Resource Centre
726 results
Getting started guide: bulk transcriptomics
- Clinical research
- RNA
- cDNA
- Transcriptome
- Transcriptomics
- Fusion transcript
- Cancer research
- Human genomics
- Splice variation
- Isoforms
- Extraction
- Library prep
- PromethION
December 9 2024
Testimonial: Rapid detection of intra-amniotic infections in clinical research
- Clinical research
- Microbiology
- GridION
November 26 2024
Case study: full-length RNA isoforms deliver new insights into human health and disease
- Clinical research
- RNA
- mRNA
- Transcriptome
- Transcriptomics
- cDNA
- Neuroscience
- Human genomics
- PromethION
- Isoforms
November 6 2024
Case study: delivering ‘unique insights’ into infection with direct RNA sequencing
- Clinical research
- RNA
- mRNA
- Transcriptome
- Transcriptomics
- Isoforms
- Infectious disease
- Virus
- Methylation
- MinION
November 6 2024
Getting started guide: single-cell transcriptomics
- Clinical research
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
- Transcriptomics
- Cancer research
- Human genomics
- Variant calling
- Extraction
- Structural variation
- Bioinformatics
- EPI2ME
- Gene expression
- Gene fusions
- Immunology
- Isoforms
- Kits
- Library prep
- P2
- PromethION
- PromethION 2 Integrated
- Sample prep
- SNVs
November 1 2024
A rare case report of Prevotella lung abscess diagnosed using third-generation metagenomic sequencing
- Clinical research
- Microbiology
- MinION
September 26 2024
Implementing portable, real-time 16S rRNA sequencing in the healthcare sector enhances antimicrobial stewardship
- Clinical research
- Microbiology
- Infectious disease
- rRNA
September 25 2024
The potential of therapeutic mRNA — and how to measure it
- Clinical research
- Biopharma
- Cancer research
- MinION
- GridION
- Q-Line
- Targeted
September 18 2024
The art of GMP in the world of NGS: trials, tribulations, and a whole lot of acronyms — a success story
- Clinical research
- Biopharma
- Bioinformatics
- Human genomics
- GridION
- Structural variation
- Targeted
September 18 2024
Nanopore sequencing and functional screening of AAV genomes for optimal production and function
- Clinical research
- Biopharma
- Bioinformatics
- MinION
- Single cell
- Structural variation
September 18 2024
Antibody discovery through post-vaccination single-cell transcriptomics and haplotype-resolved germline sequencing
- Clinical research
- Biopharma
- Bioinformatics
- Human genomics
- Infectious disease
- P2
- PromethION
- EPI2ME
- Assembly
- Epigenetics
- Gene expression
- Single cell
- SNVs
- Phasing
- Structural variation
- Transcriptomics
- Whole genome
September 18 2024
Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
- Clinical research
- Bioinformatics
- Human genomics
- MinION
- Chromatin conformation
- Epigenetics
- Gene expression
- Targeted
- Whole genome
September 17 2024
Showcase: Carrier screening
- Clinical research
- Cancer research
- Bioinformatics
- Human genomics
- Population genomics
- MinION
- GridION
- EPI2ME
- GridION Q
- SNVs
- Phasing
- Structural variation
- Targeted
September 17 2024
Resolving structural configurations of DMD intragenic duplications through nanopore long-read sequencing
- Clinical research
- Bioinformatics
- Human genomics
- PromethION
- Structural variation
- Whole genome
September 17 2024
Nanopore sequencing in reproductive care
- Clinical research
- Human genomics
- Microbiology
- MinION
- GridION
- P2
- Structural variation
- Whole genome
September 17 2024
Nanopore-based random genomic sampling for intraoperative diagnosis of brain tumors and beyond
- Clinical research
- Cancer research
- Human genomics
- MinION
- P2
- Epigenetics
- Structural variation
- Whole genome
September 17 2024
Long-read sequencing for detecting methylation dysregulation
- Clinical research
- Bioinformatics
- Human genomics
- P2
- EPI2ME
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024
Long-read sequencing for comprehensive genomic profiling of infertile men
- Clinical research
- Bioinformatics
- Human genomics
- P2
- PromethION
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024
Long-read sequencing: bridging the diagnostic gap for undiagnosed cases in Chile
- Clinical research
- Bioinformatics
- Human genomics
- PromethION
- Targeted
- Whole genome
September 17 2024
DNA methylation signature detection using ultra-rapid, long-read nanopore genome sequencing
- Clinical research
- Bioinformatics
- Human genomics
- PromethION
- Epigenetics
- Whole genome
September 17 2024