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59 results

Adaptive sampling

Poster
Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing
March 9 2026
Publication
Flexible and rapid validation of structural variation using adaptive sampling
February 23 2026
Publication
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
January 30 2026
Publication
Genetic diagnosis of CYP21A2-related CAH: adaptive sampling long-read sequencing is an accurate and scalable solution
January 22 2026
Workflow
Workflow overview: Hereditary Cancer Panel
January 20 2026
Publication
Targeted sequencing and iterative assembly of near-complete genomes
November 24 2025
Webinar
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
November 11 2025
Publication
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
November 10 2025
Publication
Enriching for answers in rare diseases
October 24 2025
Publication
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
October 3 2025
Knowledge exchange
Adaptive sampling explained: the future of flexible target enrichment
September 23 2025
Getting started guide
Getting started guide: human genomics
September 17 2025
Application note
Application note: Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel
September 16 2025
Publication
DNA methylation influences human centromere positioning and function
September 4 2025
Brochure
Flyer: Hereditary Cancer Panel
September 3 2025
Workflow
Workflow overview: pharmacogenomics with adaptive sampling
August 5 2025
Publication
Adaptive sampling with Oxford Nanopore offers a simple way to improve the efficiency of plant metagenomic studies
August 5 2025
Publication
A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript
July 31 2025
Publication
Accurate detection of D4Z4 repeats, methylation and allele haplotype in facioscapulohumeral muscular dystrophy 1 using nanopore sequencing
July 30 2025
Publication
Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms
June 26 2025

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Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing

Flexible and rapid validation of structural variation using adaptive sampling

Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars

Genetic diagnosis of CYP21A2-related CAH: adaptive sampling long-read sequencing is an accurate and scalable solution

Workflow overview: Hereditary Cancer Panel

Targeted sequencing and iterative assembly of near-complete genomes

Transforming hereditary cancer sequencing with adaptive sampling target enrichment

Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles

Enriching for answers in rare diseases

Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling

Adaptive sampling explained: the future of flexible target enrichment

Getting started guide: human genomics

Application note: Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel

DNA methylation influences human centromere positioning and function

Flyer: Hereditary Cancer Panel

Workflow overview: pharmacogenomics with adaptive sampling

Adaptive sampling with Oxford Nanopore offers a simple way to improve the efficiency of plant metagenomic studies

A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript

Accurate detection of D4Z4 repeats, methylation and allele haplotype in facioscapulohumeral muscular dystrophy 1 using nanopore sequencing

Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms

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