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A user that has a patient's informed consent to analyze the clinical data may upload sequence variants to GeneTalk in variant call format (VCF) (Danecek et al., 2011), version 4.0 and above.
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Alternatively, users may upload homologous sequences of their own.
The institute's agreements with these countries included permission to upload sequences to publicly accessible repositories.
The user interface allows the user to upload sequences both as zipped batches and as individual uploads.
It is also time-consuming to upload sequencing data and reference sequences.
Users can upload sequences to share with others or use privately.
Users may upload their own molecules to the TCM database server in mol2 format.
Users may upload their BLAST outputs (Altschul et al., 1997) to the server to view the alignments between the query and the subject sequences.
Users may upload their own genomes together with lineage information.
You may upload a BAM file in exactly the same manner as you uploaded a SAM file.
In addition, one may upload a custom (undirected) network, which may be weighted.
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