Resource Centre
277 results
Workflow: tumour-normal sequencing
- SNVs
- Workflow
- Structural variation
- Epigenetics
- Methylation
- Cancer research
- Human genomics
- Whole genome
- PromethION
- Kits
- Sample prep
- Variant calling
August 4 2023
Workflow: large cohort sequencing
- SNVs
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
- Structural variation
- Variant calling
- Assembly
- Sample prep
- Library prep
- Methylation
October 12 2023
Workflow: human variant calling
- SNVs
- Human genomics
- Clinical research
- Cancer research
- PromethION
- Whole genome
- Variant calling
- Epigenetics
- Phasing
- Methylation
- Structural variation
July 5 2024
Whole-genome sequencing of SARS-CoV-2 in the Republic of Ireland during waves 1 and 2 of the pandemic
- SNVs
- MinION
- GridION
- Microbiology
- Outbreak
- cDNA
- RNA
- Amplicons
- Infectious disease
- Variant calling
February 10 2021
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
- SNVs
- Long-read
- Whole genome
- Human genomics
- Cancer research
- Oncology
- Structural variation
- Variant calling
- MinION
April 29 2021
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- SNVs
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
- Structural variation
- Methylation
May 15 2023
Whole genome sequencing and phylogenetic classification of Tunisian SARS-CoV-2 strains from patients of the Military Hospital in Tunis
- SNVs
- Microbiology
- Infectious disease
- Virus
- Outbreak
- GridION
- RNA
- cDNA
- Whole genome
- Clinical research
- Assembly
- Evolution
October 9 2020
Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
- SNVs
- Structural variation
- Whole genome
- London Calling
May 19 2023
Viral sequencing reveals US healthcare personnel rarely become infected with SARS-CoV-2 through patient contact
- SNVs
- GridION
- Microbiology
- Outbreak
- cDNA
- RNA
- Amplicons
- Infectious disease
- Variant calling
February 1 2021
Viral genetic sequencing identifies staff transmission of COVID-19 is important in a community hospital outbreak
- SNVs
- MinION
- Microbiology
- Outbreak
- cDNA
- RNA
- Amplicons
- Infectious disease
- Variant calling
February 19 2021
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci; addressing the need for deceased donor expedited HLA typing
- SNVs
- Human genomics
- Phasing
- DNA
- Amplicons
- Targeted
- MinION
- Clinical research
- Variant calling
- Flongle
June 25 2020
Using Targeted Nanopore Technologies
- SNVs
- DNA
- Targeted
- Phasing
- Structural variation
- Clinical research
January 27 2021
Using long-read nanopore sequencing to unravel structural genomic variations in plants
- SNVs
- London Calling
- Plant
- gDNA
- MinION
May 29 2019
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
- SNVs
- Phasing
- Long-read
- PromethION
- Methylation
- Chromatin conformation
May 15 2023
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
- SNVs
- Phasing
- Plant
- Structural variation
- Targeted
- London Calling
May 19 2023
Unique mutational changes in SARS-CoV2 genome of different state of India
- SNVs
- Microbiology
- Infectious disease
- Virus
- Outbreak
- RNA
- cDNA
- PromethION
- Whole genome
- Amplicons
- Assembly
- Variant calling
August 25 2020
Unique K-mer sequences for validating cancer-related substitution, insertion and deletion mutations
- SNVs
- Whole genome
- Variant calling
- gDNA
- DNA
- Bioinformatics
June 20 2020
Ultra-rich human data — variant analysis with EPI2ME
- SNVs
- Bioinformatics
- Human genomics
- Population genomics
- EPI2ME
- Epigenetics
- Phasing
- Structural variation
- Whole genome
September 17 2024
Ultra-rapid nanopore whole genome genetic diagnosis of dilated cardiomyopathy in an adolescent with cardiogenic shock
- SNVs
- Long-read
- Variant calling
- gDNA
- DNA
- PromethION
- Human genomics
- Clinical research
February 8 2022
Two cases of vancomycin-resistant Enterococcus faecium bacteremia with development of daptomycin-resistant phenotype and its detection using Oxford Nanopore sequencing
- SNVs
- Microbiology
- Bacteria
- AMR
- Clinical research
- Variant calling
- Whole genome
- MinION
- gDNA
- DNA
May 23 2020