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<div class="plainlinks">'''Languages:''' [[Glossary|English]] | [[Glossary/zh|中文]] | [[Glossary/es|español]] | [[Glossary/fr|français]] | [[Glossary/de|Deutsch]] | [[Glossary/ja|日本語]]</div>
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= Glossary =
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= Glossaire =
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This glossary collects short definitions used across Nanopore Wiki.
Ce glossaire collecte des définitions courtes utilisées dans toute la Nanopore Wiki.
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; Basecalling
; Basecalling
: Conversion des données de signal nanopore en lectures de séquence nucléotidique.
: Converting nanopore signal data into nucleotide sequence reads.
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; Longue lecture
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: Une lecture de séquençage beaucoup plus longue que la sortie typique des lectures de séquençage à courte portée, souvent utile pour l'assemblage et la détection de variants structurels.
; Long read
: 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
: Un pore de nanométrique utilisé pour détecter les molécules par des changements de courant, de flux ionique ou d'autres signaux mesurables.
: A nanoscale pore used to sense molecules through changes in current, ion flow, or other measurable signals.
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; Read mapping
: Aligning sequencing reads to a reference genome or reference sequence.
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; Mappage de lecture
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: Alignement des lectures de séquençage sur un génome de référence ou une séquence de référence.
; Single-molecule sensing
: Detecting or measuring individual molecules rather than only bulk averages.
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; Détection de molécules uniques
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: Détection ou mesure de molécules individuelles plutôt que de moyennes en masse.
; Structural variant
: A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment.
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; Variant structurel
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: Un changement génomique tel qu'une insertion, une délétion, une duplication, une inversion ou une translocation qui affecte un segment de DNA plus important.

Revision as of 23:06, 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.