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= Glossary = | = Glossary = <!--T:1--> | ||
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This glossary collects short definitions used across Nanopore Wiki. | This glossary collects short definitions used across Nanopore Wiki. | ||
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; Basecalling | ; Basecalling | ||
: Converting nanopore signal data into nucleotide sequence reads. | : Converting nanopore signal data into nucleotide sequence reads. | ||
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; Long read | ; Long read | ||
: A sequencing read that is much longer than typical short-read sequencing output, often useful for assembly and structural variant detection. | : A sequencing read that is much longer than typical short-read sequencing output, often useful for assembly and structural variant detection. | ||
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; Nanopore | ; Nanopore | ||
: A nanoscale pore used to sense molecules through changes in current, ion flow, or other measurable signals. | : A nanoscale pore used to sense molecules through changes in current, ion flow, or other measurable signals. | ||
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; Read mapping | ; Read mapping | ||
: Aligning sequencing reads to a reference genome or reference sequence. | : Aligning sequencing reads to a reference genome or reference sequence. | ||
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; Single-molecule sensing | ; Single-molecule sensing | ||
: Detecting or measuring individual molecules rather than only bulk averages. | : Detecting or measuring individual molecules rather than only bulk averages. | ||
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; Structural variant | ; Structural variant | ||
: A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment. | : A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment. | ||
Revision as of 22:38, 28 June 2026
Glossary
This glossary collects short definitions used across Nanopore Wiki.
- Basecalling
- Converting nanopore signal data into nucleotide sequence reads.
- Long read
- A sequencing read that is much longer than typical short-read sequencing output, often useful for assembly and structural variant detection.
- Nanopore
- A nanoscale pore used to sense molecules through changes in current, ion flow, or other measurable signals.
- Read mapping
- Aligning sequencing reads to a reference genome or reference sequence.
- Single-molecule sensing
- Detecting or measuring individual molecules rather than only bulk averages.
- Structural variant
- A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment.