Канал: Oxford Nanopore Technologies

Comprehensive characterisation of the mouse retina transcriptome using long-read RNA sequencing

Comprehensive characterisation of the mouse retina transcriptome using long-read RNA sequencing

ElysION: step-by-step demo

ElysION: step-by-step demo

A survey of RNA modifications across the human transcriptome by direct RNA nanopore sequencing

A survey of RNA modifications across the human transcriptome by direct RNA nanopore sequencing

Consolidation of a long-read sequencing platform in southern South America

Consolidation of a long-read sequencing platform in southern South America

Unlocking comprehensive genome for large-scale projects

Unlocking comprehensive genome for large-scale projects

Showcase Biosurveillance

Showcase Biosurveillance

PRECISE: Revealing new insights into population scale genomics in Singapore

PRECISE: Revealing new insights into population scale genomics in Singapore

Nanopore sequencing at the intersection between the clinic and biotech

Nanopore sequencing at the intersection between the clinic and biotech

Microbial identification in biopharma

Microbial identification in biopharma

Antibody discovery through single-cell transcriptomics and haplotype-resolved germline sequencing

Antibody discovery through single-cell transcriptomics and haplotype-resolved germline sequencing

Using nanopore sequencing for mRNA vaccine quality control a journey from R&D to GMP

Using nanopore sequencing for mRNA vaccine quality control a journey from R&D to GMP

Adventitious agent screening by long-read NGS

Adventitious agent screening by long-read NGS

The art of GMP in the world of NGS: trials, tribulations & a whole lot of acronyms — a success story

The art of GMP in the world of NGS: trials, tribulations & a whole lot of acronyms — a success story

The potential of therapeutic mRNA — and how to measure it

The potential of therapeutic mRNA — and how to measure it

QC made easy, a practical overview of nanopore QC tests for biomanufacturing

QC made easy, a practical overview of nanopore QC tests for biomanufacturing

Nanopore sequencing and functional screening of AAV genomes for optimal production and function

Nanopore sequencing and functional screening of AAV genomes for optimal production and function

NESSI-Seq novel cfDNA methylation assays for biomarker discovery and precision medicine

NESSI-Seq novel cfDNA methylation assays for biomarker discovery and precision medicine

Application of nanopore long-read sequencing to sterility testing for cell therapy products

Application of nanopore long-read sequencing to sterility testing for cell therapy products

A sensitive sample preparation pipeline for adventitious virus detection using nanopore sequencing

A sensitive sample preparation pipeline for adventitious virus detection using nanopore sequencing

Precision cell engineering enabled through nanopore sequencing

Precision cell engineering enabled through nanopore sequencing

Implementation of sequencing in a regulated environment

Implementation of sequencing in a regulated environment

Secondary analysis update

Secondary analysis update

Bacterial isolate and plasmid sequencing

Bacterial isolate and plasmid sequencing

Direct RNA basecaller update

Direct RNA basecaller update

Dorado latest developments and future directions

Dorado latest developments and future directions

How good is good enough

How good is good enough

Diverse structural variants cluster near breakage-fusion-bridge site in cancer genomes

Diverse structural variants cluster near breakage-fusion-bridge site in cancer genomes

Detection of hidden antibiotic resistance through real-time genomics

Detection of hidden antibiotic resistance through real-time genomics

Nanopore-based random genomic sampling for intraoperative diagnosis of brain tumors and beyond

Nanopore-based random genomic sampling for intraoperative diagnosis of brain tumors and beyond

Unraveling gene expression patterns in pediatric germ cell tumors a nanopore sequencing approach

Unraveling gene expression patterns in pediatric germ cell tumors a nanopore sequencing approach

Decoding the spliced HIV-1 transcriptome with accurate long-read RNA sequencing

Decoding the spliced HIV-1 transcriptome with accurate long-read RNA sequencing

Is the water safe to drink? The rapid test is the missing link

Is the water safe to drink? The rapid test is the missing link

Studying disease-causing polymorphic transposable element insertions using nanopore sequencing

Studying disease-causing polymorphic transposable element insertions using nanopore sequencing

Maximizing the power of genomic sequencing in pediatric rare disease

Maximizing the power of genomic sequencing in pediatric rare disease

Detection of mosaic and somatic structural variants with Sniffles2

Detection of mosaic and somatic structural variants with Sniffles2

Evaluating the quality of long-read phasing methods in clinically relevant genes

Evaluating the quality of long-read phasing methods in clinically relevant genes

needLR a structural variant filtering and prioritization tool for long-read sequencing data

needLR a structural variant filtering and prioritization tool for long-read sequencing data

Resolving structural configurations of DMD intragenic duplications through nanopore sequencing

Resolving structural configurations of DMD intragenic duplications through nanopore sequencing

Long-read sequencing reveals the molecular landscape of mitochondrial DNA 6mA methylation

Long-read sequencing reveals the molecular landscape of mitochondrial DNA 6mA methylation

Nanopore sequencing in reproductive care

Nanopore sequencing in reproductive care

Genetic regulation of nascent RNA maturation revealed by direct RNA sequencing

Genetic regulation of nascent RNA maturation revealed by direct RNA sequencing

Understanding the binding of transcription factors by base-pair-resolution chromatin accessibility

Understanding the binding of transcription factors by base-pair-resolution chromatin accessibility

Obtaining reference genomes of emblematic and endangered Ecuadorian species

Obtaining reference genomes of emblematic and endangered Ecuadorian species

Mapping of active versus silenced rRNA gene clusters within A. thaliana nucleolus organizer regions

Mapping of active versus silenced rRNA gene clusters within A. thaliana nucleolus organizer regions

DNA methylation patterns explain missing heritability in maize

DNA methylation patterns explain missing heritability in maize

Long-read sequencing for detecting methylation dysregulation

Long-read sequencing for detecting methylation dysregulation

Long-read sequencing bridging the diagnostic gap for undiagnosed cases in Chile

Long-read sequencing bridging the diagnostic gap for undiagnosed cases in Chile

Large-scale methylation studies using nanopore sequencing

Large-scale methylation studies using nanopore sequencing

Long-read sequencing for comprehensive genomic profiling of infertile men

Long-read sequencing for comprehensive genomic profiling of infertile men

Bulk & single-cell nanopore transcriptomics to identify alternative splicing in renal tubule cells

Bulk & single-cell nanopore transcriptomics to identify alternative splicing in renal tubule cells

Detection of germline alterations in homologous recombination repair genes by adaptive sampling

Detection of germline alterations in homologous recombination repair genes by adaptive sampling

Redefining cancer characterization and predisposition insights through nanopore sequencing

Redefining cancer characterization and predisposition insights through nanopore sequencing

Use of Oxford Nanopore sequencing to evaluate potential transmission of hospital infections

Use of Oxford Nanopore sequencing to evaluate potential transmission of hospital infections

Apps update: Update from the Oxford Nanopore Technologies Applications team

Apps update: Update from the Oxford Nanopore Technologies Applications team

DNA methylation signature detection using ultra-rapid, long-read nanopore genome sequencing

DNA methylation signature detection using ultra-rapid, long-read nanopore genome sequencing

Smarter genomics for streamlined answers — ElysION, sample-to-answer nanopore sequencing device

Smarter genomics for streamlined answers — ElysION, sample-to-answer nanopore sequencing device

Individual cells matter — single-cell data analysis with EPI2ME

Individual cells matter — single-cell data analysis with EPI2ME

Ultra-rich human data — variant analysis with EPI2ME

Ultra-rich human data — variant analysis with EPI2ME

Individual cells matter — single-cell answers through nanopore sequencing

Individual cells matter — single-cell answers through nanopore sequencing

Showcase: Carrier screening

Showcase: Carrier screening

Driving the next frontier in multiomics: Oxford Nanopore Technology Update from NCM 2024

Driving the next frontier in multiomics: Oxford Nanopore Technology Update from NCM 2024

Advancing RNA liquid biopsy via nanopore sequencing

Advancing RNA liquid biopsy via nanopore sequencing

Secuenciación nanopore para estudios de conservación y biodiversidad en Latino América

Secuenciación nanopore para estudios de conservación y biodiversidad en Latino América

Sequencing and analysis of nanopore-only microbial isolates with the NO-MISS workflow

Sequencing and analysis of nanopore-only microbial isolates with the NO-MISS workflow

Implementing fast, accessible viral surveillance with nanopore sequencing

Implementing fast, accessible viral surveillance with nanopore sequencing

Enhanced microbial profiling and metagenomics with nanopore sequencing

Enhanced microbial profiling and metagenomics with nanopore sequencing

NCM Boston — See what you've been missing

NCM Boston — See what you've been missing

NCM Boston — See what you've been missing

NCM Boston — See what you've been missing

How to load a PromethION Flow Cell

How to load a PromethION Flow Cell

Knowledge Exchange: How direct RNA nanopore sequencing can enhance your research

Knowledge Exchange: How direct RNA nanopore sequencing can enhance your research

Core webinar: Scalable human genomic characterisation with nanopore characterisation

Core webinar: Scalable human genomic characterisation with nanopore characterisation

Celebrating a decade of DNA discoveries: 10 years of the MinION in microbiology

Celebrating a decade of DNA discoveries: 10 years of the MinION in microbiology

Accelerating precision oncology research with nanopore sequencing

Accelerating precision oncology research with nanopore sequencing

Seq&Treat: targeted sequencing for drug-resistant TB detection and treatment

Seq&Treat: targeted sequencing for drug-resistant TB detection and treatment

Whole-genome sequencing in PulseNet foodborne molecular surveillance systems

Whole-genome sequencing in PulseNet foodborne molecular surveillance systems

Empowering comprehensive sequencing at scale

Empowering comprehensive sequencing at scale

Respiratory metagenomics in clinical service

Respiratory metagenomics in clinical service

10 years of nanopore sequencing applications

10 years of nanopore sequencing applications

Public health

Public health

Direct sequencing of cytosine modification states from nanopore long-read data

Direct sequencing of cytosine modification states from nanopore long-read data

So many mods in so little time 45 RNA modifications profiled by direct RNA-Seq

So many mods in so little time 45 RNA modifications profiled by direct RNA-Seq

Establishing a nanopore sequencing facility for acute care in New Zealand

Establishing a nanopore sequencing facility for acute care in New Zealand

Exploration of long-read sequencing in the resolution of newborn screening

Exploration of long-read sequencing in the resolution of newborn screening

Advancing RNA liquid biopsy technology via nanopore sequencing

Advancing RNA liquid biopsy technology via nanopore sequencing

From sample to insight exploring human genomics with PromethION end

From sample to insight exploring human genomics with PromethION end

HERRO: haplotype-aware error correction of ultra-long nanopore reads

HERRO: haplotype-aware error correction of ultra-long nanopore reads

Pathogen safety in biopharma: sequencing to come

Pathogen safety in biopharma: sequencing to come

Informing infectious disease interventions with genomics during big events

Informing infectious disease interventions with genomics during big events

Precision immunology in transplant: paving the way to operational tolerance

Precision immunology in transplant: paving the way to operational tolerance

Long-read sequencing for pathogenic and novel variation discovery in rare diseases

Long-read sequencing for pathogenic and novel variation discovery in rare diseases

Rapid nephrogenomics for thrombotic microangiopathies

Rapid nephrogenomics for thrombotic microangiopathies

iDTECT® Integration Site Analysis assay: a paradigm shift for the quality control of biologics i...

iDTECT® Integration Site Analysis assay: a paradigm shift for the quality control of biologics i...

How to get started with nanopore sequencing and plan your experiment

How to get started with nanopore sequencing and plan your experiment

How to select the right library prep workflow for your experiment

How to select the right library prep workflow for your experiment

How to extract high-quality DNA and RNA

How to extract high-quality DNA and RNA

How to run your sequencing device and get started with data analysis

How to run your sequencing device and get started with data analysis

How to analyse your data with EPI2ME

How to analyse your data with EPI2ME

How to sequence microbial isolates with the NO-MISS workflow

How to sequence microbial isolates with the NO-MISS workflow

Nanopore origins

Nanopore origins

Product demo: Integrated EPI2ME: streamlined analysis for clinical and biopharma

Product demo: Integrated EPI2ME: streamlined analysis for clinical and biopharma

Janessa Laskin: sequencing and the potential of personalised cancer treatment

Janessa Laskin: sequencing and the potential of personalised cancer treatment

Kathleen Zeglinski: direct RNA nanopore sequencing for gene therapy quality control

Kathleen Zeglinski: direct RNA nanopore sequencing for gene therapy quality control

Guillaume Cogan: uncovering new insights in Parkinson's

Guillaume Cogan: uncovering new insights in Parkinson's

Daniel Kim: cell-free RNA sequencing for early cancer characterisation

Daniel Kim: cell-free RNA sequencing for early cancer characterisation

In Situ Lab Initiative team: portable sequencing to tackle loss of biodiversity

In Situ Lab Initiative team: portable sequencing to tackle loss of biodiversity

Pedro Garrido-Rodriguez: direct RNA sequencing and epitranscriptomics

Pedro Garrido-Rodriguez: direct RNA sequencing and epitranscriptomics

Heather Ritchie-Parker: assembling reference genomes to inform conservation strategies

Heather Ritchie-Parker: assembling reference genomes to inform conservation strategies

Miten Jain: a decade of nanopore sequencing

Miten Jain: a decade of nanopore sequencing

Alexander Wittenberg: telomere-to-telomere banana genomes

Alexander Wittenberg: telomere-to-telomere banana genomes

Amanda Warr: understanding microbiomes, viruses and transmission

Amanda Warr: understanding microbiomes, viruses and transmission

Nick Loman: identifying potential viral threats

Nick Loman: identifying potential viral threats

Sarah Buddle: infectious disease research & EPI2ME for metagenomic data

Sarah Buddle: infectious disease research & EPI2ME for metagenomic data

Advancements in nanopore sequencing for enhanced food safety and quality assurance webinar

Advancements in nanopore sequencing for enhanced food safety and quality assurance webinar

Bringing nanopore sequencing into the clinical microbiology setting with targeted approaches

Bringing nanopore sequencing into the clinical microbiology setting with targeted approaches

Ultra-fast, deep-learned CNS tumour classification during surgery

Ultra-fast, deep-learned CNS tumour classification during surgery

Nanopore sequencing reveals conservation of chromosome end-specific telomere lengths

Nanopore sequencing reveals conservation of chromosome end-specific telomere lengths

Towards personalised medicine for breast cancer in the Caribbean: a pilot study

Towards personalised medicine for breast cancer in the Caribbean: a pilot study

Welcome back to London Calling 2024

Welcome back to London Calling 2024

Into the unknown: portable sequencing empowers global conservation genomics

Into the unknown: portable sequencing empowers global conservation genomics

Discovery of deeply intronic damaging mutations with nanopore sequencing

Discovery of deeply intronic damaging mutations with nanopore sequencing

Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog

Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog

CoRAL accurately resolves extrachromosomal DNA structures with long-read sequencing

CoRAL accurately resolves extrachromosomal DNA structures with long-read sequencing

Genomic studies of adeno-associated virus hepatitis

Genomic studies of adeno-associated virus hepatitis

100 years of Bordetella pertussis evolution in the UK

100 years of Bordetella pertussis evolution in the UK

Unlocking the banana pangenome: harnessing genetic diversity

Unlocking the banana pangenome: harnessing genetic diversity

Haplotype-resolved repeat expansions & methylation patterns in 1000 Genome Project data, Sophia ...

Haplotype-resolved repeat expansions & methylation patterns in 1000 Genome Project data, Sophia ...

BadgerSeq- a decentralized model for ultra-rapid, long-read whole-genome sequencing, Stephen Meyn

BadgerSeq- a decentralized model for ultra-rapid, long-read whole-genome sequencing, Stephen Meyn

Plant T2T genome assembly using ultra-long and adaptive nanopore sequencing

Plant T2T genome assembly using ultra-long and adaptive nanopore sequencing

LC24 Studio: Clinical and translational applications, technology improvements and future directions

LC24 Studio: Clinical and translational applications, technology improvements and future directions

LC24 Studio: Rapid tumour classification and the potential to transform patient care

LC24 Studio: Rapid tumour classification and the potential to transform patient care

LC24 Studio: Mutations in breast cancer, pharmacogenetics & tools for single-cell research

LC24 Studio: Mutations in breast cancer, pharmacogenetics & tools for single-cell research

Full-length transcript atlas of the developing human cortex, Rosemary Bamford

Full-length transcript atlas of the developing human cortex, Rosemary Bamford

LC24 Studio: Equity & accessibility in science, innovation & collaboration, & learning from failure

LC24 Studio: Equity & accessibility in science, innovation & collaboration, & learning from failure

LC24 Studio: Health inequalities, citizen science, pathogen surveillance, and public health

LC24 Studio: Health inequalities, citizen science, pathogen surveillance, and public health

LC24 Studio: Pathogen surveillance, community and collaboration, and future improvements

LC24 Studio: Pathogen surveillance, community and collaboration, and future improvements

LC24 Studio: Highlights from day 1, opportunities for early career scientists, & future applications

LC24 Studio: Highlights from day 1, opportunities for early career scientists, & future applications

Accessing the biosynthetic gene repertoire of medicinal plants, Ronja Friedhoff

Accessing the biosynthetic gene repertoire of medicinal plants, Ronja Friedhoff

Long-read sequencing to solve exome negative Parkinson's disease, Guillaume Cogan

Long-read sequencing to solve exome negative Parkinson's disease, Guillaume Cogan

Single-cell characterization of transcript isoforms with long-read RNA sequencing, Rui Chen

Single-cell characterization of transcript isoforms with long-read RNA sequencing, Rui Chen

LC24 Studio: Innovations in conservation, RNA in liquid biopsy, and ribosomes

LC24 Studio: Innovations in conservation, RNA in liquid biopsy, and ribosomes

Genetic and epigenetic profiling of FSHD by nanopore sequencing, Morghan Lucas

Genetic and epigenetic profiling of FSHD by nanopore sequencing, Morghan Lucas

DNA modifications in specific nuclei populations purified from human brain tissue, Darren Soanes

DNA modifications in specific nuclei populations purified from human brain tissue, Darren Soanes

Full-length RNA isoforms in human colorectal cancer at single-cell resolution, Ping Lu

Full-length RNA isoforms in human colorectal cancer at single-cell resolution, Ping Lu

Real-time genomic characterization of pediatric acute leukemia using adaptive sampling, Julie Geyer

Real-time genomic characterization of pediatric acute leukemia using adaptive sampling, Julie Geyer

Simultaneous methylation and fusion detection for pediatric tumor characterization, Mathilde Filser

Simultaneous methylation and fusion detection for pediatric tumor characterization, Mathilde Filser

Combined RNAseq and long-read sequencing for unsolved cases, Tjakko van Ham

Combined RNAseq and long-read sequencing for unsolved cases, Tjakko van Ham

LC24 Studio: Understanding structural variation, population genomics & healthcare, & CRISPR safety

LC24 Studio: Understanding structural variation, population genomics & healthcare, & CRISPR safety

Joint fragmentomic and methylation signatures of cfDNA for cancer detection, Billy Lau

Joint fragmentomic and methylation signatures of cfDNA for cancer detection, Billy Lau

Using Oxford Nanopore sequencing in grapevine breeding

Using Oxford Nanopore sequencing in grapevine breeding

Computational paradigm for scalable, ultra-fast, & cost-efficient nanopore sequencing

Computational paradigm for scalable, ultra-fast, & cost-efficient nanopore sequencing

Identifying m6A RNA modifications in neuroblastoma cell lines, Jade Forster

Identifying m6A RNA modifications in neuroblastoma cell lines, Jade Forster

Assembling a T2T cattle genome with Oxford Nanopore readscattle genome with Oxford Nanopore reads

Assembling a T2T cattle genome with Oxford Nanopore readscattle genome with Oxford Nanopore reads

Early detection of poliovirus outbreaks in the DRC from 2021–2022, Alex Shaw

Early detection of poliovirus outbreaks in the DRC from 2021–2022, Alex Shaw

A survey of human RNA modifications by direct RNA nanopore sequencing, Logan Mulroney

A survey of human RNA modifications by direct RNA nanopore sequencing, Logan Mulroney

Patterns in genomic methylation determined with long-read sequencing

Patterns in genomic methylation determined with long-read sequencing

Real-time genomic surveillance with nanopore sequencing, Rhys White

Real-time genomic surveillance with nanopore sequencing, Rhys White

Quality control of gene therapy vectors using nanopore direct RNA sequencing, Kathleen Zeglinski

Quality control of gene therapy vectors using nanopore direct RNA sequencing, Kathleen Zeglinski

New frontiers in pharmacogenomics

New frontiers in pharmacogenomics

Empowering scientists with data literacy skills in long-read genomic sequencing

Empowering scientists with data literacy skills in long-read genomic sequencing

Genome science in high-school classrooms: inflammation, glutamate, and methylation

Genome science in high-school classrooms: inflammation, glutamate, and methylation

Molecular epidemiology of Enterovirus A71 in Senegal between 2013–2021

Molecular epidemiology of Enterovirus A71 in Senegal between 2013–2021

Innovating and improving genome diagnostics using targeted long-read sequencing

Innovating and improving genome diagnostics using targeted long-read sequencing

Plant T2T genome assembly using ultra-long and adaptive nanopore sequencing

Plant T2T genome assembly using ultra-long and adaptive nanopore sequencing

Computational paradigm for scalable, ultra-fast, & cost-efficient nanopore sequencing

Computational paradigm for scalable, ultra-fast, & cost-efficient nanopore sequencing

Isopod: detecting differential isoform usage from long-read single-cell data

Isopod: detecting differential isoform usage from long-read single-cell data

Long-read transcriptomics shows synaptic adaptation to amyloid pathology in Alzheimer’s

Long-read transcriptomics shows synaptic adaptation to amyloid pathology in Alzheimer’s

Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog

Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog

Long-read CaptureSeq identifies novel RNA isoforms of psychiatric risk genes

Long-read CaptureSeq identifies novel RNA isoforms of psychiatric risk genes

Rapid analysis of drug resistant M. tuberculosis complex

Rapid analysis of drug resistant M. tuberculosis complex

DNA and RNA modification calling

DNA and RNA modification calling

Long-read sequencing as the future of clinical genetic testing

Long-read sequencing as the future of clinical genetic testing

Optimizing QC testing of mRNA vaccines and therapeutics

Optimizing QC testing of mRNA vaccines and therapeutics

Dorado update

Dorado update

EPI2ME everywhere

EPI2ME everywhere

Basecaller advancements

Basecaller advancements

Application and use of long-read sequencing in personalized cancer medicine

Application and use of long-read sequencing in personalized cancer medicine

De novo assembly of Oxford Nanopore reads

De novo assembly of Oxford Nanopore reads

Adaptive sampling reveals pathogenic repeat expansion in spinocerebellar ataxia

Adaptive sampling reveals pathogenic repeat expansion in spinocerebellar ataxia

Igniting single-cell analysis of full-length RNA isoforms in brain development

Igniting single-cell analysis of full-length RNA isoforms in brain development

Robbing the array to feed the pore: exploring ultra-fast brain tumour diagnosis

Robbing the array to feed the pore: exploring ultra-fast brain tumour diagnosis

An unprecedented metagenomic landscape of European and North American coastal samples

An unprecedented metagenomic landscape of European and North American coastal samples

Discovery of deeply intronic damaging mutations with nanopore sequencing

Discovery of deeply intronic damaging mutations with nanopore sequencing

Innovations in mRNA vaccine precision manufacturing

Innovations in mRNA vaccine precision manufacturing

EPI2ME democratising bioinformatics from point-and-click analysis to custom integrations

EPI2ME democratising bioinformatics from point-and-click analysis to custom integrations

Genomic sequencing for characterizing tumor minimal residual disease versus early cancer

Genomic sequencing for characterizing tumor minimal residual disease versus early cancer

Nanopore sequencing medically relevant dark genomic regions

Nanopore sequencing medically relevant dark genomic regions

ORG.one to 10

ORG.one to 10

Long-read sequencing reveals diverse patterns of epigenetic inheritance in mice

Long-read sequencing reveals diverse patterns of epigenetic inheritance in mice

What the cat dragged in emergence of a highly pathogenic feline canine recombinant coronavirus

What the cat dragged in emergence of a highly pathogenic feline canine recombinant coronavirus

Targeted sequencing of the entire blood group genome by adaptive sampling

Targeted sequencing of the entire blood group genome by adaptive sampling

Breaking boundaries in neurodegenerative disease research

Breaking boundaries in neurodegenerative disease research

Designing custom workflows with EPI2ME for real-time Salmonella detection

Designing custom workflows with EPI2ME for real-time Salmonella detection

An (epi-)genomics analysis of drug resistance in multiple myeloma

An (epi-)genomics analysis of drug resistance in multiple myeloma

Genomic surveillance of multidrug-resistant organisms based on long-read sequencing

Genomic surveillance of multidrug-resistant organisms based on long-read sequencing

Importance of adaptive sampling in nanopore long-read sequencing in pharmacogenetics

Importance of adaptive sampling in nanopore long-read sequencing in pharmacogenetics

LC24 Clinical and Biopharma Day Wrap

LC24 Clinical and Biopharma Day Wrap

London Calling 2024 highlights

London Calling 2024 highlights

rAAV genome sequencing uncovers transgene integrity and packaging impurities webinar

rAAV genome sequencing uncovers transgene integrity and packaging impurities webinar

London Calling 2024: Update from Clive Brown

London Calling 2024: Update from Clive Brown

MinION Mk1D: The next generation of portable sequencing

MinION Mk1D: The next generation of portable sequencing