New York Genome Center
Established | 2011 |
---|---|
Research type | Basic (non-clinical), Clinical research and translational research |
Field of research | Genomics, Bioinformatics, DNA sequencing, Whole genome sequencing |
President | Cheryl A. Moore[1] |
Location | New York City, New York, United States |
Affiliations |
|
Website | New York Genome Center |
The New York Genome Center (NYGC) is a 501(c)(3) nonprofit biomedical research organization in New York, New York.[3] A collaboration of academic, medical and industry leaders in New York and other partners throughout the country, the New York Genome Center focuses on translating genomic research into clinical solutions for serious diseases. NYGC faculty hold joint academic appointments at its member institutions and lead clinically focused genomic studies in a number of disease areas, including pediatric and adult cancer, asthma, autism, Alzheimer’s disease, ALS and other serious neurodegenerative diseases. NYGC scientists brings a multidisciplinary and in-depth approach to the field of genomics, conducting research in a wide range of areas, including single cell genomics, gene engineering, population and evolutionary genomics, technology and methods development, statistics, computational biology and bioengineering.[4]
Founding
The Center was legally founded in November 2011 as a collaboration among eleven academic institutions to advance genome research,[5] based on leadership from Tom Maniatis[6] and financial support of $2.5 million from each institution as well as a number of private philanthropists, including then Mayor Michael Bloomberg, James Simons and Russell Carson.[5] One year after its founding, NYGC recruited Robert B. Darnell as President and Scientific Director,[7] and formally opened in a newly built facility on September 19–20, 2013.[8][9]
From November 2012 to December 2016, the Center's President and CEO was Robert B. Darnell.[10][7] During this period, NYGC had a number of major accomplishments,[10] including the hiring of 17 full time and part time NYGC faculty,[11] award of a $40 million grant to Dr. Darnell as Principal Investigator from the National Human Genome Research Institute to create a Center for Common Disease focused on autism,[12] fundraising that included a $55 million grant from New York State to support genomic medicine,[13] a $100 million matching grant from the Simons Foundation and Carson Family Charitable Trust,[14][15] a $13.5 million contract from NHLBI, a PCORI grant to centralize clinical data in New York,[10] and collaborations with IBM to explore and develop the use of Watson for Genomics in glioblastoma[16] and more generally in cancer genomics.[17] As of 2016, though the majority of participating institutions remained New York state-based, two institutions were from outside New York: Jackson lab and Princeton University.
The 12 founding institutions (Albert Einstein College of Medicine joined the original 11 institutions on April 2013)[18] were:
- Cold Spring Harbor Laboratory (New York)
- Columbia University (New York)
- Cornell University / Weill Cornell Medical College (New York)
- Memorial Sloan Kettering Cancer Center (New York)
- Icahn School of Medicine at Mount Sinai (New York)
- New York—Presbyterian Hospital (New York)
- NYU School of Medicine (New York)
- Northwell Health (New York)
- The Jackson Laboratory (Maine)
- Rockefeller University (New York)
- Stony Brook University (New York)
- Albert Einstein College of Medicine (New York)
Facility
The Center has 170,000 square feet (16,000 m2) of space in a multi-story building at 101 Avenue of the Americas.[10][19] By the end of 2015, the Center had acquired 16 Illumina HiSeq X Ten and 12 HiSeq 2500 sequencing instruments.[20]
Finances and projects
As of 2016, the Center's revenue came from US and New York state governments, a contract with 10 medical institutes for central management of clinical data, and a couple of charitable foundations.[10] This includes funds pledged by the Simons Foundation and the Carson Family Charitable Trust of up to $100 million from 2016 to 2019.[14][15]
Government funding has included a $40 million grant in 2016 for establishing a Center for Common Disease Genomics from the National Human Genome Research Institute, the aim of which is to describe a comprehensive list of genes underlying common diseases.[15] Also in 2016, the Center and Weill Cornell Medicine received a National Cancer Institute grant to support a joint cancer genomics data center for the research and clinical interpretation of tumors, a part of the ongoing development of The Cancer Genome Atlas; the grant provides $490,000 per year for five years.[21]
In 2015, the Center won a $13.5 million contract to conduct whole genome sequencing and analysis for the National Heart, Lung, and Blood Institute's TOPMed program.[20][lower-alpha 1]
National Tumor Registry
In February 2016, the Center started a collaboration with IBM to create a tumor registry matching tumor characteristics and therapeutic responsiveness to genetic profiles among cancer patients.[10][22] The work has been part of the US Government Precision Medicine Initiative and has employed the Watson system.[10][22]
Two years prior to this, the Center and IBM collaborated on development of an early version of the tumor registry focused on glioblastoma multiforme,[23] utilizing a pre-production version of Watson Discovery Advisor.[24][25][26]
Notable associates
- Robert Darnell, Founding Director[7][10]
- Harold Varmus, senior associate core member[10][27][28]
- Michael Wigler, senior associate core member[29]
- Simon Tavaré, senior scientist[29]
Notes
- ↑ NYGC is among several recipients, another being the Broad Institute.
Recent Publications
- Willems, Thomas; Zielinski, Dina; Yuan, Jie; Gordon, Assaf; Gymrek, Melissa; Erlich, Yaniv (2017). "Genome-wide profiling of heritable and de novo STR variations". Nature Methods. 14 (6): 590–592. PMID 28436466. doi:10.1038/nmeth.4267.
- Villani, Alexandra-Chloé; Satija, Rahul; Reynolds, Gary; Sarkizova, Siranush; Shekhar, Karthik; Fletcher, James; Griesbeck, Morgane; Butler, Andrew; Zheng, Shiwei; Lazo, Suzan; Jardine, Laura; Dixon, David; Stephenson, Emily; Nilsson, Emil; Grundberg, Ida; McDonald, David; Filby, Andrew; Li, Weibo; De Jager, Philip L.; Rozenblatt-Rosen, Orit; Lane, Andrew A.; Haniffa, Muzlifah; Regev, Aviv; Hacohen, Nir (2017). "Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors". Science. 356 (6335): eaah4573. PMID 28428369. doi:10.1126/science.aah4573.
- Gierahn, Todd M; Wadsworth, Marc H; Hughes, Travis K; Bryson, Bryan D; Butler, Andrew; Satija, Rahul; Fortune, Sarah; Love, J Christopher; Shalek, Alex K (2017). "Seq-Well: Portable, low-cost RNA sequencing of single cells at high throughput". Nature Methods. 14 (4): 395–398. PMC 5376227 . PMID 28192419. doi:10.1038/nmeth.4179.
- Imielinski, Marcin; Rubin, Mark A. (2017). "Prostate cancer: Clinical hallmarks in whole cancer genomes". Nature Reviews Clinical Oncology. 14 (5): 265–266. PMID 28374788. doi:10.1038/nrclinonc.2017.45.
- Edelmann, J; Tausch, E; Landau, D A; Robrecht, S; Bahlo, J; Fischer, K; Fink, A M; Bloehdorn, J; Holzmann, K; Böttcher, S; Werner, L; Kneba, M; Gribben, J G; Neuberg, D S; Wu, C J; Hallek, M; Döhner, H; Stilgenbauer, S (2016). "Frequent evolution of copy number alterations in CLL following first-line treatment with FC(R) is enriched with TP53 alterations: Results from the CLL8 trial". Leukemia. 31 (3): 734–738. PMC 5332302 . PMID 27909343. doi:10.1038/leu.2016.317.
- Joung, Julia; Konermann, Silvana; Gootenberg, Jonathan S; Abudayyeh, Omar O; Platt, Randall J; Brigham, Mark D; Sanjana, Neville E; Zhang, Feng (2017). "Genome-scale CRISPR-Cas9 knockout and transcriptional activation screening". Nature Protocols. 12 (4): 828–863. PMID 28333914. doi:10.1038/nprot.2017.016.
- Curnin, Charles; Gordon, Assaf; Erlich, Yaniv (2017). "DNA Compass: A secure, client-side site for navigating personal genetic information". Bioinformatics. doi:10.1093/bioinformatics/btx135.
- Erlich, Yaniv; Zielinski, Dina (2017). "DNA Fountain enables a robust and efficient storage architecture". Science. 355 (6328): 950–954. Bibcode:2017Sci...355..950E. PMID 28254941. doi:10.1126/science.aaj2038.
- Khurana, Vikram; Peng, Jian; Chung, Chee Yeun; Auluck, Pavan K.; Fanning, Saranna; Tardiff, Daniel F.; Bartels, Theresa; Koeva, Martina; Eichhorn, Stephen W.; Benyamini, Hadar; Lou, Yali; Nutter-Upham, Andy; Baru, Valeriya; Freyzon, Yelena; Tuncbag, Nurcan; Costanzo, Michael; San Luis, Bryan-Joseph; Schöndorf, David C.; Barrasa, M. Inmaculada; Ehsani, Sepehr; Sanjana, Neville; Zhong, Quan; Gasser, Thomas; Bartel, David P.; Vidal, Marc; Deleidi, Michela; Boone, Charles; Fraenkel, Ernest; Berger, Bonnie; Lindquist, Susan (2017). "Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways". Cell Systems. 4 (2): 157–170.e14. PMC 5388136 . PMID 28131822. doi:10.1016/j.cels.2016.12.011.
- Manier, Salomon; Salem, Karma Z.; Park, Jihye; Landau, Dan A.; Getz, Gad; Ghobrial, Irene M. (2016). "Genomic complexity of multiple myeloma and its clinical implications". Nature Reviews Clinical Oncology. 14 (2): 100–113. PMID 27531699. doi:10.1038/nrclinonc.2016.122.
- Jønsson, K. L.; Laustsen, A.; Krapp, C.; Skipper, K. A.; Thavachelvam, K.; Hotter, D.; Egedal, J. H.; Kjolby, M.; Mohammadi, P.; Prabakaran, T.; Sørensen, L. K.; Sun, C.; Jensen, S. B.; Holm, C. K.; Lebbink, R. J.; Johannsen, M.; Nyegaard, M.; Mikkelsen, J. G.; Kirchhoff, F.; Paludan, S. R.; Jakobsen, M. R. (2017). "IFI16 is required for DNA sensing in human macrophages by promoting production and function of cGAMP". Nature Communications. 8: 14391. Bibcode:2017NatCo...814391J. PMC 5309897 . PMID 28186168. doi:10.1038/ncomms14391.
- Velasco, Silvia; Ibrahim, Mahmoud M.; Kakumanu, Akshay; Garipler, Görkem; Aydin, Begüm; Al-Sayegh, Mohamed Ahmed; Hirsekorn, Antje; Abdul-Rahman, Farah; Satija, Rahul; Ohler, Uwe; Mahony, Shaun; Mazzoni, Esteban O. (2017). "A Multi-step Transcriptional and Chromatin State Cascade Underlies Motor Neuron Programming from Embryonic Stem Cells". Cell Stem Cell. 20 (2): 205–217.e8. PMC 5291817 . PMID 27939218. doi:10.1016/j.stem.2016.11.006.
- MacIejowski, John; Imielinski, Marcin (2017). "Modeling cancer rearrangement landscapes". Current Opinion in Systems Biology. 1: 54–61. doi:10.1016/j.coisb.2016.12.005.
- Liu, Jimmy Z; Erlich, Yaniv; Pickrell, Joseph K (2017). "Case–control association mapping by proxy using family history of disease". Nature Genetics. 49 (3): 325–331. PMID 28092683. doi:10.1038/ng.3766.
- Imielinski, Marcin; Guo, Guangwu; Meyerson, Matthew (2017). "Insertions and Deletions Target Lineage-Defining Genes in Human Cancers". Cell. 168 (3): 460–472.e14. PMID 28089356. doi:10.1016/j.cell.2016.12.025.
- Fang, Han; Bergmann, Ewa A; Arora, Kanika; Vacic, Vladimir; Zody, Michael C; Iossifov, Ivan; O'Rawe, Jason A; Wu, Yiyang; Jimenez Barron, Laura T; Rosenbaum, Julie; Ronemus, Michael; Lee, Yoon-ha; Wang, Zihua; Dikoglu, Esra; Jobanputra, Vaidehi; Lyon, Gholson J; Wigler, Michael; Schatz, Michael C; Narzisi, Giuseppe (2016). "Indel variant analysis of short-read sequencing data with Scalpel". Nature Protocols. 11 (12): 2529–2548. PMID 27854363. doi:10.1038/nprot.2016.150.
References
- ↑ https://www.genomeweb.com/columns/people-news-cheryl-moore-hilde-windels-and-more%5B%5D
- ↑ http://www.nygenome.org/about-us/#our_members%5B%5D
- ↑ Duignan, Christopher (13 August 2015). "Form 990: Return of Organization Exempt From Income Tax" (PDF). GuideStar. p. 1. Retrieved 22 November 2016. (Registration required (help)).
- ↑ http://www.nygenome.org/wp-content/uploads/2017/04/AAG_Formatted.pdf%5B%5D
- 1 2 "New York Genome Center Launches Unprecedented Collaboration of 11 Leading Medical/Research Institutions". newsroom.cumc.columbia.edu. November 3, 2011. Retrieved 26 March 2017.
- ↑ "Tom Maniatis’ Dream of a NY Genome Center Becomes a Big Apple Reality". www.xconomy.com. Retrieved 26 March 2017.
- 1 2 3 "Robert Darnell named President of New York Genome Center". Rockefeller University Newswire. November 28, 2012. Retrieved 26 March 2017.
- ↑ Maher, Brendan (2013). "Biomedical-research hub opens in Manhattan". Nature. doi:10.1038/nature.2013.13740.
- ↑ Matheson, Sarah. "Genome Center Opens in New York". Epoch Times. Retrieved 26 March 2017.
- 1 2 3 4 5 6 7 8 9 Rosenthal, Eric T. (9 March 2016). "A New 'Manhattan Project': New York Genome Center". MedPage Today. Retrieved 21 November 2016.
- ↑ "Faculty". NYGC: About Us: Faculty. Retrieved 26 March 2017.
- ↑ "NIH News Release". NIH genome sequencing program targets the genomic bases of common, rare disease. Retrieved 26 March 2017.
- ↑ "Moving the New NY Forward (pdf)" (PDF). Retrieved 27 March 2017.
- 1 2 Di Mento, Maria (25 January 2016). "$100 Million for Genome Center and $75 Million for Hospital". Gifts Roundup. The Chronicle of Philanthropy. New York Genome Center. Retrieved 22 November 2016.
- 1 2 3 Lagasse, Jeff (21 January 2016). "New York Genome Center scores $100 million from James Simons, Russell Carson". Healthcare Finance. Retrieved 22 November 2016.
- ↑ "IBM’s Watson, New York Genome Center partner on brain cancer treatment". Washington Post. Retrieved 26 March 2017.
- ↑ Cha, Ariana. "IBM and New York Genome Center’s new cancer tumor repository aims to revolutionize treatment". www.washingtonpost.com. Retrieved 26 March 2017.
- ↑ "Einstein joins NYGC as 12th Founding Member". Retrieved 26 March 2017.
- ↑ Hargittai, István; Hargittai, Magdolna (2016). New York Scientific: A Culture of Inquiry, Knowledge, and Learning. Oxford, United Kingdom: Oxford University Press. p. 167. ISBN 9780191084683 – via Google Books.
- 1 2 "NY Genome Center Wins $13.5M from NHLBI Precision Medicine Program". GenomeWeb. 29 October 2015. Retrieved 22 November 2016. (Registration required (help)).
- ↑ "Weill Cornell Medicine and the New York Genome Center Awarded NCI Grant to Create Genomic Data Center". Bio-IT World. 3 November 2016. Retrieved 22 November 2016.
- 1 2 Cha, Ariana Eunjung (25 February 2016). "IBM and New York Genome Center’s new cancer tumor repository aims to revolutionize treatment". The Washington Post. Retrieved 21 November 2016.
- ↑ Herper, Matthew (19 March 2014). "IBM's Watson Attempts To Tackle The Genetics Of Brain Cancer". Forbes. Retrieved 22 November 2016.
- ↑ Jain, Kewal K. (2015). Textbook of Personalized Medicine (2nd ed.). Humana Press. ISBN 978-1-4939-2553-7. OCLC 900623470. doi:10.1007/978-1-4939-2553-7 – via Google Books.
- ↑ Ravindranath, Mohana (29 August 2014). "New Watson incarnation crunches academic literature". The Washington Post. Retrieved 22 November 2016.
- ↑ Wang, Baoying (2014). Big Data Analytics in Bioinformatics and Healthcare. Hershey, Pennsylvania: IGI Global. p. 423. ISBN 9781466666122. OCLC 890377536 – via Google Books.
- ↑ Reardon, Sara (2015). "Harold Varmus to resign as head of US cancer institute". Nature. doi:10.1038/nature.2015.17063.
- ↑ Sunkin-Strube, Alyssa (5 March 2015). "Nobel laureate Harold Varmus to join Weill Cornell April 1". Cornell Chronicle. Retrieved 22 November 2016.
- 1 2 "About Us". New York Genome. Retrieved 2016-12-21.