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Brochure: multiomic sequencing
- Human genomics
- Clinical research
- DNA
- gDNA
- cDNA
- RNA
- Direct analysis
- Transcriptome
- Epigenetics
- Methylation
- Whole genome
- Gene fusions
- Splice variation
- Isoforms
- Cancer research
- Single cell
March 13 2024
Detecting somatic mutations without matched normal samples using long reads
- Cancer research
- Human genomics
- Variant calling
- Structural variation
- SNVs
February 29 2024
Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes
- Cancer research
- PromethION
- Structural variation
- Methylation
- Phasing
- Epigenetics
February 23 2024
Powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
- Cancer research
- Transcriptome
- Isoforms
- Splice variation
- cDNA
- RNA
- Clinical research
- Human genomics
- Gene fusions
February 21 2024
Workflow: single-cell transcriptomics
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene fusions
- Gene expression
- Kits
February 20 2024
Nanopore-based consensus sequencing enables accurate multimodal tumour cell-free DNA profiling
- Cancer research
- cfDNA
- SNVs
February 17 2024
Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes
- Cancer research
- Targeted
- MinION
February 17 2024
Single-cell rapid capture hybridization sequencing (scRaCH-seq) to reliably detect isoform usage and coding mutations in targeted genes at a single-cell level
- Single cell
- Cancer research
- Transcriptome
- Isoforms
January 30 2024
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
- Cancer research
- Structural variation
- Targeted
January 23 2024
Ultra-rich nanopore data offers unprecedented insights into the transcriptomes of single cells
- Single cell
- RNA
- cDNA
- Human genomics
- Clinical research
- Transcriptome
- Cancer research
January 17 2024
Insights into the role of *JAK2*-I724T variant in myeloproliferative neoplasms from a unique cohort of New Zealand patients
- Cancer research
- Phasing
- Structural variation
January 10 2024
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
- Cancer research
- Single cell
- Transcriptome
January 2 2024
NCM 2023 Houston: Telomere dynamics in aging and cancer by nanopore long-read sequencing
- Cancer research
- Phasing
- Targeted
- GridION
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: Nanopore sequencing reveal structural heterogeneity in canine osteosarcoma
- Animal
- Bioinformatics
- Cancer research
- Phasing
- SNVs
- Structural variation
- Whole genome
- PromethION
- Q20+
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: Nanopore sequencing of cell-free DNA for methylation-based breast cancer detection
- Cancer research
- Whole genome
- PromethION
- Q20+
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: Haplotypes, isoforms, and fusions: towards a richer cancer transcriptome
- Bioinformatics
- Cancer research
- Human genomics
- Phasing
- SNVs
- Splice variation
- Transcriptome
- MinION
- PromethION
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: GoT-Splice: unraveling cell-type-specific impact of splicing factor mutations
- Bioinformatics
- Cancer research
- Human genomics
- Single cell
- Splice variation
- Transcriptome
- PromethION
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: Analysis of melanoma evolution using nanopore long-read sequencing data
- Bioinformatics
- Cancer research
- Epigenetics
- SNVs
- Structural variation
- PromethION
- Nanopore Community Meeting
December 6 2023
NCM 2023 Houston: AmplideX PCR and nanopore sequencing for accessible carrier screening for any lab
- Bioinformatics
- Cancer research
- Clinical research
- Human genomics
- SNVs
- Structural variation
- Targeted
- MinION
- GridION
- EPI2ME
- Nanopore Community Meeting
December 6 2023