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84,503 grants matching bioinformatics

Bioinformatics

$874,518
Nicholas D Socci · Sloan-Kettering Inst Can Research · P30 · FY2024 · CA

Core C1: Data Interpretation Core

$874,506
Ronald Gary Tompkins · Massachusetts General Hospital · U54 · FY2010 · GM

Multiplexed Diagnostic and Cytokine Response Assays Utilizing the nCounter Platfo

$874,477
Pejman Naraghi-Arani · University Of Calif-Lawrnc Lvrmr Nat Lab · R01 · FY2012 · AI

Using Integrative Genomics To Identify and Characterize Emphysema-Associated eQTL

$874,473
Peter Castaldi · Brigham And Women'S Hospital · R01 · FY2017 · HL

MIM: Elucidating the Rules of Cooperation and Resiliency in Microbial Communities through Stochastic Graph Grammars

$874,451
Devaki Bhaya · Carnegie Institution Of Washington · · FY2021 · BIO

Development of a Genotoxicity Assay using Duplex Sequencing

$874,368
Jesse J Salk · Twinstrand Biosciences, Inc. · R44 · FY2020 · ES

Generation of Hematopoietic Stem and Progenitor Cells from Human iPSCs

$874,298
Andre Larochelle · National Heart, Lung, And Blood Institute · ZIA · FY2021 · HL

Human Variants

$874,239
Joann B Sweasy · University Of Vermont & St Agric College · P01 · FY2014 · CA

PRO: A Protein Ontology in OBO Foundry for Integration of Biomedical Knowledge

$874,165
Cathy H Wu · University Of Delaware · R01 · FY2014 · GM

Laboratory of Genetic Susceptibility

$874,077
Stephen J Chanock · Division Of Cancer Epidemiology And Genetics · ZIA · FY2018 · CA

Elucidation of cancer pathways and druggable targets using mouse models.

$873,915
Cory Abate-Shen · Columbia University Health Sciences · U01 · FY2011 · CA

CHOP Pediatric Center of Excellence in Nephrology

$873,905
Michelle Denburg · Children'S Hosp Of Philadelphia · P50 · FY2024 · DK

Biomedical Informatics Research Training at Yale

$873,873
Perry L Miller · Yale University · T15 · FY2010 · LM

Papillomavirus-like Particles (VLP) as Broad Spectrum Human Papillomavirus (HPV) Vaccines

$873,677
Joshua Weiyuan Wang · Pathovax, Llc · R44 · FY2019 · AI

Papillomavirus-like Particles (VLP) as Broad Spectrum Human Papillomavirus (HPV) Vaccines

$873,677
Joshua Weiyuan Wang · Pathovax, Llc · R44 · FY2020 · AI

Structural Genetic Variation in Asthma

$873,548
Benjamin Alexander Raby · Brigham And Women'S Hospital · R01 · FY2008 · HL

Clinical and Translational Science Award

$873,504
Robert Stanley Sherwin · Yale University · KL2 · FY2007 · RR

NIGMS National and Regional Resources - DNASU

$873,502
Joshua Labaer · Arizona State University-Tempe Campus · R24 · FY2023 · GM

NIGMS National and Regional Resources - DNASU

$873,502
Joshua Labaer · Arizona State University-Tempe Campus · R24 · FY2024 · GM

Develomental Core

$873,448
Sarah M Fortune · Harvard University · P30 · FY2017 · AI

Shared Genome Database Informatics and Cyber Infrastructure

$873,414
Donald G Gilbert · Indiana University · · FY2007 · BIO

High-Throughput Molecular Profiling Core

$873,345
Martin Thomas Ferris · Univ Of North Carolina Chapel Hill · U19 · FY2015 · AI

THIS PROJECT INVESTIGATES COFACTOR RNA CONJUGATES TO SHED LIGHT ON THE ORIGIN EARLY EVOLUTION AND EVOLUTIONARY HISTORY OF LIFE. THE BIOLOGY AND BIOCHEMISTRY OF THIS NEW CLASS OF RNAS RECENTLY OBSERVED IN BACTERIAL RNA FRACTIONS WILL EXPAND OUR UNDERSTANDING OF HOW NUCLEIC ACIDS AND THE SMALL MOLECULE METABOLOME WORK TOGETHER HOW THEY MAY SHAPE METABOLIC FLUX IN MODERN ORGANISMS ANDHOW THEY MAY HAVE CONTRIBUTED TO CATALYTIC DIVERSITY IN ANCIENT RNA ENZYMES. THE TWO AIMS BUILD UPON STRONG LITERATURE PRECEDENT AND PRELIMINARY DATA COMBINING INNOVATIVE EXPERIMENTAL AND BIOINFORMATICS APPROACHES IN AN INTEGRATED EXAMINATION OF A NOVEL CLASS OF RNA TRANSCRIPTS.AIM 1 BACTERIAL COA RNA CONJUGATES. RNA TRANSCRIPTS THAT CARRY COVALENTLY ATTACHED COENZYME A COA HAVE BEEN UNAMBIGUOUSLY DEMONSTRATED TO EXIST IN E. COLI AND S. VENEZUELAE BUT NOTHING IS KNOWN ABOUT THEIR BIOLOGICAL SIGNIFICANCE. AN INTRIGUING POSSIBILITY SUPPORTED BY IDENTIFICATION OF ACETYL AND SUCCINYL COA ESTER CONJUGATES TO RNA IS THAT THEY ARE INVOLVED IN RNA MEDIATED MANIPULATION OF SMALL MOLECULE METABOLISM. WE WILL ESTABLISH THE IDENTITIES OF COA RNA CONJUGATES IN MULTIPLE BACTERIAL SPECIES USING AN AFFINITY CAPTURE STRATEGY SIMILAR TO ONE USED RECENTLY TO IDENTIFY NAD RNA CONJUGATES IN E. COLI. WE WILL ALSO DETERMINE SEQUENCE AND SECONDARY STRUCTURE REQUIREMENTS FOR CONJUGATE FORMATION AND USE THIS INFORMATION TO ESTABLISH PHYLOGENETIC DISTRIBUTIONS OFCOA RNA AMONG SEQUENCED GENOMES. OUR RESULTS WILL PROVIDE THE FIRST CLEAR PICTURE OF THIS PREVIOUSLY UNRECOGNIZED FACET OF RNA BIOLOGY AND THEY WILL ENABLE FUTURE STUDIES EXPLORING THEIR BIOLOGICAL ROLES. SOME OF THE IDENTIFIED TRANSCRIPTS MAY REPRESENT TRUE MOLECULAR FOSSILS HELD OVER FROM THE TIME OF AN RNA WORLD OTHERS WILL BE NEWER INVENTIONS THAT ILLUSTRATE THE VARIETY OF WAYSIN WHICH ORGANISMS EXPLOIT RNA TRANSCRIPTS TO MANIPULATE SMALL MOLECULE METABOLITES. THUS THESE STUDIES ARE HIGHLY RELEVANT TO UNDERSTANDING THE EVOLUTION OF METABOLIC DIVERSITY OF EXTANT LIFE ON EARTH. AIM 2 ARTIFICIAL FAD RNA CONJUGATES. ENZYMES ENHANCE THE CHEMICAL REACTIVITY OF COFACTORS THROUGH BOTH COVALENT AND NON COVALENT INTERACTIONS. WE RECENTLY IDENTIFIED RNA APTAMERS THAT STRONGLY DIFFERENTIATE BETWEEN OXIDIZED FAD AND REDUCED FADH2 FLAVINS. WE WILL EXAMINE BOTH NON COVALENT AND COVALENT FLAVIN RNA COMPLEXES FOCUSING ON ESTABLISHING HOW THEIR MOLECULAR INTERACTIONS INFLUENCE INTRINSIC CHEMICAL REACTIVITY OF THE BOUND FLAVIN AND THE STRUCTURAL BASIS FOR THESE INFLUENCES. DIFFERENTIAL BINDING ENERGY IS USED BY FLAVOPROTEIN ENZYMES TO PERTURB INTRINSIC REACTIVITY HALF REACTION REDUCTION POTENTIAL THUS PROVIDING A STRONG CHEMICAL RATIONALE FOR THIS APPROACH. THE RESULTS FROM THIS STUDY WILL PROVIDE CHEMICAL CONSTRAINTS ON HOW TO CONNECT MODERN RNA METABOLITE CONJUGATES WITH THEIR POTENTIAL BIOCHEMICAL ROLES IN ANCIENT AND MODERN? METABOLISMS. THESE STUDIES WILL ADDRESS LONG STANDING MODELS FOR THE EVOLUTIONARY ORIGIN OF NUCLEOTIDE COFACTORS IN WHICH THESE MOLECULES ARE PROPOSED TO HAVE ENHANCED THE CATALYTICREPERTOIRE OF ANCIENT RIBOZYMES. THE PROJECT IS HIGHLY RELEVANT TO NASAS EXOBIOLOGY AND EVOLUTIONARY BIOLOGY PROGRAM AND TO THE NRAS EARLY EVOLUTION OF LIFE ANDTHE BIOSPHERE AREA OF EMPHASIS. WE ANTICIPATE THAT THE PROJECT WILL PROVIDE CRITICAL ADVANCES RELATED TO UNDERSTANDING SMALL MOLECULE METABOLISM AND RNA BIOLOGY IN MODERN ORGANISMS AND TO UNDERSTANDING RNAS ABILITY TO PROVIDE METABOLIC CATALYSIS IN AN RNA WORLD. THUS THESE STUDIES ARE HIGHLY RELEVANT TO FIVE SPECIFIC AREAS OF INTEREST TO NASA 1 EARLY EVOLUTION OF LIFE AND THE NATURE OF THE MOST PRIMITIVE ORGANISMS 2 THE TRANSITION TO MODERN BIOCHEMISTRY 3 EVOLUTION OF GENES PATHWAYS AND MICROBIAL SPECIES 4 THE REPERTOIRE OF DEMONSTRATED RNA FUNCTIONS AND 5 CONSTRUCTION OF ARTIFICIAL CHEMICAL SYSTEMS TO TEST HYPOTHESES REGARDING THE ORIGINAL NATURE OF KEY BIOLOGICAL PROCESSES.

$873,319
University Of Missouri System · · FY2017 · National Aeronautics and Space Administration

Lipidomics Biomarkers Link Sleep Restriction to Adiposity Phenotype, Diabetes, and Cardiovascular Risk

$873,305
Bruce S Kristal · Brigham And Women'S Hospital · R01 · FY2018 · HL

Using Integrative Genomics To Identify and Characterize Emphysema-Associated eQTL

$873,201
Peter Castaldi · Brigham And Women'S Hospital · R01 · FY2014 · HL