Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
基本信息
- 批准号:RGPIN-2017-06883
- 负责人:
- 金额:$ 3.06万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2019
- 资助国家:加拿大
- 起止时间:2019-01-01 至 2020-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
My research centers on the development of Computer Science methods to help solve problems in Biology and Medicine. While my research has application to many areas of medicine and genomics, the unifying thread through all of my work is the development of novel computational methods, firmly within the domain of Computer Science, to solve these problems. In the next five years I want to focus on the development of three computational approaches that can be combined for more accurate and rapid capture and analysis of medical data. In all of these cases the effort will be primarily on developing novel computational methodology and approaches, rather than deployment of existing technologies in the medical setting, and many of the methods developed will be generalizable outside of the medical setting.******Aim 1 of my grant will be on the development of mobile devices and HCI techniques for the capture of data from a patient visit. The core interaction between a patient and their doctor involved the doctor making observations, taking notes (on computer or paper), and finally writing (or dictating) a report. This report serves as the main record of the full interaction with the patient and myriad of signs and symptoms visually interrogated by the doctor (not all of which may be recorded in the notes, especially if not abnormal). We propose to develop a next generation of user interfaces, using wearable technology on the clinician (camera and microphone), combined with mobile devices (tablets), integrated into the clinical workflow, and capable of capturing the full visual and audio spectrum of the patient interaction. ******In Aim 2 of the grant we will work to develop ML methodology to identify concepts from the captured data audio, video, and text. We will utilize biomedical ontologies to help improve the accuracy of the methods, training models that utilize proximity in text and proximity in biomedical ontology space to help train classifiers. We will work on integrating this approach into existing speech-to-text tools to help improve audio processing, and apply these approaches to audio recording of patient exams to test their accuracy.******Finally, in Aim 3 of the proposal we will work on data visualization of recorded patient data, with the aim of providing the clinician with a easy-to-understand summary of patient symptoms over time, as well as to allow for quick comparison between a patient and others with similar disorders (for differential diagnosis) and same disorder (to understand disease variability and prognosis).
我的研究中心是计算机科学方法的发展,以帮助解决生物学和医学中的问题。虽然我的研究应用于医学和基因组学的许多领域,但贯穿我所有工作的统一主线是开发新的计算方法,牢牢地在计算机科学领域内,以解决这些问题。 在接下来的五年里,我希望专注于开发三种计算方法,这些方法可以结合起来,更准确,更快速地捕获和分析医疗数据。在所有这些情况下,努力将主要集中在开发新的计算方法和方法上,而不是在医疗环境中部署现有技术,并且开发的许多方法将在医疗环境之外推广。我资助的目标1将是开发移动的设备和HCI技术,用于从患者访问中捕获数据。病人和医生之间的核心互动包括医生进行观察,做笔记(在电脑或纸上),最后写(或口述)报告。该报告作为与患者的完整互动以及医生目视询问的无数体征和症状的主要记录(并非所有体征和症状都记录在笔记中,特别是如果不异常)。我们建议开发下一代用户界面,在临床医生身上使用可穿戴技术(摄像头和麦克风),结合移动的设备(平板电脑),集成到临床工作流程中,并能够捕获患者交互的完整视觉和音频频谱。** 在目标2中,我们将致力于开发ML方法,以从捕获的数据音频,视频和文本中识别概念。我们将利用生物医学本体来帮助提高方法的准确性,训练模型,利用文本中的接近度和生物医学本体空间中的接近度来帮助训练分类器。我们将致力于将这种方法集成到现有的语音到文本工具中,以帮助改进音频处理,并将这些方法应用于患者检查的音频记录,以测试其准确性。最后,在提案的目标3中,我们将致力于记录患者数据的数据可视化,旨在为临床医生提供易于理解的患者症状随时间推移的摘要,并允许患者与其他患有类似疾病(用于鉴别诊断)和相同疾病(了解疾病变异性和预后)的患者之间的快速比较。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Brudno, Michael其他文献
Identifying Clinical Terms in Medical Text Using Ontology-Guided Machine Learning
- DOI:
10.2196/12596 - 发表时间:
2019-04-01 - 期刊:
- 影响因子:3.2
- 作者:
Arbabi, Aryan;Adams, David R.;Brudno, Michael - 通讯作者:
Brudno, Michael
Genome variation discovery with high-throughput sequencing data
- DOI:
10.1093/bib/bbp058 - 发表时间:
2010-01-01 - 期刊:
- 影响因子:9.5
- 作者:
Dalca, Adrian V.;Brudno, Michael - 通讯作者:
Brudno, Michael
Multiple whole genome alignments and novel biomedical applications at the VISTA portal
- DOI:
10.1093/nar/gkm279 - 发表时间:
2007-07-01 - 期刊:
- 影响因子:14.9
- 作者:
Brudno, Michael;Poliakov, Alexander;Dubchak, Inna - 通讯作者:
Dubchak, Inna
The Matchmaker Exchange API: Automating Patient Matching Through the Exchange of Structured Phenotypic and Genotypic Profiles
- DOI:
10.1002/humu.22850 - 发表时间:
2015-10-01 - 期刊:
- 影响因子:3.9
- 作者:
Buske, Orion J.;Schiettecatte, Francois;Brudno, Michael - 通讯作者:
Brudno, Michael
SCARPA: scaffolding reads with practical algorithms
- DOI:
10.1093/bioinformatics/bts716 - 发表时间:
2013-02-15 - 期刊:
- 影响因子:5.8
- 作者:
Donmez, Nilgun;Brudno, Michael - 通讯作者:
Brudno, Michael
Brudno, Michael的其他文献
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{{ truncateString('Brudno, Michael', 18)}}的其他基金
Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
- 批准号:
RGPIN-2017-06883 - 财政年份:2022
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
- 批准号:
RGPIN-2017-06883 - 财政年份:2021
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
- 批准号:
RGPIN-2017-06883 - 财政年份:2020
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
- 批准号:
RGPIN-2017-06883 - 财政年份:2018
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
- 批准号:
RGPIN-2017-06883 - 财政年份:2017
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Understanding Functional and Medical Impact of Genetic Variation
了解遗传变异的功能和医学影响
- 批准号:
327669-2012 - 财政年份:2016
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Understanding Functional and Medical Impact of Genetic Variation
了解遗传变异的功能和医学影响
- 批准号:
327669-2012 - 财政年份:2015
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computerized patient phenotyping to connect canadian clinical genetics clinics
连接加拿大临床遗传学诊所的计算机化患者表型分析
- 批准号:
446597-2013 - 财政年份:2015
- 资助金额:
$ 3.06万 - 项目类别:
Collaborative Health Research Projects
Understanding Functional and Medical Impact of Genetic Variation
了解遗传变异的功能和医学影响
- 批准号:
327669-2012 - 财政年份:2014
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Computerized patient phenotyping to connect canadian clinical genetics clinics
连接加拿大临床遗传学诊所的计算机化患者表型分析
- 批准号:
446597-2013 - 财政年份:2014
- 资助金额:
$ 3.06万 - 项目类别:
Collaborative Health Research Projects
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Computational Methods for Capturing and Analyzing Personalized Genomic and Medical Data
捕获和分析个性化基因组和医学数据的计算方法
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捕获和分析个性化基因组和医学数据的计算方法
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