Our bioinformatics services include below analysis, deliverables and data management. AnalysisQC and bioinformatics analysis is done in Illuminas Genome Studio software.DeliverablesExcel file summarizing information about the experimental setup and methods (MIAME.xls)5 folder:DecodeData – files used during scanning.GenomeStudio – executable file (.bsc) for the created GenomStudio project.ImageData

https://www.ctg.lu.se/genomic-services/array/bioinformatics-and-deliverables - 2025-07-29

This service is only for future sequencing projects at CTG. Requesting a project at CTGTo initiate a project using our available services, please start a project in iLab. You can login using your LucatID (SWAMID) on the Lund University iLab webpage.  RNA RNA concentration RNA Concentration is measured by a fluorometric method, using the Qubit 4 or Qubit Flex instruments. Available Assays: Broad Ra

https://www.ctg.lu.se/services/quality-control - 2025-07-29

Service projects are registered and processed in iLab, an online project managing software for core facilities. It provides transparency of projects and quotes. It also includes a booking schedule for some equipment. What is iLab?iLab is our core facility's online platform for managing sequencing service orders. Through iLab, you can:Request project consultationsGet price quotesInitiate library pr

https://www.ctg.lu.se/how-start-project - 2025-07-29

CTG has a wide range of services which include laboratory analysis and bioinformatics pipelines. We also offer advice on how to design your research project to allow for reliable results. Genomics Single Cell Transcriptomics Spatial Sequencing Quality Control

https://www.ctg.lu.se/services - 2025-07-29

Special Offers for New Users! Trying Parse Evercode for the first time? Enjoy up to 45% off your first run:Mini: 45% off, WT: 18% off, Mega 96: 8% off, Mega 384: 5% off Since 2019, CTG has offered a broad range of single-cell applications, providing expert knowledge, accessibility, and personalized support. We continuously update our methods and instruments in collaboration with local researchers,

https://www.ctg.lu.se/services/single-cell - 2025-07-29

The Universal kits (formerly Next GEM Gene Expression) offer scalable whole transcriptome profiling at the single-cell level, with flexible sample input options. The 3' assay can be paired with cell surface protein staining, while the 5' assay supports full-length TCR/BCR sequencing, antigen specificity, CRISPR guide analysis, and cell surface protein profiling. For cost efficiency, samples can be

https://www.ctg.lu.se/services/single-cell/universal-3-or-5-gene-expression - 2025-07-29

Flex Gene Expression by 10x Genomics enables high-sensitivity single-cell profiling while preserving sample biology through fixation at collection. This approach stabilizes RNA, allowing flexible handling and batching without compromising data quality. As the most sensitive 10x Genomics application, it supports built-in sample multiplexing, processing up to 16 samples in a single GEM reaction. It

https://www.ctg.lu.se/services/single-cell/flex-gene-expression - 2025-07-29

The cost for a project varies according to the application and the number of samples. Please contact CTG for the specific pricing for your project. Pricing information can be found at your iLAB account. Contact InformationE-Mailctg_service [at] med [dot] lu [dot] sesinglecell [dot] ctgservice [at] med [dot] lu [dot] sePhone+46 73 075 3563+46 73 096 8048AddressBMC - Biomedical Centre D14Klinikgatan

https://www.ctg.lu.se/prices - 2025-07-29

Single-cell genomics now available for all users at Lund UniversitySince March 2019 CTG offers a dynamic, state-of-the-art platform for single-cell sequencing to users at Lund University. Here we will introduce the technologies available, the service provided, and how to start a project Introduction to the facilitySeptember 10, 2019 at 9.00 – 10:15Belfrage Lecture hall, BMC D15SpeakersMarkus Heide

https://www.ctg.lu.se/events - 2025-07-29

Contact InformationE-Mailctg_service [at] med [dot] lu [dot] sesinglecell [dot] ctgservice [at] med [dot] lu [dot] sePhone+46 73 075 3563+46 73 096 8048AddressBMC - Biomedical Centre D14Klinikgatan 32221 85 Lund

https://www.ctg.lu.se/publications/pre-prints - 2025-07-29

All customers using services at Center for Translational Genomics (CTG) should cite CTG by including the following sentence in the acknowledgments:"The authors would like to acknowledge Clinical Genomics Lund, SciLifeLab and Center for Translational Genomics (CTG), Lund University, for providing expertise and service with sequencing and analysis."  2025 The DNA methylation landscape of primary tri

https://www.ctg.lu.se/publications - 2025-07-29

CTG offers Sequencing-Only services for user-prepared libraries on the NovaSeq X Plus and NextSeq 2000 platforms. This service is designed for users who prepare their own sequencing-ready libraries and only require access to our Illumina instruments.What’s Included✔ Use of the selected Illumina sequencer✔ Required sequencing reagents✔ Instrument handling by CTG staff✔ Storage of data for 1 month a

https://www.ctg.lu.se/services/sequencing - 2025-07-29

Since 2019 CTG offers a dynamic, state-of-the-art platform for single-cell sequencing to users at Lund University with the aim to provide expertise, accessibility, proximity and service to researchers in need for single-cell genomics. General guidelines   Gentle sample isolation is essential not to bias against vulnerable cell types while fast isolation is desirable to reduce degradation of nuclei

https://www.ctg.lu.se/test-page-single-cell-genomics-platform - 2025-07-29

We offer comprehensive RNA sequencing services, including total RNA, mRNA, and small RNA library preparation and sequencing on Illumina platforms. Our services are tailored to meet the specific needs of each project, and we also provide consultation services for protocol development and collaborative research. Consultation Services:We offer consultations for project guidance and collaboration on p

https://www.ctg.lu.se/services/transcriptomics - 2025-07-29

https://www.clinicalgenetics.lu.se/department-clinical-genetics-0 - 2025-07-29

 The immune system has a remarkable capacity to scan tissues to recognize and eliminate abnormal and malignant cells. Scientific advances now allow us to improve and utilize this strength of the immune system against tumors.Our goal is to advance our ability to treat cancer using cell-based immunotherapy. By developing state-of-art genetic circuits and synthetic biology we strive to bring forward

https://www.clinicalgenetics.lu.se/axel-hyrenius-wittsten - 2025-07-29

https://www.clinicalgenetics.lu.se/startsidan - 2025-07-29

https://www.clinicalgenetics.lu.se/department-clinical-genetics-1 - 2025-07-29

Translating genomic discoveries into improved clinical decision making, mechanistic understanding, and therapy of acute leukemia The overall objective of our research is to significantly improve the way in which acute leukemia is diagnosed, understood at the functional/molecular level, and treated within health care.We work in three highly aligned and synergistic projects. In the first, new and cl

https://www.clinicalgenetics.lu.se/division-clinical-genetics/fioretos-research-group - 2025-07-29

  With a basis in stem cell biology, genetics, immunology and cancer research, our mission is to develop innovative immunotherapies that effectively target leukemia and other malignancies. To achieve this goal, we work on the following projects:•    Unravel immune evasion mechanisms in cancer. •    Development of therapeutic antibodies directed to novel targets.•    Development of CAR-macrophages

https://www.clinicalgenetics.lu.se/division-clinical-genetics/jaras-research-group - 2025-07-29