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相关概念视频

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Alternative RNA Splicing02:18

Alternative RNA Splicing

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Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
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RNA Splicing01:32

RNA Splicing

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Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
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Translation01:31

Translation

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Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
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Mutations01:39

Mutations

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Overview
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Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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影响人类语音调的序列变异.

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概括

科学家们在12,901名冰岛人中发现了与语音和母音声学的遗传联系. 在ABCC9基因中常见的变异影响了语音调,为人类言语的遗传学提供了见解.

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科学领域:

  • 遗传学 是一个遗传学.
  • 生物声学是一种生物声学.
  • 人类进化人类进化

背景情况:

  • 人类声系统和个体声音/语音变异的遗传基础在很大程度上仍未被探索.
  • 了解声音特征的遗传基础对于从语言学到医学等领域至关重要.

研究的目的:

  • 调查对声调和母音声学的遗传影响.
  • 识别与人类声音特征变异相关的特定遗传变异.
  • 探索声乐特征与其他生物和认知因素之间的相关性.

主要方法:

  • 分析了来自12,901名冰岛人的基因组测序数据.
  • 从语音录音中测量了语音和元音声学.
  • 进行统计分析以将遗传数据与声学测量和其他特征相关联.

主要成果:

  • 语音和母音声学表明一种遗传的组成部分.
  • 研究人员发现,ABCC9基因的常见变异与语音调有关.
  • 这些ABCC9变体还与上腺基因表达和心血管特征有关.

结论:

  • 语音声学,包括语音音和元音特征,受到遗传因素的影响.
  • 鉴定ABCC9变异提供了与语音音调的遗传联系.
  • 这项研究代表了向了解人类声系统的遗传基础和进化方面迈出的重要一步.