Our genomics-based scientists and their external collaborators are at a critical point in their research: now, and increasingly over the next years, their discoveries will be limited by the quantity and quality of computing and storage that they can access. While Mount Sinai has funded an excellent supercomputing and storage infrastructure along with professional staff to operate and maintain it, it has been a runaway success and it is now under-provisioned, negatively impacting its largest group of users the greatest: the genomics-based researchers. The scientific productivity of these researchers is greatly inhibited on this existing infrastructure due to long queue wait times especially during critical periods compounded by the extraordinary amount of time spent managing their data storage due to a substantial under-supply. With the explosion of progressively complex scientific and data queries planned by the 20 PIs, their 24 projects and their 55 external collaborating institutions comprising over $43 million in NIH funding, these limited resources are severely restricting the ability of the researchers to collaborate and to share their data with the broader scientific community. To enable these researchers instead to flourish, we propose a """"""""Big Omics Data Engine"""""""" (BODE) instrument: a dedicated, specialized data analytic supercomputer customized for Mount Sinai's specific scientific needs. Such an instrument will increase their throughput by at least 3X and up to 10X by using 2,484 Intel Haswell enterprise cores. The available storage space will expand by over 3X to 5 petabytes, thus greatly enhancing the genomics-based research in a spectrum of disease categories including autism, insulin resistance in diabetics, schizophrenia and related behavioral disorders, cardiac care, the origins of drug addiction and depression, and cancer progression. Moving the genomics researchers to a new machine will also have the secondary effect of freeing up compute cycles and storage on our existing supercomputer for our next highest demand group of users: the structural and chemical biology researchers. In recognition of the intense scientific need for this instrument, Mount Sinai has agreed to fund up to $4 million in operating costs.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10OD018522-01
Application #
8734830
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Klosek, Malgorzata
Project Start
2014-07-03
Project End
2015-07-02
Budget Start
2014-07-03
Budget End
2015-07-02
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Genetics
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Putzel, Gregory Garbès; Battistella, Giovanni; Rumbach, Anna F et al. (2018) Polygenic Risk of Spasmodic Dysphonia is Associated With Vulnerable Sensorimotor Connectivity. Cereb Cortex 28:158-166
Manasson, Julia; Shen, Nan; Garcia Ferrer, Helga R et al. (2018) Gut Microbiota Perturbations in Reactive Arthritis and Postinfectious Spondyloarthritis. Arthritis Rheumatol 70:242-254
Cruchaga, Carlos; Del-Aguila, Jorge L; Saef, Benjamin et al. (2018) Polygenic risk score of sporadic late-onset Alzheimer's disease reveals a shared architecture with the familial and early-onset forms. Alzheimers Dement 14:205-214
Marino, Kristen A; Filizola, Marta (2018) Investigating Small-Molecule Ligand Binding to G Protein-Coupled Receptors with Biased or Unbiased Molecular Dynamics Simulations. Methods Mol Biol 1705:351-364
Sun, Zhen; Filipescu, Dan; Andrade, Joshua et al. (2018) Transcription-associated histone pruning demarcates macroH2A chromatin domains. Nat Struct Mol Biol 25:958-970
Wojcik, Genevieve L; Fuchsberger, Christian; Taliun, Daniel et al. (2018) Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. G3 (Bethesda) 8:3255-3267
Hughes, Taylor E T; Lodowski, David T; Huynh, Kevin W et al. (2018) Structural basis of TRPV5 channel inhibition by econazole revealed by cryo-EM. Nat Struct Mol Biol 25:53-60
Wei, Xiaomu; Calvo-Vidal, M Nieves; Chen, Siwei et al. (2018) Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple Myeloma. Cancer Res 78:2747-2759
Fazlollahi, M; Chun, Y; Grishin, A et al. (2018) Early-life gut microbiome and egg allergy. Allergy 73:1515-1524
Manheimer, Kathryn B; Richter, Felix; Edelmann, Lisa J et al. (2018) Robust identification of mosaic variants in congenital heart disease. Hum Genet 137:183-193

Showing the most recent 10 out of 180 publications