Jessica nordlund uppsala universitet
Part of npj Precision Oncology, Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies.
Jessica Nordlund, Medicin, UU
Researcher at Department of Medical Sciences, Molecular Precision Medicine. Part of Hepatology Research, p. Contributions of de novo variants to systemic lupus erythematosus. A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing. Riihimäki, Miia; Fegraeus, K. Jaderkvist; Nordlund, Jessica; Waern, Ida et al. Part of Clinical Epigenetics, Increased MYB alternative promoter usage is associated with relapse in acute lymphoblastic leukemia.
Refining risk prediction in pediatric acute lymphoblastic leukemia through DNA methylation profiling. Single nucleus transcriptomics data integration recapitulates the major cell types in human liver. Part of Genes and Immunity, p. Part of Frontiers in Oncology, Single-cell transcriptomics delineates the immune cell landscape in equine lower airways and reveals upregulation of FKBP5 in horses with asthma.
Part of European Journal of Human Genetics, p. Part of Life Science Alliance, BCP neoplasms: same or different? Jessica Nordlund Associate Professor (Docent) and Research Group Leader at Uppsala University | Managing Director, National Genomics Infrastructure at SciLIfeLab Uppsala | co-founder. Part of Genes, Chromosomes and Cancer, p. Part of Blood, p. Part of Frontiers in Molecular Biosciences, Part of Scientific Reports, Transcriptome sequencing of archived lymphoma specimens is feasible and clinically relevant using exome capture technology.
Long-read whole-genome analysis of human single cells. Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop report. Jessica Nordlund, was started in The MPM research group develops and applies novel molecular approaches to analyze the genomes, transcriptomes, epigenomes and proteomes of clinical samples. Welcome to the research group in Molecular Precision Medicine.
Part of Cancer Medicine, p. Our research is focused on genomics and epigenomics in human diseases. Dumanski, Jan P. Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.
37 Uppsala. Fegraeus, Kim; Rosengren, Maria K. Comparison of high-throughput single-cell RNA-seq methods for ex vivo drug screening.
Therese Nordlund Edvinsson
Part of Scientific Reports, p. Multi-modal single cell sequencing of B cells in primary Sjögren's Syndrome. An endothelial regulatory module links blood pressure regulation with elite athletic performance. Part of Nature Communications, Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia. Part of EBioMedicine, Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH.
Quartet DNA reference materials and datasets for comprehensively evaluating germline variant calling performance. By integrating multiple types of -omics data with machine learning, we aim to identify molecular biomarkers that distinguish a given patient from other patients with similar clinical presentations, improve the precision of molecular diagnoses, and identify novel treatment approaches.
Part of Genome Biology, Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia. Email: nd @ Mobile phone: +46 70 Visiting address: Room BMC Db BMC, D, Husargatan 3. Immune cells lacking Y chromosome show dysregulation of autosomal gene expression. Jessica Nordlund.