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Copy file name to clipboardExpand all lines: Model/config/datasetLinks.xml
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<?xml version="1.0" encoding="UTF-8"?>
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<links>
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<linktype="genome"subtype="null">
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<linkcategory="Genomes">
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<text>View the DEFAULT_PROJECT Genomic Sequence Page for an Example Sequence</text>
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<description><![CDATA[
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The Genomic Sequence Page is a view of a chromosome, contig, or scaffold. We provide summary information, a link to the Genome Browser, and a form for sequence retrieval. All Genomic Sequence Searches return this type of record.
<text>View a partial region of an Example Sequence in the DEFAULT_PROJECT Genome Browser</text>
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<description><![CDATA[
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Each Sequence for this dataset can be browsed using the Genome Browser. Here we provide a sample region with tracks which are available for all sequences.
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</link>
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<!-- TODO: replace this link with a link to the dataset record for this organism -->
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<linktype="genome"subtype="null">
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<linkcategory="Genomes">
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<text>View the DEFAULT_PROJECT Organism Record Page</text>
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<description><![CDATA[
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The Organism Record page contains a summary of the different types of data associated with this organism. How many genes? Does this organism have RNA Sequence Data? ...
<text>Run BLAST on sequences in DEFAULT_PROJECT</text>
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<description><![CDATA[
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BLAST finds regions of similarity between sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. VEuPathDB BLAST accommodates inputs such as a single sequence or several FASTA-formatted sequences at once, i.e., is multi-query capable.
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<linktype="est"subtype="null">
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<linkcategory="EST">
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<text>Run BLAST on sequences in DEFAULT_PROJECT</text>
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<description><![CDATA[
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BLAST finds regions of similarity between sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. VEuPathDB BLAST accommodates inputs such as a single sequence or several FASTA-formatted sequences at once, i.e., is multi-query capable.
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<linktype="protein_expression"subtype="null">
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<linkcategory="Protein expression">
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<text>View peptides aligned to an Example Protein in the DEFAULT_PROJECT Genome Browser</text>
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<description><![CDATA[
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<linktype="protein_expression"subtype="null">
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<linkcategory="Protein expression">
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<text>View peptides aligned to an Example Protein in the DEFAULT_PROJECT Protein Browser</text>
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<description><![CDATA[
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</link>
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<linktype="protein_expression"subtype="null">
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<linkcategory="Protein expression">
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<text>View the DEFAULT_PROJECT Proteomics Section on an Example Gene Page</text>
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<description><![CDATA[
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Copy file name to clipboardExpand all lines: Model/lib/wdk/model/questions/params/geneParams.xml
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select distinct 'long_transcript_novelty' as ontology_term_name, cast(null as varchar(1)) as parent_ontology_term_name,
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'Support From Long Read Evidence' as display_name, 'Find genes based on overlapping models from long read RNA sequencing, for example from Oxford Nanopore or PacBio sequencing platforms. To be considered in this query, a model must have at least 5 supporting reads and be at least 20 bases long. Categories as follows: Novel in Collection (NIC): Prediction uses known splice donors and acceptors but reveals new connections (e.g., skipped exon isoforms); Incomplete Splice Match (ISM): Prediction matches subsection of a known transcript model, but has a novel putative start or end point; Novel Not In Collection (NNC): Prediction has at least one novel splice donor or acceptor; Genomic: Prediction has no overlapping splice junctions compared to known transcripts; Genomic: Prediction has no overlapping splice junctions compared to known transcripts; Known: Prediction exactly matches a known model. NOTE: The percentage add up to more than 100% because one existing gene model can have more than associated TALON model.' as description, cast(null as varchar(1)) as units,
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'string' as type, 0 as is_range, cast(null as varchar(1)) as precision, 7 as display_order
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from apidbtuning.datasetnametaxon dnt
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from apidbtuning.datasetdatasource dd
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where '$$gene_or_transcript$$' = 'gene_source_id'
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and dnt.name like '%nanopore_longReadRnaSeq_RSRC'
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and dnt.taxon_id in ($$organism_select_all$$)
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and dd.name like '%nanopore_longReadRnaSeq_RSRC'
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and dd.taxon_id in ($$organism_select_all$$)
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and '@PROJECT_ID@' != 'EuPathDB'
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UNION
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select 'intron_junction' as ontology_term_name, cast(null as varchar(1)) as parent_ontology_term_name,
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Copy file name to clipboardExpand all lines: Model/lib/wdk/model/records/geneAttributeQueries.xml
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SELECT ga.source_id, ga.project_id, v.annotation_version as ds_annotation_version, v.dataset_presenter_id as dataset_id, v.description as attribution_partial
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