Robert Månsson Welinder

Head of Unit: National Genomics Infrastructure, KTH Royal Institute of Technology

Key Publications
Aging is associated with functional and molecular changes in distinct hematopoietic stem cell subsets
2023
Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma
2022
Bhlhe40 function in activated B and TFH cells restrains the GC reaction and prevents lymphomagenesis
Journal of Experimental Medicine, 2022
Absence of a common founder mutation in patients with cooccurring myelodysplastic syndrome and plasma cell disorder
Blood, 2021
High-throughput ChIPmentation: freely scalable, single day ChIPseq data generation from very low cell-numbers
BMC Genomics, 2019

Within the frame of my research team at the National Genomics Infrastructure (NGI), our overarching aim is to develop and establish sequencing based technologies that can serve the wider Swedish research community.

Our research interests spans the omics field and range from establishing automated high-throughput epigenetic assays and flexible low input RNAsequencing platforms to developing whole-genome sequencing approaches to tackle analysis of FACS sorted single cells as well as complex tumor genomes. We are also interested in the base sequencing technology platforms and utilizing these to provide novel capabilities and spatial multi-omics assays.

Last updated: 2025-01-09

Content Responsible: Hampus Pehrsson Ternström(hampus.persson@scilifelab.uu.se)

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