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Integrated Exchange & Storage of Current and Future-Generation Immunogenomic Data

Integrated Exchange & Storage of Current and Future-Generation Immunogenomic Data
综合交易所
批准号:
9031118
负责人:
JILL Allison HOLLENBACH
金额:
$29.29万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-04-01 至 2019-02-28

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of the proposed work is to further develop and extend the functionality of our programs and protocols for the management and exchange of genetic data for the Human Leukocyte Antigen (HLA) and Killer cell Immunoglobulin-like Receptor (KIR) genes. These genes are central to immunity and critically important for human health, and constitute complex genetic systems with extraordinarily high levels of sequence and structural variation. Because these immunogenomic data have been generated using a wide variety of methods and under different nomenclature systems, cross-study data compatibility has remained an important and debilitating limitation to the field. The key element of the work proposed is the integration of the systems and standards that we have developed with existing public resources for the HLA and KIR gene systems to enable both reproducible and easily combined analyses of HLA and KIR data. To accomplish this, we will (1) expand and refine our Toolkit for Immunogenomic Data Exchange and Storage (TIDES) and Push Immunogenomics to the Next Generation (PING) software. We will improve TIDES by extending functionality for the KIR loci, expanding deployment options, expanding search and export capacity, refining the user interface, developing new algorithms for use with our novel Genotype List (GL) String data recording format, and better integrating TIDES with extant analytical software. We will automate our PING pipeline, extend its functionality to HLA class II loci, and integrate PING with TIDES; and (2) integrate PING, TIDES, and our GL Service with existing public registries, tools and databases. We will adapt PING to accept next generation sequencing (NGS) read data from the NCBI Sequence Read Archive (SRA) and Genotype and Phenotype Database (dbGaP), and to generate HLA and KIR genotypes using the NCBI MHC database (dbMHC) SBT Input tool. We will develop a LiftOver tool to manage GL Strings across multiple reference database releases. We will develop an HL7 messaging system that integrates GL Strings, GL Service Uniform Resource Identifiers (URIs) and Genetic Testing Registry (GTR) URIs, allowing the standard exchange of HLA and KIR typing results. We will partner with the NCBI to make these new services publically available, and will release all tools as free open source software. By facilitating ease of immunogenomic data management in this manner we will vastly increase the value of current and future data resources.
期刊论文(3)
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会议论文
DOI: 10.1007/s00251-014-0794-1
发表时间: 2014-11
期刊: IMMUNOGENETICS
影响因子: 3.2
作者: [Nemat-Gorgani, Neda, Edinur, Hisham A., Hollenbach, Jill A., Traherne, James A., Dunn, Paul P. J., Chambers, Geoffrey K., Parham, Peter, Norman, Paul J.]
通讯作者: Norman, Paul J.
DOI: 10.1016/j.jaut.2015.06.010
发表时间: 2015-11
期刊: Journal of autoimmunity
影响因子: 12.8
作者: [Hollenbach JA, Oksenberg JR]
通讯作者: Oksenberg JR
Role of Natural Killer Cell Diversity in Multiple Sclerosis Risk and Disease Course
Role of Natural Killer Cell Diversity in Multiple Sclerosis Risk and Disease Course
The landscape of HLA mediated variation in health and immunity
MHC Variation in Host Response to SARS-CoV2 and COVID-19 Outcomes
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