Revision as of 23:45, 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.

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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>
+<div lang="en" dir="ltr" class="mw-content-ltr">
+= Glossary =
+</div>
-= 术语表 =
+<div lang="en" dir="ltr" class="mw-content-ltr">
+This glossary collects short definitions used across Nanopore Wiki.
+</div>
-本术语表收集了在Nanopore Wiki中使用的简短定义。
+<div lang="en" dir="ltr" class="mw-content-ltr">
+; Basecalling
+: Converting nanopore signal data into nucleotide sequence reads.
+</div>
-; 基因测序
+<div lang="en" dir="ltr" class="mw-content-ltr">
-: 将纳米孔信号数据转换为核苷酸序列读数。
+; Long read
+: A sequencing read that is much longer than typical short-read sequencing output, often useful for assembly and structural variant detection.
+</div>
-; 长读长
+<div lang="en" dir="ltr" class="mw-content-ltr">
-: 比典型的短读长测序输出长得多的测序读数，通常用于组装和结构变异检测。
+; Nanopore
+: A nanoscale pore used to sense molecules through changes in current, ion flow, or other measurable signals.
+</div>
-; 纳米孔
+<div lang="en" dir="ltr" class="mw-content-ltr">
-: 用于通过电流、离子流或其他可测量信号的变化来感知分子的纳米级孔。
+; Read mapping
+: Aligning sequencing reads to a reference genome or reference sequence.
+</div>
-; 读长比对
+<div lang="en" dir="ltr" class="mw-content-ltr">
-: 将测序读数与参考基因组或参考序列对齐。
+; Single-molecule sensing
+: Detecting or measuring individual molecules rather than only bulk averages.
+</div>
-; 单分子检测
+<div lang="en" dir="ltr" class="mw-content-ltr">
-: 检测或测量单个分子，而不仅仅是整体平均值。
+; Structural variant
+: A genomic change such as an insertion, deletion, duplication, inversion, or translocation that affects a larger DNA segment.
+</div>
-; 结构变异
+<languages />
-: 影响较大DNA片段的基因组变化，如插入、删除、重复、倒位或易位。