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III-CXT: Collaborative Research: A High-Throughput Approach to the Assignment of Orthologous Genes Based on Genome Rearrangement

III-CXT: Collaborative Research: A High-Throughput Approach to the Assignment of Orthologous Genes Based on Genome Rearrangement
III-CXT:协作研究:基于基因组重排的直系同源基因分配的高通量方法
批准号:
0711129
负责人:
Tao Jiang
金额:
$26.0万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-15 至 2011-08-31

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中文摘要
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英文摘要
Orthologous genes, or orthologs, are genes in different speciesthat have evolved directly from a common ancestral gene.Genome-scale assignment of orthologs is a fundamental andchallenging problem in computational biology, and has a wide rangeof applications in comparative genomics and functional genomics.This project continues the development of the parsimony approachfor assigning orthologs between closely related genomes which essentially attempts to transform one genome into another by the smallest number of genome rearrangementevents including reversal, translocation, fusion, and fission, as well asgene duplication events. The project addresses three key algorithmicproblems including (i) signed reversal distance withduplicates, (ii) signed transposition distance with duplicates,and (iii) minimum common string partition. Efficient solutions to each ofthese problems are combined and incorporated into a software system for ortholog assignment, called MSOAR. The project encompasses genome-wide analysis of orthologous (and paralogous) relationships on the human and mouse genomes to valdiate the approach, and more importantly,to address several important evolutionary biological questions including the characterization of gains and losses of duplicated genes in the two genomes, the elucidation of gene movements in one genome with respect to the other genome, and the quantification of different mechanisms of gene duplication.Intellectual merit.The parsimony approach presents a novel method for performing genome-wideortholog assignment that takes into account both gene sequences and locations.The above algorithmic problems are new in the literature and their solutionslikely require the introduction of novel algorithm design and analysistechniques. The questions regarding gene duplication and quantification of the duplication mechanisms in model species are of fundamental importance in evolutionary biology.Broader impact.As ortholog assignment is a fundamental problem in comparative genomics andhas become a routine practice in almost all areas of genomics, MSOARwill find itself a wide range of applications in biology and genomics.Moreover, the research will provide the training opportunity for two computer science graduate students in the interdisciplinary field of computational biology.Information concerning this NSF project will be provided at the website:http://msoar.cs.ucr.edu/
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Extremal Problems on Graphs and Hypergraphs
  • 批准号:
    1855542
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $10.04万
  • 财政年份:
    2019
  • 负责人:
    Tao Jiang
  • 依托单位:
EAGER: Transcript-Based Differential Expression Analysis for Population Data Without Predefined Conditions
  • 批准号:
    1646333
  • 项目类别:
    Standard Grant
  • 资助金额:
    $20.0万
  • 财政年份:
    2016
  • 负责人:
    Tao Jiang
  • 依托单位:
Extremal problems for sparse hypergraphs and graphs
  • 批准号:
    1400249
  • 项目类别:
    Standard Grant
  • 资助金额:
    $13.32万
  • 财政年份:
    2014
  • 负责人:
    Tao Jiang
  • 依托单位:
Collaborative Research: ABI Innovation: Genome-Wide Inference of mRNA Isoforms and Abundance Estimation from Biased RNA-Seq Reads
  • 批准号:
    1262107
  • 项目类别:
    Standard Grant
  • 资助金额:
    $56.99万
  • 财政年份:
    2013
  • 负责人:
    Tao Jiang
  • 依托单位:
国内基金
海外基金
吩嗪类化合物CXT-A3对乳腺癌干细胞的抑制作用及机制研究
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    55万元
  • 批准年份:
    2021
  • 负责人:
    奚涛
  • 依托单位: