在人类疾病中调查序列变异因果关系的指导方针
D G MacArthur1, T A Manolio2, D P Dimmock3
11] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts 02114, USA [2] Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts 02142, USA.
Nature
|April 25, 2014
概括
需要指导方针来准确识别引起疾病的遗传变异. 建立明确的标准将防止误诊,并改善我们对人类疾病的理解,加速基因组医学.
科学领域:
- 遗传学 是一个遗传学.
- 基因组医学是基因组医学.
- 生物信息学是一种生物信息学.
背景情况:
- 遗传变异的快速发现需要强大的临床解释方法.
- 区分致病变体和良性变体对于准确的疾病诊断至关重要.
- 目前缺乏标准化的指导方针,可能导致基因组数据的误解.
研究的目的:
- 解决对评估人类序列变异的明确指导方针的迫切需要.
- 提出一个框架来总结对变种病原性的信心.
- 在变体解释中识别挑战和资源需求.
主要方法:
- 审查目前在评估人类疾病的序列变异方面的挑战.
- 整合基因水平和变异水平的证据用于因果关系评估.
- 制定建议的信任总结指导方针.
主要成果:
- 确定了在区分致病源与功能变异方面面临的关键挑战.
- 提出了一个评估变种病原性信心的框架.
- 突出领域需要进一步开发变体解释资源.
结论:
- 标准化指导方针对于基因组数据的可靠临床应用至关重要.
- 准确的变体评估至关重要,以避免假阳性因果关系报告.
- 需要进一步开发资源,以支持变体解释和临床诊断.
相关概念视频
Criteria for Causality: Bradford Hill Criteria - II
1.7K
The Bradford Hill criteria serve as guidelines for establishing causative links in epidemiological research. Beyond Strength, Consistency, Specificity, and Temporality, key criteria also include Biological Gradient, Plausibility, Coherence, Experiment, and Analogy. These principles assist scientists in assessing the likelihood of causation in complex biological contexts. Below is a summary of these concepts:
1.7K
Genome-wide Association Studies-GWAS
12.6K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
12.6K
Criteria for Causality: Bradford Hill Criteria - I
1.7K
The Bradford Hill criteria are a group of principles that provide a framework to determine a causal relationship between a specific factor and a disease. There are nine criteria that are pivotal in assessing causality in epidemiological studies. Here's a closer look at Strength, Consistency, Specificity, and Temporality criteria with definitions and examples:
1.7K
Single Nucleotide Polymorphisms-SNPs
14.6K
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,...
14.6K
Causality in Epidemiology
2.2K
Causality or causation is a fundamental concept in epidemiology, vital for understanding the relationships between various factors and health outcomes. Despite its importance, there's no single, universally accepted definition of causality within the discipline. Drawing from a systematic review, causality in epidemiology encompasses several definitions, including production, necessary and sufficient, sufficient-component, counterfactual, and probabilistic models. Each has its strengths and...
2.2K
Comparing Copy Number Variations and SNPs
11.6K
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%...
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%...
11.6K


