Oxford Nanopore: Difference between revisions
Appearance
Marked this version for translation |
Expand Nanopore Wiki source page with structured educational content |
||
| Line 1: | Line 1: | ||
__NOTOC__ | |||
<translate> | <translate> | ||
<!--T:1--> | |||
[[File:Nanopore_sequencing_principle.png|thumb|right|320px|Nanopore sequencing principle. Openly licensed schematic used as a general visual guide.]] | |||
'''Oxford Nanopore''' is part of the Nanopore Wiki learning path. Oxford Nanopore Technologies develops nanopore sequencing instruments, flow cells, chemistry, and software for real-time DNA and RNA sequencing. | |||
<!--T:2--> | <!--T:2--> | ||
== Core concepts == | |||
* The platform reads electrical signals produced as molecules pass through nanopores. | |||
* Device families include portable and higher-throughput instruments. | |||
* Output can include raw signal files, basecalled reads, alignments, and analysis reports. | |||
* Performance depends on chemistry, flow cell quality, library preparation, basecaller model, and analysis settings. | |||
<!--T:3--> | |||
== Typical sequencing workflow == | |||
{| class="wikitable np-knowledge-table" | |||
! Step | |||
! Description | |||
|- | |||
| 1 | |||
| Prepare DNA or RNA library according to the assay. | |||
|- | |||
| 2 | |||
| Load library onto a flow cell and start sequencing. | |||
|- | |||
| 3 | |||
| Basecall raw signal into sequence reads and quality scores. | |||
|- | |||
| 4 | |||
| Run quality control, alignment, assembly, variant calling, modification calling, or classification. | |||
|} | |||
<!--T:4--> | <!--T:4--> | ||
== Typical applications == | |||
* Long-read genome sequencing. | |||
* Metagenomics and pathogen surveillance. | |||
* Transcriptomics and direct RNA sequencing. | |||
* Structural variant and modification detection. | |||
<!--T:5--> | |||
== Common pitfalls == | |||
* Comparing results without chemistry and model versions. | |||
* Ignoring read quality, pore count, run yield, and sample degradation. | |||
* Presenting research use as clinical guidance without validation. | |||
<!--T:6--> | <!--T:6--> | ||
== Related pages == | |||
* [[MinION]] | |||
* [[Nanopore sequencing]] | * [[Nanopore sequencing]] | ||
* [[Bioinformatics]] | * [[Bioinformatics]] | ||
* [[Platforms]] | |||
<!--T:7--> | |||
== References == | |||
* [https://en.wikipedia.org/wiki/Oxford_Nanopore_Technologies Oxford Nanopore Technologies] | |||
* [https://nanoporetech.com/ Oxford Nanopore Technologies] | * [https://nanoporetech.com/ Oxford Nanopore Technologies official site] | ||
</translate> | </translate> | ||
<languages /> | <languages /> | ||
Revision as of 10:12, 30 June 2026

Oxford Nanopore is part of the Nanopore Wiki learning path. Oxford Nanopore Technologies develops nanopore sequencing instruments, flow cells, chemistry, and software for real-time DNA and RNA sequencing.
Core concepts
- The platform reads electrical signals produced as molecules pass through nanopores.
- Device families include portable and higher-throughput instruments.
- Output can include raw signal files, basecalled reads, alignments, and analysis reports.
- Performance depends on chemistry, flow cell quality, library preparation, basecaller model, and analysis settings.
Typical sequencing workflow
| Step | Description |
|---|---|
| 1 | Prepare DNA or RNA library according to the assay. |
| 2 | Load library onto a flow cell and start sequencing. |
| 3 | Basecall raw signal into sequence reads and quality scores. |
| 4 | Run quality control, alignment, assembly, variant calling, modification calling, or classification. |
Typical applications
- Long-read genome sequencing.
- Metagenomics and pathogen surveillance.
- Transcriptomics and direct RNA sequencing.
- Structural variant and modification detection.
Common pitfalls
- Comparing results without chemistry and model versions.
- Ignoring read quality, pore count, run yield, and sample degradation.
- Presenting research use as clinical guidance without validation.