Scientific Areas of Integrated Review Groups (IRGs)

For a listing of the Scientific Review Administrator and membership roster for each study section, click on the study section roster under the study section name within the IRG shown below or go to the study section index (study sections listed alphabetically) and click on the specified roster next to the name of the study section.

Referral & Review

Genes, Genomes and Genetics IRG [GGG]               


The Genes, Genomes and Genetics [GGG] IRG will review research applications on fundamental and applied aspects of genes, genomes and genetics of humans and other organisms. Areas considered are fundamental mechanisms and regulation of gene expression, including chromosome function and maintenance, the regulation of DNA and RNA metabolism, translation, and posttranslational modification. Genomic studies, computational biology and technology development will also be considered, including development of new genetic tools and resources, global analysis of genetic systems, biological and computational resource development, and classification, storage, access, analysis and integration of genetic and other biological information. Genetic variation and evolution will be reviewed under the GGG IRG including the description, analysis and modeling of induced and natural genome variation, and comparisons between species. All aspects of quantitative genetics including complex trait mapping will be considered in humans and a wide variety of other species. The involvement of genetics in human health and disease will be considered, including the discovery, application and interpretation of gene and genomic variation influencing phenotype and the development of experimental and computational approaches to the identification of disease-related genes. Proposals dealing with model systems of all organisms, as they relate to human health and disease, will be considered, as will translational genetic studies applying fundamental genetic insight into the clinical setting.

The following Study Sections are included within the GGG IRG:  

Molecular Genetics A, B & C [MG - A, B & C]
Genomics, Computational Biology and Technology  [GCAT]
Genetic Variation and Evolution  [GVE]  
Genetics of Health and Disease [GHD]
Gene Therapy and Inborn Errors [GTIE] Special Emphasis Panel
Ethical, Legal and Social Implications of Human Genetics [ELSI-1]
Genes, Genomes and Genetics Small Business Activities [SBIR/STTR] Special Emphasis Panel [GGG Small Business SEP]
Genomics, Genetics, DNA Replication, and Gene Expression Fellowship Study Section [F08] 


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Molecular Genetics A, B and C Study Sections [MG - A, B and C]

[MG-A Roster] [MG-B Roster] [MG-C Roster]

The Molecular Genetics study sections will review grant applications on the fundamental mechanisms and regulation of gene expression. This will include chromosome function and maintenance, chromatin structure and remodeling, DNA replication, recombination and repair, transcription, RNA processing, translation, and post-translational modification. Experimental approaches may include the use of whole organism, cell-culture, or cell-free studies, structural analyses, genomic technologies, chemical genetics, and informatics. While all three study sections will review applications on eukaryotic organisms, crosscutting studies on prokaryotes where results may be broadly applicable across kingdoms will be clustered in the Molecular Genetics A study section with related topics such as DNA repair and mutation.

Specific areas covered by MG - A, B & C:

MGA

·         Chromatin structure and remodeling

·         DNA replication and cell cycle control

·         DNA repair pathways

·         Transcription mechanisms and regulation

·         RNA processing and stability

·         Protein synthesis and translational control

·         Post-translational processes

·         Protein ubiquitinylation and degradation

 

Additional areas may include:

·         Prokaryotic molecular genetics

·         Ribonucleoprotein assembly and transport

·         Non-coding RNA

·         Recombination

·         Mutagenesis

·         Extrachromosomal and organelle genetics

·         Mobile genetic elements

 

MGB

·         Chromatin structure and remodeling

·         DNA replication and cell cycle control

·         DNA repair pathways

·         Transcription mechanisms and regulation

·         RNA processing and stability

·         Protein synthesis and translational control

·         Post-translational processes

·         Protein ubiquitinylation and degradation

 

Additional areas may include:

·         Imprinting

·         Dosage compensation

·         Epigenetic processes

·         Ribonucleoprotein assembly and transport

·         Non-coding RNA

·         Gene regulatory networks

 

MGC

·         Chromatin structure and remodeling

·         DNA replication and cell cycle control

·         DNA repair pathways

·         Transcription mechanisms and regulation

·         RNA processing and stability

·         Protein synthesis and translational control

·         Post-translational processes

·         Protein ubiquitinylation and degradation

 

Additional areas may include:

·         Chromosome dynamics and structure

·         Meiosis and segregation

·         Cytogenetics

·         Recombination

·         Mutagenesis

·         Extrachromosomal and organelle genetics

·         Mobile genetic elements

 

 

The MG study sections have the following shared interests within the GGG IRG:

 

·         With Genomics, Computational Biology and Technology [GCAT]: Studies that apply high-throughput, computational, and/or mathematical modeling approaches to processes covered by the Molecular Genetics study sections could be assigned to MG-A, -B, or -C as appropriate. Development of emerging high-throughput, computational, network modeling, or mathematical approaches may be more appropriate for assignment to GCAT.

·         With Genetic Variation and Evolution [GVE]: Studies addressing mechanistic questions about mutation, recombination, and chromosome dynamics could be directed to MG-A, -B, or -C as appropriate. Studies with emphasis on evolutionary aspects, including statistical and quantitative methods, could be directed to GVE.

 

·         With Genetics of Health and Disease [GHD]: Cytogenic studies relating to diagnosis or disease processes could be assigned to GHD.  Studies that address fundamental questions about chromosome structure and organization could be assigned to MG. Studies on imprinting, X-inactivation, organelle genetics, recombination and DNA repair could be assigned to GHD if the emphasis is on genetic disease, and applications with a distinct human genetic focus could be assigned to GHD. If the focus is on molecular mechanisms, the application could be assigned to MG.  

 

 

The MG study sections have the following shared interests outside the

GGG IRG:

The MG study sections have shared interests in the study of genetic mechanisms with many IRGs. Applications that focus on fundamental mechanisms and/or regulation of DNA metabolism or gene expression could generally be assigned to MG-A, -B, or -C. Studies that employ a particular organ, system or disease as a model for investigating basic genetic processes may be appropriate for MG.

 

 

·         With the Biological Chemistry & Macromolecular Biophysics [BCMB] IRG: Shared interests include protein-nucleic acid interactions, nucleic acid enzymology, and structure/function studies of related macromolecular complexes. If the emphasis is on enzyme kinetics, detailed chemical reaction mechanisms, or high-resolution structure determination, the application could be assigned to BCMB. If structural analysis is one of several approaches to elucidate molecular genetic mechanisms, assignment could be to MG-A, -B, or -C.

 

·         With the Cell Biology [CB] IRG:  Shared interests include chromosome duplication and dynamics, nucleocytoplasmic trafficking, and signal transduction pathways. If the focus is on molecular genetic mechanisms and/or regulation of DNA metabolism or gene expression, studies on nuclear transport, cell cycle control, apoptosis, and signaling pathways may be assigned to the MG-A, -B, or -C study sections. Studies focusing on mitotic processes or on cytoskeletal or nuclear envelope assembly and dynamics may be assigned to CB.

 

·         With the Biology of Development & Aging [BDA] IRG: Shared interests include regulation of differentiation and cell fate determination. Studies on fundamental molecular genetic questions of broad biological significance could be assigned to MG. Studies on genetic control of development and aging could be assigned to BDA.

 

·         With the Infectious Diseases & Microbiology [IDM] and AIDS & Related Research [AARR] IRGs:  Genetic studies of microbes where the results principally apply to microbes could be assigned to IDM or AARR. Genetic studies where the results apply broadly across kingdoms could be assigned to MG, particularly MGA.

 

·         With the Oncological Sciences [ONC] IRG:  Molecular genetic studies of cancer etiology, tumor pathogenesis, or organ-specific carcinogenesis could be assigned to ONC. Basic mechanistic studies of genetic stability, DNA repair, or of cell growth control and differentiation could be assigned to MG-A, -B, or -C.

 

·         With the Organ-system/Disease IRGs - Hematology [HEME]; Cardiovascular Sciences [CVS]; Endocrinology, Metabolism, Nutrition, & Reproductive Sciences [EMNR]; Musculoskeletal, Oral, & Skin Sciences [MOSS]; Digestive Sciences [DIG]; Respiratory Sciences [RES]; and Renal & Urological Sciences [RUS]: Assignment of a molecular genetics application to an organ-system/disease IRG or to MG-A, -B, or -C should be based on the nature of the scientific question(s) being addressed.  Studies directed at a single organ-system or disease could be assigned to the organ-system or disease IRG, even if basic approaches are used.  Assignment could be to the MG-A, -B, or -C if the question(s) addressed may be applicable to multiple diseases or organ systems, or if the study involves an emerging approach for which expertise resides in a MG study section.

 

·         With the Neuroscience IRGs - Molecular, Cellular & Developmental Neuroscience [MDCN]; Integrative, Functional, & Cognitive Neuroscience [IFCN]; and Brain Disorders & Clinical Neuroscience [BDCN]: Applications with a primary focus on molecular genetic processes could be reviewed by the MG-A, -B, or -C study sections. However, applications with a primary focus on neuroscience processes could be reviewed by one of the neuroscience IRGs. The distinction is whether neuroscience questions are being asked or whether the nervous system is being used as a convenient model.

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Genomics, Computational Biology and Technology Study Section [GCAT]

[GCAT Roster]

The Genomics, Computational Biology and Technology Study Section will consider research applications involving global and integrative analyses of biological systems, and the development of new computational and experimental methodologies.  These would include (1) large-scale projects providing genetic information or resources, (2) functional and comparative genomics, (3) the application of bioinformatics and computational methods for collection, storage, integration, analysis, modeling and dissemination of genetic information, and (4) the development and validation of new experimental approaches applicable to systematic analyses.  These projects may pertain to humans or model systems.

Specific areas covered by GCAT:

  • Large-scale genetic analyses (e.g., microarrays, genomics, genome sequencing, gene identification, and chemical genetics)
  • Large-scale genetic resources (e.g., collections of mutant strains and lines, tagged genes, and small molecule probes)
  • Comprehensive studies of specific systems (e.g., cell cycle, signal transduction, metabolic control, and disease pathways)
  • Technology application for understanding simple and complex systems (single gene/protein as well as high throughput approaches)
  • Computational and mathematical representation and simulation of genetic systems (e.g., genetic networks, signaling, physiology, and host-pathogen interactions)
  • Analysis, mining, and integration of genetic data, including the development of new algorithms and statistical genetic methods
  • Classification and annotation systems for genetic data
  • Data storage, databases, and access to genetic information (e.g., user interfaces)
  • Development of model organisms/systems for genetic, genomic, or high-throughput analyses

 

 

GCAT has the following shared interests within the GGG IRG:

In general the GCAT study section could review applications pertaining to new and emerging technologies, large-scale/high throughput studies, and computational modeling of genetic systems.  Applications using established technologies applied to specific problems should be reviewed by other study sections.

 

  • With Molecular Genetics A, B, or C [MG-A, -B, or -C]: Studies that apply high-throughput, computational, and/or mathematical modeling approaches to processes covered by the Molecular Genetics study sections could be assigned to MG-A, -B, or -C as appropriate. Development of emerging high-throughput, computational, network modeling, or mathematical approaches may be more appropriate for assignment to GCAT.

  • With Genetic Variation and Evolution [GVE]: Large-scale studies of genetic variation and comparative genomics are shared interests. If studies are directed principally at understanding evolutionary processes or gene and genome evolution, including statistical methods, they could be assigned to GVE. If studies are directed principally at understanding such genetic or genomic questions as new and emerging genetic approaches, high throughput efforts, or computational modeling of genetic systems, they could be assigned to GCAT.

  • With Genetics of Health and Disease [GHD]: Genome scale studies applying workable technologies and approaches to human diseases may be appropriate for assignment to the GHD study section. Large-scale genomic and global studies may be appropriate for assignment to the GCAT study section.



GCAT has the following shared interests outside the GGG IRG:

 

  • With the Biological Chemistry & Macromolecular Biophysics [BCMB], Cell Biology [CB], Biology of Development & Aging [BDA], Oncological Sciences [ONC], Immunology [IMM], and Infectious Diseases & Microbiology [IDM] IRGs Projects reviewed by GCAT may be pertinent to all areas of biology.  For example, Biological Chemistry & Macromolecular Biophysics, Cell Biology and Biology of Development & Aging will cover topics related to the basic analysis of gene function, and other IRGs will cover aspects of genomics, proteomics, computational biology and technology related to specific organs and diseases. GCAT could review applications pertaining to new and emerging technologies, large-scale or high throughput studies, and computational modeling of genetic systems. Applications using established technologies applied to specific problems could be reviewed by other IRGs.

 

  • With the Bioengineering Sciences & Technologies [BST] IRG: Overlap is anticipated in the areas of statistical genetics, bioinformatics, and databases. If the focus is modeling technology or related analyses, bioinformatics or database technology, related computational analyses, or statistical methods for analyzing data, assignment to BST may be appropriate. If the focus is experimental, computational, or statistical investigation of questions related to genetics, regulation of gene expression, or genomics, assignment to GCAT may be appropriate.

 

  • With the Health of the Population [HOP] IRG: Applications with a primary focus on the genetic etiology of a disease could be reviewed by the GCAT study section. Applications with a primary focus on genetics as a risk factor in an epidemiologic study could be reviewed by HOP.

 

  • With the Organ-system/Disease IRGs - Hematology [HEME]; Cardiovascular Sciences [CVS]; Endocrinology, Metabolism, Nutrition, & Reproductive Sciences [EMNR]; Musculoskeletal, Oral, & Skin Sciences [MOSS]; Digestive Sciences [DIG]; Respiratory Sciences [RES]; and Renal & Urological Sciences [RUS]: Assignment of a gene/genomics/genetics application to an organ-system/disease IRG or to GCAT should be based on the nature of the scientific question(s) being addressed.  Studies directed at a single organ-system or disease could be assigned to the organ system or disease IRG, even if basic approaches are used.  Assignment could be to GCAT if the question(s) addressed may be applicable to multiple diseases or organ systems, or if the study involves an emerging approach for which expertise resides in GCAT.

 

  • With the Neuroscience IRGs - Molecular, Cellular & Developmental Neuroscience [MDCN]; Integrative, Functional, & Cognitive Neuroscience [IFCN]; and Brain Disorders & Clinical Neuroscience [BDCN]: Applications with a focus on large-scale gene/genomic/genetic studies could be reviewed by the GCAT study section. Applications with a focus on neuroscience processes could be reviewed by MDCN, IFCN, or BDCN.

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Genetic Variation and Evolution Study Section [GVE]

 

[GVE Roster]

 

The Genetic Variation and Evolution Study Section addresses grant applications related to the origin, distribution, maintenance, and effects of genetic variation.  It considers studies ranging from characterization of the genetic and phenotypic differences among individuals and species to the evolution of genomes and biological systems.

Specific areas covered by (but not limited to) GVE:

  • Description and modeling of the levels and patterns of variation
  • Analysis of induced and natural variation for Mendelian and complex traits
  • Genotype-phenotype associations
  • Use of natural variation for gene discovery and functional genomics
  • Genetics of speciation
  • Adaptive evolution
  • Chromosome evolution
  • Evolution and organization of genomes, including gene duplication, repetitive elements, and multigene families
  • Evolution of gene regulation and regulatory circuits
  • Evolution of development
  • (Co) evolution of hosts and their symbionts/pathogens
  • Genetic variation and environmental factors

 

These topics will be investigated in a variety of species, including humans, other animals, plants, and microbes. Approaches include molecular genetics; quantitative trait locus analysis, linkage and association mapping; experimental and theoretical population genetics; experimental or simulated evolution; phylogenetics; molecular evolutionary analysis; comparative genomics; gene expression and protein analyses.

 

GVE may welcome applications that attempt to dissect complex morphological, behavioral, physiological and fitness-related phenotypes. Proposals to be considered may also include the development of statistical methods for inferring evolutionary processes or mapping quantitative traits; development of new model systems relevant to these topics; community-wide resources, such as database and computational tools; and modeling the emergence of naturally occurring or intentionally released infectious diseases, including genetic, evolutionary and ecological mechanisms and interactions.

 

GVE has the following shared interests within the GGG IRG:

 

  • With Molecular Genetics-A, -B, & -C [MG-A, -B, & -C]: Studies addressing mechanistic questions about mutation, recombination, and chromosome dynamics could be directed to MG-A, -B, or -C as appropriate. Studies with emphasis on evolutionary aspects could be directed to GVE.

 

  • With Genomics, Computational Biology and Technology [GCAT]: Large-scale studies of genetic variation and comparative genomics are shared interests. If studies are directed principally at understanding evolutionary processes or gene and genome evolution, including statistical methods, they could be assigned to GVE. If studies are directed principally at understanding such genetic or genomic questions as new and emerging genetic approaches, high throughput efforts, or computational modeling of genetic systems, they could be assigned to GCAT.

 

  • With Genetics of Health and Disease [GHD]: Genetic variation and complex trait mapping are shared interests. GVE may be appropriate for applications emphasizing evolutionary aspects of complex trait analysis and comparative genomics, including experimental, statistical, and theoretical methods. GHD may be more appropriate for applications emphasizing human variation in disease.

 

GVE has the following shared interests outside the GGG IRG:

 

  • With the Biology of Development & Aging [BDA] IRG: Shared interests are in the study of the genetic variation of aging and the evolution of development. If the primary focus is to characterize natural variation or test evolutionary models or to elucidate evolutionary processes, the application could be assigned to GVE. An application using established genetic technologies applied to specific questions of development or aging could be assigned to BDA.

 

  • With the Bioengineering Sciences & Technologies [BST] IRG: Shared interests include computational methods and informatics. Applications specifically addressing statistical and computational analyses of genetic variation or evolution could be reviewed by GVE. Applications addressing broader statistical and computational questions could be reviewed by the BST IRG.

 

  • With the Immunology [IMM] IRG: Proposals addressing genetic variation and evolution of immune responses could be reviewed by GVE. Applications using established genetic technologies applied to immunological problems could be reviewed by IMM.

 

  • With the Infectious Diseases & Microbiology [IDM] and AIDS & Related Research [AARR] IRGs: Applications specifically addressing genetic variation and evolution of infectious agents could be reviewed by GVE. Applications using established genetic technologies applied to the study of specific infectious agents could be reviewed by IDM/AARR.

 

 

  • With the Organ-system/Disease IRGs - Hematology [HEME]; Cardiovascular Sciences [CVS]; Endocrinology, Metabolism, Nutrition, & Reproductive Sciences [EMNR]; Musculoskeletal, Oral, & Skin Sciences [MOSS], Digestive Sciences [DIG], Respiratory Sciences [RES], and Renal & Urological Sciences [RUS]: Assignment of a genetic analysis of complex traits application to an organ-system/disease IRG or to GVE should be based on the nature of the scientific question(s) being addressed.  Studies directed at a single organ-system or disease could be assigned to the organ system or disease IRG, even if basic approaches are used.  Assignment could be to GVE if the question(s) addressed may be applicable to multiple diseases or organ systems, or if the study involves an emerging approach for which expertise resides in GVE. Thus, proposals mapping genes affecting variation in complex traits could be considered by GVE; applications emphasizing functional and mechanistic studies could be assigned to the appropriate disease or organ system IRG.

 

  • With the Neuroscience IRGs - Molecular, Cellular & Developmental Neuroscience [MDCN]; Integrative, Functional, & Cognitive Neuroscience [IFCN]; and Brain Disorders & Clinical Neuroscience [BDCN]: Applications with a focus on genetic variation or evolution could be reviewed by the GVE study section. However, applications with a primary focus on neuroscience processes could be reviewed by MDCN, IFCN, or BDCN.

 

 

Genetics of Health and Disease Study Section [GHD]

 

[GHD Roster]

 

The GHD Study Section will review applications involving the discovery, application and interpretation of genetic and genomic variation in human phenotype and disease.

 

 

Specific areas covered by GHD:

 

 

  • Genetic basis of Mendelian and non-Mendelian human diseases
  • Mapping and identification of normal and disease phenotypes, including those associated with rare disorders
  • Genetic and epigenetic phenomena such as imprinting, X inactivation, repeat expansions, genetic recombination and DNA repair, where genetic disease is emphasized
  • Non-Mendelian traits including mitochondrial and organelle diseases
  • Quantitative genetics of complex traits, genetic dissection, including QTL (quantitative trait locus) mapping
  • Disease-related variations including SNPs (single nucleotide polymorphisms) and haplotypes
  • Cytogenetics and chromosome disorders
  • Genome architecture and genomic disorders
  • Pharmacogenetics and biochemical genetics, including inborn errors of metabolism
  • Interaction of the genome with exogenous factors including environment and maternal genotype
  • Explicit models of human diseases, including mouse, Drosophila, zebra fish, and other organisms
  • Genetic, pre-implantation and prenatal diagnostics
  • Therapeutic approaches to genetic disease including gene and protein replacement therapy
  • Translational genetics, including outcome studies concerning genotype-phenotype correlation and the application of fundamental genetics to clinical practice
  • Genetic epidemiology, population and newborn screening, and public health applications of genetics

 

GHD has the following shared interests within the GGG IRG:

 

  • With Molecular Genetics-A, -B, & -C [MG-A, B, & -C]: Cytogenetic studies relating to diagnosis or disease processes could be assigned to GHD. Studies that address fundamental questions about chromosome structure and organization could be assigned to MG. Studies on imprinting, X-inactivation, organelle genetics, recombination and DNA repair could be assigned to GHD if the emphasis is on genetic disease. If the focus is on molecular mechanisms, such applications could be assigned to MG.

 

  • With Genomics, Computational Biology and Technology [GCAT]: Genome scale studies applying workable technologies and approaches to human diseases may be appropriate for assignment to the GHD study section. Large-scale genomic and global studies may be appropriate for assignment to the GCAT study section.

 

  • With Genetic Variation and Evolution [GVE]: Genetic variation and complex trait mapping are shared interests. GVE may be appropriate for applications emphasizing evolutionary aspects of complex trait analysis and comparative genomics, including experimental, statistical, and theoretical methods. GHD may be more appropriate for applications emphasizing human variation in disease.