Resource Centre
893 results
Getting started guide: single-cell transcriptomics
- Bioinformatics
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
- Transcriptomics
- Cancer research
- Human genomics
- Clinical research
- Variant calling
- Extraction
- Structural variation
- EPI2ME
- Gene expression
- Gene fusions
- Immunology
- Isoforms
- Kits
- Library prep
- P2
- PromethION
- PromethION 2 Integrated
- Sample prep
- SNVs
November 1 2024
Parallel molecular data storage by printing epigenetic bits on DNA
- Bioinformatics
- MinION
- MinKNOW
- Guppy
October 23 2024
Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells
- Bioinformatics
- Single cell
- Phasing
- Variant calling
- PromethION
September 25 2024
Using nanopore sequencing for mRNA vaccine quality control: a journey from R&D to GMP
- Bioinformatics
- Biopharma
- GridION
- Transcriptomics
September 18 2024
The art of GMP in the world of NGS: trials, tribulations, and a whole lot of acronyms — a success story
- Bioinformatics
- Biopharma
- Clinical research
- Human genomics
- GridION
- Structural variation
- Targeted
September 18 2024
Precision cell engineering enabled through nanopore sequencing
- Bioinformatics
- Biopharma
- P2
- Assembly
- Epigenetics
- Gene expression
- Whole genome
September 18 2024
NESSI-Seq: novel cfDNA methylation assays for biomarker discovery and precision medicine
- Bioinformatics
- Biopharma
- Cancer research
- Human genomics
- PromethION
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Targeted
- Whole genome
September 18 2024
Nanopore sequencing and functional screening of AAV genomes for optimal production and function
- Bioinformatics
- Biopharma
- Clinical research
- MinION
- Single cell
- Structural variation
September 18 2024
Application of nanopore long-read sequencing to sterility testing for cell therapy products
- Bioinformatics
- Education
September 18 2024
Antibody discovery through post-vaccination single-cell transcriptomics and haplotype-resolved germline sequencing
- Bioinformatics
- Biopharma
- Clinical research
- Human genomics
- Infectious disease
- P2
- PromethION
- EPI2ME
- Assembly
- Epigenetics
- Gene expression
- Single cell
- SNVs
- Phasing
- Structural variation
- Transcriptomics
- Whole genome
September 18 2024
A sensitive sample preparation pipeline for adventitious virus detection using nanopore sequencing
- Bioinformatics
- Biopharma
- GridION
- Metagenomics
- Targeted
September 18 2024
Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach
- Bioinformatics
- Cancer research
- MinION
- Gene expression
- Transcriptomics
September 17 2024
Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
- Bioinformatics
- Clinical research
- Human genomics
- MinION
- Chromatin conformation
- Epigenetics
- Gene expression
- Targeted
- Whole genome
September 17 2024
Ultra-rich human data — variant analysis with EPI2ME
- Bioinformatics
- Human genomics
- Population genomics
- EPI2ME
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024
Showcase: Carrier screening
- Bioinformatics
- Cancer research
- Clinical research
- Human genomics
- Population genomics
- MinION
- GridION
- EPI2ME
- GridION Q
- SNVs
- Phasing
- Structural variation
- Targeted
September 17 2024
Secondary analysis update
- Bioinformatics
- EPI2ME
- Assembly
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024
Resolving structural configurations of DMD intragenic duplications through nanopore long-read sequencing
- Bioinformatics
- Clinical research
- Human genomics
- PromethION
- Structural variation
- Whole genome
September 17 2024
Positional mapping of active versus silenced rRNA gene clusters within A. thaliana nucleolus organizer regions
- Bioinformatics
- Plant
- GridION
- Assembly
- Chromatin conformation
- Epigenetics
- Gene expression
- Whole genome
September 17 2024
Obtaining reference genomes of emblematic and endangered Ecuadorian species
- Bioinformatics
- Animal
- Plant
- MinION
- P2
- Assembly
- Whole genome
September 17 2024
needLR: a structural variant filtering and prioritization tool for long-read sequencing data
- Bioinformatics
- Human genomics
- PromethION
- Assembly
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024