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From the home screen, click on any project to which you have UPLOAD, CONTRIBUTE, or ADMIN access, then click Add Data. Follow instructions in the Add Data dialog.
ua sample_1_left.fastq.gz sample_1_right.fastq.gz
Your MiSeq instrument produces run results in the folder
D:\Illumina\MiSeqOutputor on a network path that you specify. After on-instrument secondary analysis is complete, the reads are available in
*.fastq.gzfiles in the subfolder
/Data/Intensities/BaseCalls/of the run folder. For example, the first file may be called
Visit the European Nucleotide Archive (ENA) and locate there your SRA dataset (sequencing run) of choice. For example, if you search for "SRR001662", you will reach the result page for sequencing run SRR001662. On that page, the "Read Files" panel contains FTP links to fastq files (under the "Fastq files (ftp)" column). To import these reads, in your project click "Add Data", choose "Transfer from another server" and supply these links.
If the track has an associated BED, GTF, or WIG file, use the link to that file as input to the URL Fetcher app (platform login required). This app will launch a job that will download the file and upload it to your DNAnexus project.
For example, the default UCSC Genome Browser view for hg19 includes a track called "Digital DNaseI Hypersensitivity Clusters from ENCODE". If you click on the gray rectangle to the left of the track to configure it, you will find a "downloads" link that leads you to a gzipped BED file with the track data. The link to that file can given as the input to the URL Fetcher app (platform login required).
Not all UCSC Genome Browser tracks include links to downloadable data. However, you can still export most tracks into BED using the UCSC "Table Browser". Select "Table Browser" from the "Tools" menu at the top, and choose the track of interest. In the "output format" select BED, and type in a filename. Click the "Get Output" button to download a BED file.