GENOME AND SINGLE CELL TECHNOLOGIES The key function of The Jackson Laboratory Cancer Center (JAXCC) Genome and Single Cell Technologies Shared Resource (GSCT) is the provision of genomic technologies to sequence the genomic structures (DNA, RNA, epigenome) and to precisely define the molecular features of individual cells. GSCT is composed of two integrated components that are each part of JAX's institutionally managed Scientific Services program: Genome Technologies, led by Dr. Chia-Lin Wei, and Single Cell Biology, led by Dr. Paul Robson. GSCT provides a continuum of methods to address complex questions in cancer genomics and genomic biology. Key capabilities include a suite of molecular biology protocols; diverse platforms for DNA sequencing; and streamlined data management and analysis systems developed in conjunction with the Computational Sciences Shared Resource. Sequencing includes first generation Sanger sequencing, second-generation high-throughput short- read, and third-generation single molecule long-read sequencing services. The expansion of the Shared Resource to include Single Cell Biology broadens the repertoire of platforms to include droplet-based single cell transcriptomic and epigenomic sequencing. GSCT also continually develops new methods, and identifies and brings in the best externally developed methods, often in close collaboration with JAXCC members. GSCT keeps all JAXCC members abreast of the latest available technologies through seminars, workshops, one-on-one meetings, and directly through hands-on training of JAXCC member trainees. GSCT thus provides comprehensive, high quality and effective solutions for JAXCC members to profile cancers using whole genome, epigenome and transcriptome sequencing approaches and spatially resolved cellular phenotyping. In the next funding cycle, our goal is to continue to provide genomic and single cell technology support and ensure JAXCC members have access to the platforms they need to investigate the genomic instability and genetic complexity of cancer and the molecular interactions between a tumor and host that contribute to cancer biology.
Our Specific Aims are to: 1) Incorporate new efficiencies to improve GSCT operations and enhance value to JAXCC members; 2) Provide JAXCC members with new genomic technologies for multi-dimensional genome analyses; and 3) Provide the tools to dissect cellular heterogeneity of complex cellular systems.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA034196-34
Application #
9854058
Study Section
Subcommittee H - Clinical Groups (NCI)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
34
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
Cho, Sung-Yup; Sung, Chang Ohk; Chae, Jeesoo et al. (2018) Alterations in the Rho pathway contribute to Epstein-Barr virus-induced lymphomagenesis in immunosuppressed environments. Blood 131:1931-1941
Pullagura, Sri Ramulu N; Buaas, Bill; Gray, Nichelle et al. (2018) Functional Redundancy of DICER Cofactors TARBP2 and PRKRA During Murine Embryogenesis Does Not Involve miRNA Biogenesis. Genetics 208:1513-1522
Kong, Yang; Naggert, Jürgen K; Nishina, Patsy M (2018) The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina. Adv Exp Med Biol 1074:545-551
Chang, Bo; FitzMaurice, Bernard; Wang, Jieping et al. (2018) Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele. Invest Ophthalmol Vis Sci 59:5127-5139
Sharma, Manju; Braun, Robert E (2018) Cyclical expression of GDNF is required for spermatogonial stem cell homeostasis. Development 145:
Shi, Jiayuan; Hua, Li; Harmer, Danielle et al. (2018) Cre Driver Mice Targeting Macrophages. Methods Mol Biol 1784:263-275
Hosur, Vishnu; Farley, Michelle L; Low, Benjamin E et al. (2018) RHBDF2-Regulated Growth Factor Signaling in a Rare Human Disease, Tylosis With Esophageal Cancer: What Can We Learn From Murine Models? Front Genet 9:233
Johnson, Kenneth R; Gagnon, Leona H; Tian, Cong et al. (2018) Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice. Genetics 208:1165-1179
Dominguez, Pilar M; Ghamlouch, Hussein; Rosikiewicz, Wojciech et al. (2018) TET2 Deficiency Causes Germinal Center Hyperplasia, Impairs Plasma Cell Differentiation, and Promotes B-cell Lymphomagenesis. Cancer Discov 8:1632-1653
Paigen, Kenneth; Petkov, Petko M (2018) PRDM9 and Its Role in Genetic Recombination. Trends Genet 34:291-300

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