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Archived File. The file below has been archived for historical reference purposes only. The content and links are no longer maintained and may be outdated. See the OER Public Archive Home Page for more details about archived files. PEER REVIEW ADVISORY COMMITTEE
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Archived File The file below has been archived for historical reference purposes only. The content and links are no longer maintained and may be outdated. See the OER Public Archive Home Page for more details about archived files.
PEER REVIEW ADVISORY COMMITTEE Update on New CSR Realignments Basic Oncology and Bioengineering Don Schneider February 1, 2010 National Institutes of HealthU.S. Department of Health and Human Services
Continuous evolution/alignment of study sections is necessary • Science changes • CSR is committed to assessment • Study section size matters – too small/too large [Fewer than 50 applications Is a problem]
Three goals to consider • Look at recent reorganizations • Examine proposed guideline adjustments for Oncology 1 – Basic Translational (OBT) IRG • Re-examine Microscopic Imaging study section
Cell Biology merged study sections 2009/05 2010/05 Cell Structure Nuclear & Cytoplasmic & Function 41 Struct, Functn, & Dynam Nuclear Dynam 67 & Transport 45 Cellular Signaling Cellular Signaling & Regulatory & Regulatory Systems 58 Systems 84 Subtotal 144 151 applctns
Digestv, Kidney, & Urologcl Sys merged study sections 2009/05 2010/05 Gastrointestinal Cell & Molecular Biology 41 Gastrointestinal Gastrointestinal Mucosal Mucosal Pathobiology 53 Pathobiology 56 Hepatobiliary Hepatobiliary Pathophysiology 64 Pathophysiology 78 Clinical &Clinical, IntegrativeIntegrative Gastrointestinal& Molecular Pathobiology 46Gastroenterology 68 Subtotal 204 202
Bioengineering merged panels 2009/05 2010/05 Biodata Management Biodata Management & Analysis 40 & Analysis 88 SEP 28 Modeling & Analysis Modeling & Analysis Of Biological Of Biological Systems 39 Systems 72 Microscopic Microscopic Imaging 20 Imaging 27 Subtotal 127 187
Interim analysis of realignments is positive • Workloads improve (except Micros Imaging) • Science and fairness of review are probably better • CSR needs metric/tool to measure scientific impact
AIDS, Behavioral and Population Sciences Basic and Integrative Biological Sciences Physiological and Pathological Sciences Translational and Clinical Sciences Neuroscience, Development and Aging Biobehavioral & Behavioral Processes Biological Chemistry & Macromolecular Biophysics Endocrinology, Metabolism, Nutrition & Reproductive Sciences Cardiovascular and Respiratory Sciences Brain Disorders & Clinical Neuroscience Risk, Prevention& Health Behavior Surgical Sciences, Biomedical Imaging and Bioengineering Molecular, Cellular & Developmental Neuroscience Bioengineering Sciences & Technologies Immunology Population Sciences & Epidemiology Integrative, Functional & Cognitive Neuroscience Cell Biology Infectious Diseases & Microbiology Musculoskeletal, Oral & Skin Sciences Healthcare Delivery & Methodologies Genes, Genomes & Genetics Oncology: Translational Clinical Emerging Technologies & Training in Neuroscience Digestive, Kidney & Urological Systems AIDS & AIDS Related Research Oncology: Basic Translational Vascular and Hematology Biology of Development & Aging Interdisciplinary Molecular Sciences & Training CSR formed five review divisions, January 2009
Oncology 1 – Basic & Translational IRG was established and reviewed • Split ONC to form OBT & OTC January 2009 • Collected feedback from reviewers two cycles (October and February meetings) • Discussed feedback with Chairs (Chief and DD) • Reviewed by CSR Director et al September 23, 2009 [Chief – Cathleen Cooper]
Realignments are proposed for OBT study sections For emerging trends, clarity of scientific scope, and workload balance, guideline adjustments are proposed: • Cancer Molecular Pathology study section (CAMP) –about 110 applications a cycle; focuses on oncogenes and tumor suppressors; move telomeres and epigenomics • Cancer Genetics study section (CG) – about 75 applications a cycle; focuses on chromosomal integrity and stability; add telomeres and epigenomics (would fit well) • Cancer Etiology study section (CE) – about 90 applications a cycle; focuses on DNA repair and environmental carcinogenesis; move epigenomics unless focus is environmental • Estimated result: about 95, 90, and 90 applications
Bioengineering Sciences and Technologies IRG was formed in 2004 Regular Study Sections • Biodata Management and Analysis (BDMA) • Biomaterials and Biointerfaces (BMBI) • Gene and Drug Delivery Systems (GDD) • Instrumentation Systems and Development (ISD) • Modeling and Analysis of Biological Systems (MABS) • Microscopic Imaging (MI) • Nanotechnology (NANO) [Chief – George Chacko]
Steps to realign were taken a year ago • Original study sections were hybrids in that R01s and R43s were reviewed together – no longer possible • BDMA & MI were small, about 50 applications each • Via Working Group and PRAC, BDMA was combined with a software SEP and scope of MI was expanded
Microscopic Imaging and Spectroscopy The study section focuses on review of applications on techniques and instrumentation for microscopic visualization of molecules, organelles, and model systems • Development and improvement of microscopic imaging and spectroscopy • Development of imaging tools/software • Image acquisition and analysis, including single particle
Instrumentation Systems and Development shares interests with Microscopic Imaging • Optical and spectroscopic instrumentation • Microfabrication • Automation and integration • Sensing of single cells
MIS, ISD, & EBT share interests • Microscopic Imaging and Spectroscopy, in BST, focus is to develop techniques to visualize molecules, organelles, and cells • Instrumentation and Systems Development, in BST, focus is to develop instrumentation for biological research • Enabling Bioanalytical and Biophysical Technologies, in BCMB, focus is development of bioanalytical tools to probe molecules
Options presented to Working Group [Working within the Bioengineering IRG] • Terminate MIS • Merge MIS with ISD • Expand the scope of MIS
Bioengineering Working Group #2 met January 2010 ROSTER • Wah Chiu, PhD (Baylor College of Medicine) • Robert M Dickson, PhD (Georgia Institute of Technology) • Michael Gilson, MD, PhD (University of Maryland) • Enrico Gratton, PhD (University of California Irvine) • Jerome Mertz, PhD (Boston University) • Stephen C Miller, PhD (University of Massachusetts Worcester) • Amy Palmer, PhD (University of Colorado Boulder) • Peter Sorger, PhD (Massachusetts Institute of Technology) • Shankar Subramaniam, PhD (University of California San Diego) • Stephen Wong, PhD (Cornell University Weill) • Xiaowei Zhuang, PhD (Harvard University) • NIH: James Deatherage, PhD (NIGMS); Catherine Lewis, PhD (NIGMS); George Chacko, PhD (CSR); Don Schneider, PhD (CSR)
Working Group Expressed Preferences • Terminate Microscopic Imaging - WG least enthusiasm, integrated basic imaging panel has value, will grow • Merge MIS, principally with Instrumentation and Systems Development - WG medium enthusiasm • Expand scope and continue Microscopic Imaging - WG considerable enthusiasm
Should MI be continued? • Element of “Been there, done that” • Related issues - EBT study section - IMST IRG
CSR created Interdisciplinary Molecular Sciences & Training IRG January 2009 • IMST uses SEPs to review all fellowship and small business applications for Basic & Integrative Biological Sciences (basic oncology, bio-chemistry/biophysics, bioengineering, cell biology, and genetics) • IMST uses SEPs to review interdisciplinary special applications, e.g., some P01s, P41s, and S10s • IMST was recently chartered, with understanding that it would form a regular, chartered study section [Chief – Ross Shonat]
Taking a bolder, broader view • EBT averages about 60 applications a round • MI averages about 25 applications a round • EBT and MI have complementary interests • IMST IRG needs a chartered study section • 25 + 60 = 85, close to ideal • Create EBIT, Enabling Bioanalytical and Imaging Technologies
PRAC input sought Oncology 1 – Basic Translational IRG (OBT) • Move telomeres and epigenomics from Cancer Molecular Pathology to Cancer Genetics • Move some epigenomics from Cancer Etiology to Cancer Genetics Microscopic Imaging and Spectroscopy • Allow more time for growth, OR • Merge with Enabling Bioanalytical and Biophysical Technologies and move to Interdisciplinary Molecular Sciences and Training IRG