funder-graph

FundersWASage Bionetworks › 2020

Grants paid by Sage Bionetworks, tax year 2020

EIN 26-4489946 · Seattle, WA · Form 990, Schedule I · NTEE U50

In tax year 2020, Sage Bionetworks (EIN 26-4489946) reported 8 grants paid totaling $1,462,461. Dataset version 2026.09.0, built 2026-09-03.

20182020202220232024

Every grant, 2020

Grants reported by Sage Bionetworks for tax year 2020
Tax yearRecipientMatchAmountTypePurposeSource filing
2020Institute for Systems Biology Seattle, WAA$436,242paidA data and analytic platform for immuno-oncology community.202113139349303681
2020Icahn School of Medicine at Mount Sinai New York, NYA$317,805paidInterdisciplinary Research to Understand the Complex Biology of Resilience to Alzheimer's Disease Risk is to generate deeper understanding of the mechanisms by which gene environment interactions lead to cognitively resilient phenotypes in the presence of high risk for disease and identify new therapeutic targets amenable to pharmacologic and non-pharmacologic disease prevention strategies.202113139349303681
2020University of Washington Seattle, WAA$214,468paidWellcome is engaging the Supplier as a learning partner to prototype and test best ways to build a Global Mental Health Databank (GMH Databank) that holds rich longitudinal data at scale from different global locations on approaches, treatments and interventions potentially relevant to anxiety or depression in 14- 24 year olds in order to help answer the question: "what works for whom and why in relation to prevention, treatment, stopping relapse or managing ongoing difficulties for anxiety or depression including at least some 14-24 year olds" (the "Global Mental Health Databank" or "GMH Databank").202113139349303681
2020Boston University New York, NYA$186,548paidAccelerating alzheimer's disease innovation and discovery by lowering barriers to Framingham cognitive aging and dementia data.202113139349303681
2020University of Arizona Tucson, AZA$142,840paidThe goal of the project is to validate small molecules (from in silico docking on the CD44 binding pocket and peptidomimetics of CD44 peptide) and peptides (from the peptide array) to disrupt the interaction between CD44 and FERM domain-containing proteins. These tools will further test the druggability of CD44 interactions with Moesin, and whether targeting protein-protein interactions can have a more specific effects than global inhibition of the ectodomain of CD44 using antibodies or small molecules. This will pave the way to validating therapeutic hypotheses for AMP-AD targets relating to protein-protein interactions.202113139349303681
2020Oregon Health & Science University Portland, ORA$75,086paidExisting computational methods for single-cell RNA-seq signal correction and single-cell ATAC-seq peak quantification will be evaluated to select baseline methods respectively for each task, for comparison in the competition. An evaluation criteria will be developed for universal assessment of the participating computational approaches using public and in-house data. Additional experimental data for further validation will be generated and used, including dual experimental assay of scRNA-seq and scATAC-seq. Final results of the community challenge will be disseminated in multiple ways, including scientific manuscript.202113139349303681
2020Tufts University Boston, MAA$53,548paidDr. Williams will oversee the project and be responsible for the acquisition, mapping, and transfer of Tuft MC data to N3C, and for its use in a proof-of-concept analysis. He will work with Dr Justin Guinney and the leads of the N3C workstreams for Data Partnerships and Governance, Phenotype and Data Acquisition, and Data Ingestion and Harmonization, and the Palantir platform team (in-kind support only) to implement N3C policies and practices for data governance, transfer, ingestion, storage, and use. He will be a stakeholder collaborator to the "Core Team" of developers. Dr. Williams will also promote the contribution of high-resolution ICU data from other sites to N3C using the mappings from the ETL and disseminate resources that educate N3C users how signal analytic tools can be productively applied to these data.202113139349303681
2020Ibm Yorktown Heights, NYA$35,924paidAdvancing benchmarking and data sharing through crowd-sourced data competitions in cancer research and management.202113139349303681

Match tier: A Reported EIN · B Exact name and place · C Strong name match · D Probable name match · U Unresolved. Tiers C and D are inferred, not reported; see how matching works.

Recipient matching for this dataset version has not yet completed its independent precision check. Tier A rows carry the EIN the filer reported; tiers B–D are the matcher's inference and should be read as leads until the check is published on the methodology page.

Derived from IRS Form 990 e-file XML. Dataset version 2026.09.0, built 2026-09-03. All years for this funder.

The same organization elsewhere in the program: exempt status and filing health · federal awards · grant guidance · open opportunities.

This is informational only, derived from public data on the dates shown. It is not an eligibility determination, and not legal, tax, or accounting advice. Verify against the official source before relying on it.