC lab
PhD student
Kirsten Richter
Invoicing | Administrative support | Documentation management | Event organisation
Lorena Derezanin
lorena.derezanin@bih-charite.de
+49 30 450 569 048
Data management | Bioinformatics
Madlen Sohn
+49 30 9406-3266
MDC lab
NGS library preparation | Illumina sequencing
Marko Vukovic
MDC lab
Student assistant
Marten Jäger
+49 30 450 569 048
Data management | Bioinformatics
Michaela Seeger-Zografakis
+49 30 9406-1324
MDC lab
FACS support | Droplet-based single-cell genomics
Sarah Vitcetz
+49 30 9406-3041
MDC lab
Droplet- and plate-based single-cell genomics | Spatial transcriptomics
Somesh Sai
+49 30 9406-1342
MDC lab
PhD student
Tatiana Borodina
tatiana.borodina@mdc-berlin.de
+49 30 9406-1341
Team leader Next Generation Sequencing
Thomas Conrad
+49 30 9406-1481
Team leader Single Cell Technologies
Ulrike Krüger
+49 30 450 643 507
Charité lab
Project coordination and Lab management (Charité lab) | NGS library preparation | Illumina sequencing
Ute Ungethüm
+49 30 450 676 272
Charité lab
Coordination of large-scale projects (Charité lab) | Automation of nucleid acid extraction and QC assays
Publications
Next Generation Sequencing
For consulting and assistance in planning of a sequencing experiment please contact us at seqteam@mdc-berlin.de or seqteam@bih-charite.de.
NGS Services Prices
Actual pricelist valid for MDC and Charité users is available upon request.
Large-scale projects require individual cost calculation - please contact seqteam@mdc-berlin.de or seqteam@bih-charite.de.
Ordering
Services are currently ordered per email to seqteam@mdc-berlin.de or to seqteam@bih-charite.de or to the members of the NGS team you are already in contact with.
Each service project has to be registered by filling the Project Registration Form and a relevant Sample Transfer Form – forms are sent out per email.
The specific number assigned by the NGS team to each project is used as a reference for further communication.
Turnaround time
Generally, the projects are processed in the order of samples (libraries) receipt.
Scheduling of sequencing libraries preparation for any platform depends on the current workload and equipment availability.
Illumina sequencing schedule depends on how fast the samples requiring the same sequencing mode are collected to fill up a flowcell. If your ready sequencing libraries occupy the whole flowcell, usually they can be sequenced within 1-2 weeks after the delivery.
Loading of ready libraries on PacBio and Oxford Nanopore PromethION is also usually possible within 1-2 weeks, depending on the sequencing queue.
Single-Cell Technologies
Eventually, single-cell multi-omics approaches provide a unique opportunity to discover exclusive characteristics of a diseased cell state.
Available assays include the detection of gene expression profiles, open chromatin regions, DNA sequence, cell surface epitopes, or T- and B- cell receptor sequences, and combinations thereof for thousands of single-cells in parallel.
In addition, spatial transcriptomic approaches allow us to assay individual cells in their spatial context, and reconstruct tissue architecture and its changes in response to environmental cues or in disease states.
Our integrated FACS unit enables us to perform initial quality control of single-cell preparations, and to select and isolate cell populations directly on site for droplet- or plate-based assays.
As all single-cell projects require individual organization and individual project planning and sample handling, please contact Dr. Thomas Conrad – Thomas.Conrad@mdc-berlin.de for further consultation.
Please contact Caroline Braeuning (Caroline.Braeuning@mdc-berlin.de) for access to FACS.