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      1. Carlos Slim Center for Health Research The Slim Center aims to bring the benefits of genomics-driven medicine to Latin America, gleaning new insights into diseases with relevance to the region.
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      3. Klarman Cell Observatory The Klarman Cell Observatory is systematically defining mammalian cellular circuits, how they work together to create tissues and organs, and are perturbed to cause disease.
      4. Merkin Institute for Transformative Technologies in Healthcare The Merkin Institute is supporting early-stage ideas aimed at advancing powerful technological approaches for improving how we understand and treat disease.
      5. Novo Nordisk Foundation Center for Genomic Mechanisms of Disease This center is developing new paradigms and technologies to scale the discovery of biological mechanisms of common, complex diseases, by facilitating close collaborations between the Ó³»­´«Ã½ and the Danish research community.
      6. Eric and Wendy Schmidt Center The EWSC is catalyzing a new field of interdisciplinary research at the intersection of data science and life science, aimed at improving human health.
      7. Stanley Center for Psychiatric Research The Stanley Center aims to reduce the burden of serious mental illness by contributing new insights into pathogenesis, identifying biomarkers, and paving the way toward new treatments.
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      1. Art and science connection Explore the connection between art and science and how we bring together artists and Ó³»­´«Ã½ scientists through our artist-in-residence program, gallery exhibitions, and ongoing public conversations.
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Cohesin mutations and chromatin changes in cancer.
Swett AD, Tothova Z. Cohesin mutations and chromatin changes in cancer. International journal of cancer. 2025. doi:10.1002/ijc.35378
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Refining the cis-regulatory grammar learned by sequence-to-activity models by increasing model resolution.
Chandra NA, Hu Y, Buenrostro JD, Mostafavi S, Sasse A. Refining the cis-regulatory grammar learned by sequence-to-activity models by increasing model resolution. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.01.24.634804
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Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
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Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
Read more
Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
Read more
Increased nuclear factor I-mediated chromatin access drives transition to androgen receptor splice variant dependence in prostate cancer.
Poluben L, Nouri M, Liang J, et al. Increased nuclear factor I-mediated chromatin access drives transition to androgen receptor splice variant dependence in prostate cancer. Cell reports. 2024;44(1):115089. doi:10.1016/j.celrep.2024.115089
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A high-throughput synthetic biology approach for studying combinatorial chromatin-based transcriptional regulation.
Alcantar MA, English MA, Valeri JA, Collins JJ. A high-throughput synthetic biology approach for studying combinatorial chromatin-based transcriptional regulation. Molecular cell. 2024;84(12):2382-2396.e9. doi:10.1016/j.molcel.2024.05.025
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Dissection of a CTCF topological boundary uncovers principles of enhancer-oncogene regulation.
Kim KL, Rahme GJ, Goel VY, Farran CAE, Hansen AS, Bernstein BE. Dissection of a CTCF topological boundary uncovers principles of enhancer-oncogene regulation. Molecular cell. 2024. doi:10.1016/j.molcel.2024.02.007
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A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.
Singh AK, Allington G, Viviano S, et al. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus. Brain : a journal of neurology. 2023. doi:10.1093/brain/awad405
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Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction.
Shi X, Lu C, Corman A, et al. Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction. American journal of human genetics. 2023;110(10):1750-1768. doi:10.1016/j.ajhg.2023.09.004
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In March of 2020, Ó³»­´«Ã½ converted a clinical genetics processing lab into a large-scale COVID-19 testing facility in less than two weeks.

We've screened more than 1,275 cancer cell lines as part of the Cancer Dependency Map (DepMap).

Ó³»­´«Ã½ Genomics Platform sequences a whole human genome every four minutes.

More than 11,000 individuals living with cancer in the United States and Canada have partnered with Count Me In to share their experiences and help accelerate cancer research.

The Drug Repurposing Hub is one of the most comprehensive and up-to-date biologically annotated collections of FDA-approved compounds in the world. Researchers anywhere can explore more than 6,000 drugs in the hub and search for possible new uses for them to jump-start new drug discovery.

In 2021, our sustainability efforts sent more than 80 percent of waste from the Genomics Platform to either a recycling facility or to an incineration plant that generates electricity.

Through Ó³»­´«Ã½'s Scientists in the Classroom program, Ó³»­´«Ã½ researchers visit every 8th grade classroom in Cambridge each year to talk about genetics and evolution.

Every summer, 18 high school students spend six weeks at Ó³»­´«Ã½ working side-by-side with mentors on cutting-edge research.

In November 2022, Ó³»­´«Ã½â€™s Genomics Platform sequenced its 500,000th whole human genome, a mere four years after sequencing its 100,000th.

By the end of 2022, Ó³»­´«Ã½â€™s COVID-19 testing lab had processed more than 37 million tests.

Working with Addgene, Ó³»­´«Ã½ has shared CRISPR genome-editing reagents with researchers at more than 3,200 institutions in 76 countries.

The NeuroGAP-Psychosis project, a collaboration between the Stanley Center for Psychiatric Research and Harvard T.H. Chan School of Public Health to study the genetics of severe mental illness, has recruited more than 42,000 participants in Ethiopia, Kenya, Uganda, and South Africa.

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