Genomes in Eye Disease: Methods to Query Variants Across Multiple Genome-wide Dat

眼病基因组：跨多个全基因组数据查询变异的方法

• 批准号: 8265100
• 负责人: THERESA GAASTERLAND
• 金额: $ 34.6万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-04-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8265100
• 关键词: Address; Affect; Age; Alleles; American; Biological Assay; Blindness; Code; Collaborations; Complex; Cost Savings; DNA; DNA Sequence; DNA Sequence Rearrangement; Data; Data Analyses; Data Set; Databases; Deposition; Derivation procedure; Disease; Disease Association; Early Diagnosis; Exons; Eye diseases; Funding; Genes; Genetic; Genome; Genotype; Glaucoma; Goals; Guidelines; Health Benefit; Heart; Human Genome; Individual; Institutes; Lead; Learning; Letters; Maps; Measures; Methods; National Heart, Lung, and Blood Institute; National Human Genome Research Institute; Pathogenesis; Patients; Phenotype; Prevention; Primary Open Angle Glaucoma; Proteins; Public Health; Quality Control; Reading; Research; Research Personnel; Risk; Secondary to; Series; Single Nucleotide Polymorphism; United States; United States National Institutes of Health; Universities; Variant; Visual impairment; Washington; Work; cohort; computerized tools; cost; data sharing; database of Genotypes and Phenotypes; design; disorder control; exome; gene discovery; genome sequencing; genome wide association study; genome-wide; improved; insertion/deletion mutation; insight; response; tool

DESCRIPTION (provided by applicant): Genomes in Eye Disease: Methods to Query Variants across Multiple Genome-wide Datasets. This application, in response to the NEI's RFA on Integrative Data Analysis, has two goals. Our first goal is to provide computational tools to support integrated gene-comparison queries that draw upon data from multiple, independent genome-wide DNA sequencing studies. Our second goal is to use these tools to discover genes associated with glaucoma by integrating over 300 exomes from glaucoma patients with 2500 exomes and genomes from other NIH-funded sequencing studies. Genome-wide assays for DNA substitutions, insertions, deletions, and rearrangements range in scope from measuring known single nucleotide polymorphisms (SNP), to sequencing al protein coding exons, to sequencing entire genomes. A number of NEI- and NIH-funded studies have generated distinct genome-wide datasets through studies of hundreds, or thousands, of patients. These studies generate both primary and secondary (derived) data. Primary data are the high quality, unmapped reads from patient DNA. Secondary data are the variants identified after mapping primary data to a reference human genome and calling substitutions, insertions, deletions, and rearrangements. Queries applied to the secondary data are limited in scope and accuracy by the methods used to generate the primary data and to derive the secondary data. Limitations on querying secondary data become more pronounced when multiple datasets are combined. To the extent that the original derivation methods differed, queries across multiple secondary datasets risk being incomplete or inaccurate and can return false answers. We will develop new tools that will address the limitations on querying secondary data, making it possible to compute accurate and meaningful answers to queries about gene-disease associations using multiple genome-wide DNA sequencing datasets. These tools will create a framework where each query drives re-derivation of variants from just the primary data necessary to answer the query accurately. We will use the tools to interrogate data relevant to the study of primary open angle glaucoma (POAG). These tools will be applied to four datasets relevant to glaucoma: exome sequence data from 300 POAG patients, bead-array genotype data from ~5,000 POAG patients, including the 300 exome subjects, and exome sequence data from two non-eye disease control cohorts, each with over 1,000 subjects. One control cohort will be from the NIH Intramural ClinSeq project; the other will be from an NHLBI funded heart study. The work will be accomplished in two aims. Aim 1 will build a coherent, quality-controlled reference dataset from the 2,800+ exomes. Aim 2 will build tools to compare an exome (or genome) dataset against the reference built in Aim 1 to discover and examine genes associated with POAG through rare variants. PUBLIC HEALTH RELEVANCE: This project seeks to develop tools that will make it possible to compute meaningful, correct, and accurate answers to queries about genes using multiple genome-wide datasets, with a focus on data relevant to the study of primary open angle glaucoma (POAG), the most common form of glaucoma in the United States and a leading cause of irreversible blindness and visual impairment worldwide, affecting more than 2.25 million Americans over age 40, and causing blindness in ~100,000 Americans and 3 million people worldwide each year. A number of NEI- and NIH-funded studies have already generated distinct datasets by applying these assays to hundreds or thousands of patients with and without eye-disease; an opportunity exists to use the different datasets together to learn more about genetic contributions to eye-disease. This research could have considerable public health benefit by identifying genes and their variants associated with pathogenesis of disease, leading to new strategies for early diagnosis, treatment and prevention.

描述（由申请人提供）：眼病基因组：跨多个全基因组数据集查询变异的方法。这个应用程序，作为对NEI关于综合数据分析的RFA的回应，有两个目标。我们的第一个目标是提供计算工具，以支持从多个独立的全基因组DNA测序研究中提取数据的综合基因比较查询。我们的第二个目标是利用这些工具，通过整合来自青光眼患者的300多个外显子组和来自其他nih资助的测序研究的2500个外显子组和基因组，来发现与青光眼相关的基因。DNA替换、插入、缺失和重排的全基因组测定范围从测量已知的单核苷酸多态性（SNP）到测序蛋白质编码外显子，再到测序整个基因组。许多由NEI和nih资助的研究通过对数百或数千名患者的研究产生了不同的全基因组数据集。这些研究产生了第一手和二手（衍生）数据。原始数据是来自患者DNA的高质量、未映射的读数。次要数据是将主要数据映射到参考人类基因组并调用替换、插入、删除和重排后确定的变体。应用于辅助数据的查询在范围和准确性上受到用于生成主要数据和派生辅助数据的方法的限制。当多个数据集组合在一起时，查询辅助数据的限制变得更加明显。由于原始的派生方法不同，跨多个辅助数据集的查询可能存在不完整或不准确的风险，并可能返回错误的答案。我们将开发新的工具来解决查询二级数据的限制，使使用多个全基因组DNA测序数据集计算关于基因-疾病关联的查询的准确和有意义的答案成为可能。这些工具将创建一个框架，其中每个查询驱动从准确回答查询所需的主要数据重新派生变体。我们将使用这些工具来询问与原发性开角型青光眼（POAG）研究相关的数据。这些工具将应用于与青光眼相关的四个数据集：来自300名POAG患者的外显子组序列数据，来自约5000名POAG患者的头阵列基因型数据，包括300名外显子组受试者，以及来自两个非眼病对照队列的外显子组序列数据，每个队列有1000多名受试者。一个对照队列将来自NIH校内ClinSeq项目；另一份来自NHLBI资助的心脏研究。这项工作将有两个目的。目标1将从2800多个外显子组中建立一个连贯的、质量可控的参考数据集。目标2将构建工具，将外显子组（或基因组）数据集与目标1中构建的参考数据进行比较，以通过罕见变异发现和检查与POAG相关的基因。