Rasmus Olofzon

ORCID: 0000-0001-8079-8718
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About
Contact & Profiles
Research Areas
  • Single-cell and spatial transcriptomics
  • Hematopoietic Stem Cell Transplantation
  • Cancer Genomics and Diagnostics
  • Mesenchymal stem cell research
  • T-cell and B-cell Immunology
  • Cell Image Analysis Techniques
  • Acute Lymphoblastic Leukemia research
  • Zebrafish Biomedical Research Applications
  • Pregnancy and preeclampsia studies
  • Mobile Learning in Education
  • Educational Games and Gamification
  • Prenatal Screening and Diagnostics
  • Cytokine Signaling Pathways and Interactions
  • Epigenetics and DNA Methylation
  • Immune Cell Function and Interaction
  • MicroRNA in disease regulation
  • Augmented Reality Applications
  • Acute Myeloid Leukemia Research

Lund University
2020-2024

Abstract A decline in hematopoietic stem cell (HSC) function is believed to underlie hematological shortcomings with age; however, a comprehensive molecular understanding of these changes currently lacking. Here we provide evidence that transcriptional signature reported several previous studies on HSC aging linked stress-induced gene expression rather than aging. Our findings have strong implications for the design and interpretation studies.

10.1038/s43587-023-00558-z article EN cc-by Nature Aging 2024-01-16

Abstract As the scale of single-cell genomics experiments grows into millions, computational requirements to process this data are beyond reach many. Herein we present Scarf, a modularly designed Python package that seamlessly interoperates with other toolkits and allows for memory-efficient analysis millions cells on laptop or low-cost devices like single-board computers. We demonstrate Scarf’s memory compute-time efficiency by applying it largest existing RNA-Seq ATAC-Seq datasets. Scarf...

10.1038/s41467-022-32097-3 article EN cc-by Nature Communications 2022-08-08

The scarcity of hematopoietic stem cells (HSCs) restricts their use in both clinical settings and experimental research. Here, we examined a recently developed method for expanding rigorously purified murine HSCs ex vivo. After 3 weeks culture, only 0.1% exhibited the input HSC phenotype, but these accounted almost all functional long-term activity. Input displayed varying potential vivo self-renewal, with alternative outcomes revealed by single-cell multimodal RNA ATAC sequencing profiling....

10.7554/elife.91826.3 article EN cc-by eLife 2024-03-06

Knowledge of human fetal blood development and how it differs from adult is highly relevant to our understanding congenital immune disorders childhood leukemia, which the latter can originate in utero. Blood formation occurs waves that overlap time space, adding heterogeneity, necessitates single-cell approaches. Here, a combined immunophenotypic transcriptional map first trimester primitive presented. Using CITE-seq (cellular indexing transcriptomes epitopes by sequencing), molecular...

10.1182/bloodadvances.2023009808 article EN cc-by-nc-nd Blood Advances 2023-06-28

The scarcity of hematopoietic stem cells (HSCs) restricts their use in both clinical settings and experimental research. Here, we examined a recently developed method for expanding rigorously purified murine HSCs ex vivo. After 3 weeks culture, only 0.1% exhibited the input HSC phenotype, but these accounted almost all functional long-term activity. Input displayed varying potential vivo self-renewal, with alternative outcomes revealed by single-cell multimodal RNA ATAC sequencing profiling....

10.7554/elife.91826 article EN cc-by eLife 2023-11-07

ABSTRACT Single-cell transcriptomics facilitates innovative approaches to define and identify cell types within tissues populations. An emerging interest in the cancer field is assess heterogeneity of transformed cells, including identification tumor-initiating cells based on similarities their normal counterparts. However, such mapping often confounded by large effects total gene expression programs introduced strong perturbations as an oncogenic event. Here, we present Nabo, a novel...

10.1101/2020.09.30.321216 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2020-10-02

The scarcity of hematopoietic stem cells (HSCs) restricts their use in both clinical settings and experimental research. Here, we examined a recently developed method for expanding rigorously purified murine HSCs ex vivo. After three weeks culture, only 0.1% exhibited the input HSC phenotype, but these accounted almost all functional long-term activity. Input displayed varying potential vivo self-renewal, with alternative outcomes revealed by single cell multimodal RNA- ATAC-seq profiling....

10.7554/elife.91826.2 preprint EN 2024-01-24

The scarcity of hematopoietic stem cells (HSCs) restricts their use in both clinical settings and experimental research. Here, we examined a recently developed method for expanding rigorously purified murine HSCs ex vivo. After three weeks culture, only 0.1% exhibited the input HSC phenotype, but these accounted almost all functional long-term activity. Input displayed varying potential vivo self-renewal, with alternative outcomes revealed by single cell multimodal RNA- ATAC-seq profiling....

10.7554/elife.91826.1 preprint EN 2023-11-07

ABSTRACT The increasing capacity to perform large-scale single-cell genomic experiments continues outpace the computational requirements efficiently handle growing datasets. Herein we present Scarf, a modularly designed Python package that seamlessly interoperates with other toolkits and allows for memory-efficient analysis of millions cells on laptop or low-cost devices like single board computers. We demonstrate Scarf’s memory compute-time efficiency by applying it largest existing RNA-Seq...

10.1101/2021.05.02.441899 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2021-05-03

ABSTRACT The scarcity of hematopoietic stem cells (HSCs) restricts their use in both clinical settings and experimental research. Here, we examined a recently developed method for expanding rigorously purified murine HSCs ex vivo. After three weeks culture, only 0.1% exhibited the input HSC phenotype, but these accounted almost all functional long-term activity. Input displayed varying potential vivo self-renewal, with alternative outcomes revealed by single cell multimodal RNA- ATAC-seq...

10.1101/2022.06.20.496822 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-06-20

ABSTRACT Knowledge of human fetal blood development and how it differs from adult is highly relevant for our understanding congenital immune disorders as well childhood leukemia, the latter known to originate in utero. Blood production during occurs waves that overlap time space adding heterogeneity, which necessitates single cell approaches. Here, a combined immunophenotypic transcriptional map first trimester primitive presented. Using CITE-seq (Cellular Indexing Transcriptomes Epitopes by...

10.1101/2021.12.29.474425 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-12-29
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