The completion of sequencing the human genome in 2001 marked a transition in biomedical research. However, the most transformative aspect was not the completion of the genome sequence itself, or the catalog of genes that it produced. Rather, it was the technologies that were spawned by the genome project, including DNA microarrays, proteomics, metabolomics, and more recently. Next Generation DNA sequencing methods and high-throughput epigenetics platforms, which have transformed our approach to fundamental questions in basic, translational, and clinical research. Rather than looking at a single gene at a time, these technologies have given us the ability to explore the epigenetic marks and gene expression patterns of all of the transcripts in the genome and the proteins they encode, to survey the spectrum of variation in populations, or to look at genome-wide patterns of epigenetic variation, and to use these to search for patterns that correlate with disease. With the maturation of these technologies, the challenge is no longer generating the data, but rather, effectively collecting, managing, analyzing, and interpreting it. The goal of the Systems Biology, Bioinformatics, and Biostatistics Core is to provide a collaborative structure in which experienced statisticians and bioinformatics scientists will work together to support the various PPG Projects to develop testable hypotheses about genes associated with COPD and their functional roles in COPD pathogenesis. Many of these statisticians and bioinformatics scientists in Core A are included as co-investigators in the Projects, and they will work closely with the highly talented clinical, laboratory, and population scientists in each Project within this proposed PPG. Core A will serve a dual role, providing support for the collection, management, analysis and interpretation of the SNP, gene expression, and methylation profiling data using """"""""conventional"""""""" methods in bioinformatics while applying new systems-biology-based methods for analysis and interpretation of the data. The rationale behind creating a separate core is to supplement the strong quantitative analytical teams working on each of the various projects with bioinformatics and systems-based modeling expertise and to work to integrate data across projects.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL105339-02
Application #
8381266
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
2
Fiscal Year
2012
Total Cost
$363,320
Indirect Cost
$130,002
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Hayden, Lystra P; Cho, Michael H; Raby, Benjamin A et al. (2018) Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study. Respir Res 19:209
Yun, Jeong H; Lamb, Andrew; Chase, Robert et al. (2018) Blood eosinophil count thresholds and exacerbations in patients with chronic obstructive pulmonary disease. J Allergy Clin Immunol 141:2037-2047.e10
Peng, Cheng; Cardenas, Andres; Rifas-Shiman, Sheryl L et al. (2018) Epigenome-wide association study of total serum immunoglobulin E in children: a life course approach. Clin Epigenetics 10:55
Morrow, Jarrett D; Cho, Michael H; Platig, John et al. (2018) Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease. Hum Genomics 12:1
Wang, Xiaoyun; Polverino, Francesca; Rojas-Quintero, Joselyn et al. (2018) A Disintegrin and A Metalloproteinase-9 (ADAM9): A Novel Proteinase Culprit with Multifarious Contributions to COPD. Am J Respir Crit Care Med :
Lopes-Ramos, Camila M; Kuijjer, Marieke L; Ogino, Shuji et al. (2018) Gene Regulatory Network Analysis Identifies Sex-Linked Differences in Colon Cancer Drug Metabolism. Cancer Res 78:5538-5547
Morrow, Jarrett D; Glass, Kimberly; Cho, Michael H et al. (2018) Human Lung DNA Methylation Quantitative Trait Loci Colocalize with Chronic Obstructive Pulmonary Disease Genome-Wide Association Loci. Am J Respir Crit Care Med 197:1275-1284
Hayden, Lystra P; Hardin, Megan E; Qiu, Weiliang et al. (2018) Asthma Is a Risk Factor for Respiratory Exacerbations Without Increased Rate of Lung Function Decline: Five-Year Follow-up in Adult Smokers From the COPDGene Study. Chest 153:368-377
Sharma, Amitabh; Kitsak, Maksim; Cho, Michael H et al. (2018) Integration of Molecular Interactome and Targeted Interaction Analysis to Identify a COPD Disease Network Module. Sci Rep 8:14439
Qiu, Weiliang; Guo, Feng; Glass, Kimberly et al. (2018) Differential connectivity of gene regulatory networks distinguishes corticosteroid response in asthma. J Allergy Clin Immunol 141:1250-1258

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