? BIOINFORMATICS SHARED RESOURCE The Bioinformatics (BIn) shared resource, a core function of the Duke Cancer Institute (DCI), serves as a centralized resource for expertise in applied and theoretical cancer bioinformatics, genomics, computational biology, machine learning and statistical genetics. The faculty and staff members of this shared resource support DCI members across the continuum of research, including experimental and statistical design for genomic studies, complex genomic data management, integration of diverse data sets, computing and statistical analysis, and machine learning. The shared resource provides support for investigator-generated data as well as retrospective data from research databases (e.g., GDC [large datasets like TCGA] or dbGAP). The resource?s mission is to provide high-quality, service-oriented, coordinated and cost-efficient bioinformatics support and infrastructure for DCI members. Emphasis is placed on facilitating increased collaborations across DCI programs and other DCI shared resources. The mission of this shared resource is addressed within the framework of adherence to 3 principles: 1- sound data provenance and statistical principles, 2- literate programming, and 3- reproducible analysis. The BIn shared resource provides and runs standardized genomic analysis pipelines (e.g., germline, tumor and cell-free DNA-Seq, bulk and single-cell RNA-Seq, CHiP-Seq, and sequencing of T-Cell Receptor repertoire and microbiome). These pipelines are constructed on the basis of state-of-the-art published tools, maintained under strict source code version control and designed to be extensible and deployable in a scalable fashion on local servers and cloud services. The philosophy of the BIn shared resource is that the scope of scientific discovery and rigor should neither be limited nor compromised due to lack of appropriate and adequate statistical methodology or computational tools. When needed and appropriate, the faculty and staff of the shared resource extend or revise existing or develop de novo methods and computational tools to enable DCI members to address scientific questions with requisite rigor and efficiency. In addition to computing and analysis support, the shared resource provides extensive support for writing of scientific abstracts and manuscripts, as well as grant proposals. The BIn shared resource also serves as a liaison and facilitator between DCI members and other DCI shared resources (e.g., the Biostatistics, Functional Genomics, Information Systems, and BioRepository and Precision Pathology Center Shared Resources). The research support, services and resources of the BIn shared resource are provided exclusively to DCI members. In 2018, the BIn shared resource provided services to 53 investigators, 100% of whom were DCI members, accounting for 100% of total usage, from all 8 DCI Research Programs. Use of this shared resource by DCI members contributed to 178 publications over the project period, 41 of which were in high impact journals, demonstrating the value of services offered by the resource.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014236-47
Application #
10118121
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-01-01
Project End
2024-12-31
Budget Start
2021-01-01
Budget End
2021-12-31
Support Year
47
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Dai, Ziwei; Mentch, Samantha J; Gao, Xia et al. (2018) Methionine metabolism influences genomic architecture and gene expression through H3K4me3 peak width. Nat Commun 9:1955
Powell Gray, Bethany; Kelly, Linsley; Ahrens, Douglas P et al. (2018) Tunable cytotoxic aptamer-drug conjugates for the treatment of prostate cancer. Proc Natl Acad Sci U S A 115:4761-4766
Abdi, Khadar; Lai, Chun-Hsiang; Paez-Gonzalez, Patricia et al. (2018) Uncovering inherent cellular plasticity of multiciliated ependyma leading to ventricular wall transformation and hydrocephalus. Nat Commun 9:1655
Hudson, Kathryn E; Rizzieri, David; Thomas, Samantha M et al. (2018) Dose-intense chemoimmunotherapy plus radioimmunotherapy in high-risk diffuse large B-cell lymphoma and mantle cell lymphoma: a phase II study. Br J Haematol :
Fayanju, Oluwadamilola M; Park, Ko Un; Lucci, Anthony (2018) Molecular Genomic Testing for Breast Cancer: Utility for Surgeons. Ann Surg Oncol 25:512-519
Porter, Laura S; Fish, Laura; Steinhauser, Karen (2018) Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention. J Pain Symptom Manage 56:252-258
Káradóttir, Ragnhildur T; Kuo, Chay T (2018) Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis. Annu Rev Neurosci 41:139-161
Han, Peng; Liu, Hongliang; Shi, Qiong et al. (2018) Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck. Mol Carcinog 57:784-793
Xu, Yinghui; Wang, Yanru; Liu, Hongliang et al. (2018) Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Mol Carcinog 57:22-31
Abdi, Khadar; Kuo, Chay T (2018) Laminating the mammalian cortex during development: cell polarity protein function and Hippo signaling. Genes Dev 32:740-741

Showing the most recent 10 out of 513 publications