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Weight tracker template tri fold3/28/2024 What are Association Analysis Data Files and how should they be formatted? How do I link individual study subjects/samples to samples that have been submitted to NCBI databases: GEO, GenBank, SRA (public)? How do I submit Copy Number Variation (CNV) data? How do I submit High Throughput Sequence data and alignment information? What should I know about editing, proofreading, and copyright? What type of Study Documents may I submit and in what format? How do I verify that my DS and DD Files will pass dbGaP's phenotype quality control (QC) tests? How do I submit Medical Images and in what format? How do I create Sample Attributes DS and DD files? How do I create Subject Phenotypes DS and DD files? What data must be included in the Subject Phenotypes and Sample Attributes? How do I create Pedigree DS and DD files? How do I create Subject Sample Mapping (SSM) DS and DD files? How do I create Subject Consent (SC) DS and DD files? What is a Phenotype Data Dictionary (DD) File? What do I need to know about protecting study participants' privacy, HIPAA, and subject de-identification for dbGaP data submissions? Where can I download dbGaP Submission Guide Templates to generate the files I need to submit? Use the questions below to jump to relevant sections or use your browser's find function to search for keywords. A new Subject Sample Telemetry Report (SSTR) webpage and API are available to search and filter on study level Subject and Sample IDs, consents, summary counts, processing status, and molecular and sequence sample uses.For more information, please see the glossary entry " Collections". To search for dbGaP Collections, visit Advanced Search. One Data Access Request (DAR) will provide you with the ability to request for all the studies within a dbGaP Collection at once. A dbGaP Collection includes studies or portions of studies that share the same consent group, disease, or funding project. We now have 12 dbGaP Collections with more in progress.An enhanced dbGaP Advanced Search is now available for users to filter for third-party annotations of Common Data Elements, dbGaP Collections, sensitivity designations of Genomic Summary Results (GSR), and studies with External Data Sources (EDS).Review "How to Submit" -> Register study -> Prepare files for submission -> Check files before submission -> Submit -> dbGaP curators process -> Receive signal and submit high throughput sequences: BAM, CRAM, FASTQ -> Preview and Approve -> Release Submission Onboarding DbGaP Study Submission Guide You must register your study before submitting data.
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