Resource Centre
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
- cfDNA
- Cancer research
- Neuroscience
- Methylation
Same-day, multiplexed, high-accuracy targeted liquid biopsy approach for low-tumor content treatment response monitoring
- cfDNA
- Bioinformatics
- Cancer research
- SNVs
- Targeted
- London Calling
Real-time analysis of the cancer genome and fragmentome from plasma and urine cell-free DNA using nanopore sequencing
- cfDNA
- Cancer research
- MinION
Rapid brain tumour classification from sparse epigenomic data
- cfDNA
- Cancer research
- Methylation
- PromethION 24/48
- Real-time
- MinION
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
- cfDNA
- Human genomics
- Clinical research
- Cancer research
- Oncology
- DNA
Nanopore sequencing from liquid biopsy: analysis of copy number variants from cell-free DNA of lung cancer patients
- cfDNA
- Cancer research
- Clinical research
Nanopore-based consensus sequencing enables accurate multimodal tumour cell-free DNA profiling
- cfDNA
- Cancer research
- SNVs
- MinION
- PromethION
Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases
- cfDNA
- Methylation
- Cancer research
Long-read sequencing reveals aberrant fragmentation patterns and origins of circulating DNA in cancer
- cfDNA
- Cancer research
- Whole genome
Glioblastoma, IDH-wildtype with primarily leptomeningeal localisation diagnosed by nanopore sequencing of cell-free DNA from cerebrospinal fluid
- cfDNA
- Cancer research
- Methylation
Comprehensive landscape and oncogenic role of extrachromosomal circular DNA in malignant biliary strictures
- cfDNA
- Cancer research
- Structural variation
- SNVs
- PromethION 24/48
Classification of brain tumors by nanopore sequencing of cell-free DNA from cerebrospinal fluid
- cfDNA
- Cancer research
- Clinical research
- MinION
Accurate detection of circulating tumor DNA using nanopore consensus sequencing
- cfDNA
- Clinical research
- Cancer research
- Oncology
- Human genomics
- DNA
A relative-independent haplotype derivation method applied for non-invasive prenatal testing for chromosomal rearrangements in a pregnant carrier
- cfDNA
- Human genomics
- PromethION 24/48
- Structural variation