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関連する概念動画

Incomplete Dominance01:43

Incomplete Dominance

25.4K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
25.4K
Next-generation Sequencing03:00

Next-generation Sequencing

92.6K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
92.6K
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

11.4K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
11.4K
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

6.1K
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...
6.1K
Pedigree Analysis01:35

Pedigree Analysis

85.1K
Overview
85.1K
RNA-seq03:21

RNA-seq

10.4K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.4K

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関連する実験動画

Updated: Sep 9, 2025

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

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牛の配列決定と遺伝子型決定に関する基礎資料

Troy N Rowan1,2

  • 1Department of Animal Science, University of Tennessee, Knoxville, TN, USA, 37996.

Journal of animal science
|September 1, 2025
PubMed
まとめ

SNP配列のようなゲノタイプ化技術は 牛肉産業の改善を加速します 低コストのシーケンシングとインプテーションは,発見とルーティンゲノタイプ化のためにより多くのゲノムデータを提供します.

科学分野:

  • 動物ゲノム学
  • 農業バイオテクノロジー
  • 人口遺伝学

背景:

  • 遺伝子型決定技術は 牛肉産業に革命を起こし ゲノム選択を可能にしました
  • シングル・ヌクレオチド・ポリモルフィズム (SNP) 配列は,ゲノム選択プログラムにおいて中心的な役割を果たしてきた.
  • 配列と割り算の進歩は,配列に費用対効果の高い代替案を提供します.

研究 の 目的:

  • 配列ベースのゲノタイプ化,ゲノム配列化,および控除による低パス配列化を見直す.
  • ゲノム発見とルーチンゲノタイプ化のための低カバーシーケンシングと推定の可能性を探求する.

主な方法:

  • 現在のゲノタイプ化技術の概要
  • 配列と割り算の方法論についての議論
  • 費用対効果と情報提供の分析

主要な成果:

  • 配列と割り算は 配列よりもはるかに多くのデータを 低コストで提供します
  • 控えめな範囲のシーケンシングと 割り算は有望なアプローチです
  • シーケンシングコストの低下は これらの高度な方法の実現可能性を高めています
キーワード:
GWAS について勘定する牛についてゲノム予測シーケンシング

さらに関連する動画

Infinium Assay for Large-scale SNP Genotyping Applications
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Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

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Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform
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Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform

Published on: January 30, 2017

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関連する実験動画

Last Updated: Sep 9, 2025

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

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Infinium Assay for Large-scale SNP Genotyping Applications
13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

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Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform
09:04

Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform

Published on: January 30, 2017

7.9K

結論:

  • 低範囲の配列と推定は 牛の集団におけるゲノム発見を促すことができます
  • これらの方法は,日常的な遺伝子型決定の標準となるでしょう.
  • 技術的進歩は家畜の遺伝的改善を加速させることを約束しています