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関連する概念動画

Gene Duplication and Divergence02:37

Gene Duplication and Divergence

8.1K
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
8.1K
Genome Copying Errors02:46

Genome Copying Errors

5.2K
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
5.2K
Point and Frameshift Mutations01:30

Point and Frameshift Mutations

1.3K
Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
1.3K
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

7.1K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
7.1K
Sanger Sequencing01:57

Sanger Sequencing

776.0K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
776.0K
Genome Annotation and Assembly03:36

Genome Annotation and Assembly

21.2K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
21.2K

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関連する実験動画

Updated: Feb 28, 2026

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
09:10

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

Published on: May 22, 2018

10.1K

パンゲノムアラインメント圧縮のための適応型トレースポイント

Hasitha Kaushan, Santiago Marco-Sola, Erik Garrison

    bioRxiv : the preprint server for biology
    |February 27, 2026
    PubMed
    まとめ
    この要約は機械生成です。

    適応型トレースポイントは、データの複雑さに応じてインテリジェントにセグメント化することにより、ゲノム配列アラインメントに対して優れた圧縮を提供します。この方法は、従来の固定サイズエンコーディングと比較して、大規模なゲノム比較のストレージ効率を大幅に向上させます。

    キーワード:
    ゲノム配列アラインメント圧縮パンゲノムトレースポイントゲノムバイオインフォマティクス計算生物学

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    Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
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    Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites

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    Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
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    Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

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    関連する実験動画

    Last Updated: Feb 28, 2026

    A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
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    A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

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    Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
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    Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites

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    Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
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    Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

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