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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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= Glossar =
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This glossary collects short definitions used across Nanopore Wiki.
Dieses Glossar sammelt kurze Definitionen, die im Nanopore-Wiki verwendet werden.
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; Basecalling
; Basecalling
: Die Umwandlung von Nanopore-Signaldaten in Nukleotidsequenzleseabschnitte.
: Converting nanopore signal data into nucleotide sequence reads.
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; Long read
; Long read
: Ein Sequenzleseabschnitt, der viel länger ist als typische kurze Sequenzleseabschnitte, oft nützlich für die Assembly und die Erkennung von strukturellen Varianten.
: 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
: Ein Pore im Nanometermaßstab, die zur Erfassung von Molekülen durch Änderungen des Stroms, des Ionenflusses oder anderer messbarer Signale verwendet wird.
: 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
: Das Anpassen von Sequenzleseabschnitten an ein Referenzgenom oder eine Referenzsequenz.
: Aligning sequencing reads to a reference genome or reference sequence.
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; Single-molecule sensing
; Single-molecule sensing
: Das Erkennen oder Messen einzelner Moleküle anstelle nur von Massendurchschnittswerten.
: Detecting or measuring individual molecules rather than only bulk averages.
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; Structural variant
; Structural variant
: Eine genomische Veränderung wie eine Einfügung, Löschung, Duplizierung, Inversion oder Translokation, die ein größeres DNSegment betrifft.
: A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment.
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Revision as of 22:39, 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.