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Query Data
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NDAR provides a single access to de-identified autism research data. For permission to download data, you will need an NDAR account
with approved access to NDAR or a connected repository (AGRE, IAN, or the ATP). For NDAR access, you need to be a research
investigator sponsored by an NIH recognized institution with federal wide assurance.
See Request Access for more information.
Warning Notice
This is a U.S. Government computer system, which may be accessed and used only for authorized Government business by authorized personnel. Unauthorized access or use of this computer system may subject violators to criminal, civil, and/or administrative action.
All information on this computer system may be intercepted, recorded, read, copied, and disclosed by and to authorized personnel for official purposes, including criminal investigations. Such information includes sensitive data encrypted to comply with confidentiality and privacy requirements. Access or use of this computer system by any person, whether authorized or unauthorized, constitutes consent to these terms. There is no right of privacy in this system.
For projects that share genomic or proteomic results, published and provided alterations are available for query using NDAR's omicSEARCH.
To use this feature, search by alteration type (e.g. SNP, CNV, SNV), affected region, chromosome, cytoband, etc., returning specific alterations.
Selected alterations can then be applied -- via Show Results -- against participant data, including phenotypic categories and imaging results in NDAR.
Authenticated users will be able to search by significance values and download participant data.
How to use this dialog
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Enter your search criteria in the input fields. Most fields will take a comma-separated list of values. The system will suggest values as you type.
To see all available values before typing, press the up or down arrow key. You may navigate through the suggestion list with the mouse or keyboard.
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Once you have entered all values you wish to search by, click the "Show Results" button on the bottom of the dialog. This will populate the table
with all alterations that match your criteria. You can use the table navigation controls to select how many alterations to see at a time and to navigate
forward, back, or to a specific page of alterations.
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Check the "Select" box next to all alterations you would like to see subjects for, then click the "Apply" button at the bottom of the dialog. The
dialog will close and the main page will display the subjects that match your selected alterations, including selection criteria for phenotype,
imaging, and basic demographics.