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The open access data in the NF Data Portal is generated by studies backed by funding organizations, including Children’s Tumor Foundation (CTF), Neurofibromatosis Therapeutic Acceleration Program (NTAP), and Gilbert Family Foundation (GFF). Some studies are funded in conjunction with one another—such a group of funded projects is called an initiative on the portal. Funded studies produce data files, metadata (also called and annotations), publications, and biological tools like cell lines, mouse models, and plasmids. Study products, such as multiple data files, may be bundled into a dataset, or explored and analyzed with computational tools developed by the community.
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The NF Data Portal was built by members of the NF Open Science Initiative (NF-OSI), an alliance that was formed to support open science within the neurofibromatosis and schwannomatosis research community. NF-OSI is the result of a collaboration effort between the Children’s Tumor Foundation (CTF) and the Neurofibromatosis therapeutic acceleration program Therapeutic Acceleration Program (NTAP) that dates back to 2014 (you can read more about these programs here). This is an open effort focusing on finding NF treatments by sharing data and analysis results with the broader community—an effort aided by the existence of the NF Data Portal.
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Sage Bionetworks | First, there’s Sage Bionetworks - a name you may or may not have come across. While Sage is not a tool you’ll be using, you should know what it is—the company behind all of this! We are a non-profit organization based out of Seattle, Washington. Sage is dedicated to promoting and advancing open science, as well as engaging patients in the research process. Sage acts as the Data Coordinating Center (DCC) for several different portals, including the NF Data Portal. The scientists, developers, and designers that built the tools you’re using are all employed by Sage. You can learn more about Sage Bionetworks and its initiatives here. |
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Synapse | In line with advocating for open science, Sage developed a software platform called Synapse. This platform is what allows fo for collaborative data curation and analysis, computational modelling, and more. It allows users to upload, store, analyze, and tack your track data in a private space, before releasing it to the public-facing NF Data Portal. Think if of Synapse as the back-end for all the data to live in. |
NF Data Portal | If Synapse is the back-end for data, the NF Data Portal is the front. It’s essentially the user interface (UI) or entry point for you to view data and other shared content. Data gets uploaded into Synapse, where it is then processed into readable form for you to access in the portal. |
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Data standards underpin data sharing and make it possible to successfully explore, access, analyze, and reuse data. Data standards involve:
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The majority of data available in the NF Data Portal is sequencing data, such as RNA sequencing and whole exome sequencing, though we also have a variety of imaging assays and other data. We derive most of our data standards , and collection of standardized keys and values from vetted sources such as the National Cancer Institute’s Genomic Data Commons (NCI’s GDC) and NCI Thesaurus. If you already use or consult those standards, many of NF’s standards will be familiar to you.
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The items associated with those keys (such as assay, platform, studyID) are called values, and would appear in within the cells of a spreadsheet cells.
To allow for data standards, we control the terminology used for values through (meta)data dictionaries and other tools. Using controlled vocabularies and other data standards allows you to find what you’re looking for on the portal, so that you don’t have to search through multiple terms for the same thing. For example, instead of ribonucleic acid sequencing, or RNA-Seq, we use the value rnaSeq.
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