The National Genomics Infrastructure (NGI) at SciLifeLab invites you to participate in a webinar on the Spatial Transcriptomics 10X Visium technology. Spatially resolved transcriptomics, recently pronounced Method of the Year by Nature Methods, has undoubtedly changed the way we understand complex tissues. With the recent launch of the 10X Genomics Visium assay, we can now offer spatially […]
Welcome to a webinar on de novo sequencing and analysis, a service that the National Genomics Infrastructure (NGI) and National Bioinformatics Infrastructure Sweden (NBIS) offers to its users. De novo, which translates to “starting from the beginning”, refers to the process of sequencing a novel genome from an organism where no previous reference sequence is available. The de novo analysis strategy is divided into separate stages, starting with (i) sequencing, (ii) assembly, and finally (iii) […]
National Genomics Infrastructure has now increased capacity for methylation calling, direct RNA sequencing, sequencing of ultra-long fragments to resolve structural variation.
In recent years, long-read DNA sequencing has replaced short-read technologies as the gold standard solution for a wide range of genomics applications. In addition to producing high quality de novo genome assembly, long-read technologies can be used to study complex structural variation, full-length RNA isoforms, detection of epigenetic signals, and much more. The adaptation of long-read sequencing is sweeping […]
We are pleased to invite you to our Spatial Proteomics Seminar organized together with SNP&SEQ Technology Platform/National Genomics Infrastructure (NGI). We will take you beyond the use of flow cytometry and focal microscopy into the intriguing and dynamic world of the cell-surface proteome of single cells through next-generation sequencing. Following the seminar, we will serve […]
In recent years, long-read DNA sequencing has replaced short-read technologies as the gold standard solution for a wide range of genomics applications. In addition to producing high-quality de novo genome assembly, long-read technologies can be used to study complex structural variation, full-length RNA isoforms, detection of epigenetic signals, and much more. The adaptation of long-read sequencing is sweeping through […]
National workshop for PhD students, postdocs, researchers, and other employees within Swedish academia, introducing the analysis of next generation sequencing data. Responsible teachers: Malin Larsson, Martin Dahlö, Roy Francis Contact information: edu.intro-ngs@nbis.se Important dates Application opens: 13-Jan-2025 Application closes: 23-Feb-2025 Confirmation to accepted students: Week 9, 2025 Course fee This online training event is […]
The future of integrated biology is here! Illumina and SciLifeLab National Genomics Infrastructure - NGI are hosting two Multiomics Day events in September. Join us for an engaging seminar to explore how Next-Generation Sequencing (NGS) is pushing the boundaries of biological research. We'll dive into the latest applications, from NGS-based proteomics and epigenomics to single-cell […]
The future of integrated biology is here! Illumina and SciLifeLab National Genomics Infrastructure - NGI are hosting two Multiomics Day events in September. Join us for an engaging seminar to explore how Next-Generation Sequencing (NGS) is pushing the boundaries of biological research. We'll dive into the latest applications, from NGS-based proteomics and epigenomics to single-cell […]
Epigenomics is a cornerstone of modern genomics, providing crucial insights into gene regulation and cellular function. The study of epigenetic modifications, such as DNA methylation, histone modifications, and non-coding RNA expression, has revolutionized our understanding of gene activity across diverse biological systems. With advancements in sequencing technologies, researchers can now investigate these modifications at a […]