Difference between revisions of "WormBase Model:Multi pt data"
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== Model == | == Model == | ||
<pre> | <pre> | ||
+ | ?Multi_pt_data Evidence #Evidence | ||
+ | Genotype UNIQUE Text | ||
+ | Experiment Mapper ?Author | ||
+ | Laboratory ?Laboratory | ||
+ | Date UNIQUE DateType | ||
+ | Selected A UNIQUE Gene_A UNIQUE ?Gene UNIQUE ?Variation XREF In_multi_point | ||
+ | Locus_A UNIQUE ?Locus UNIQUE ?Variation XREF In_multi_point | ||
+ | Allele_A UNIQUE ?Variation | ||
+ | Rearrangement_A UNIQUE ?Rearrangement | ||
+ | Transgene_A UNIQUE ?Transgene XREF Multi_point | ||
+ | B UNIQUE Gene_B UNIQUE ?Gene UNIQUE ?Variation XREF In_multi_point | ||
+ | Locus_B UNIQUE ?Locus UNIQUE ?Variation XREF In_multi_point | ||
+ | Allele_B UNIQUE ?Variation | ||
+ | Rearrangement_B UNIQUE ?Rearrangement | ||
+ | Transgene_B UNIQUE ?Transgene XREF Multi_point | ||
+ | Gene ?Gene UNIQUE ?Variation XREF In_multi_point // Connect to ?Gene model | ||
+ | Locus ?Locus UNIQUE ?Variation XREF In_multi_point // Pair up alleles | ||
+ | Results A_non_B #Multi_counts | ||
+ | B_non_A #Multi_counts | ||
+ | Combined #Multi_counts | ||
+ | Old_CGC_results Text | ||
+ | Remark ?Text #Evidence | ||
+ | // code uses all the Results subtags, and the #Multi_counts structure | ||
</pre> | </pre> | ||
== Proposed Changes == | == Proposed Changes == | ||
+ | |||
+ | == Unused tags== | ||
+ | |||
+ | Transgene_A | ||
+ | |||
+ | Transgene_B |
Latest revision as of 15:52, 4 October 2010
Curator Comments/Description
Model
?Multi_pt_data Evidence #Evidence Genotype UNIQUE Text Experiment Mapper ?Author Laboratory ?Laboratory Date UNIQUE DateType Selected A UNIQUE Gene_A UNIQUE ?Gene UNIQUE ?Variation XREF In_multi_point Locus_A UNIQUE ?Locus UNIQUE ?Variation XREF In_multi_point Allele_A UNIQUE ?Variation Rearrangement_A UNIQUE ?Rearrangement Transgene_A UNIQUE ?Transgene XREF Multi_point B UNIQUE Gene_B UNIQUE ?Gene UNIQUE ?Variation XREF In_multi_point Locus_B UNIQUE ?Locus UNIQUE ?Variation XREF In_multi_point Allele_B UNIQUE ?Variation Rearrangement_B UNIQUE ?Rearrangement Transgene_B UNIQUE ?Transgene XREF Multi_point Gene ?Gene UNIQUE ?Variation XREF In_multi_point // Connect to ?Gene model Locus ?Locus UNIQUE ?Variation XREF In_multi_point // Pair up alleles Results A_non_B #Multi_counts B_non_A #Multi_counts Combined #Multi_counts Old_CGC_results Text Remark ?Text #Evidence // code uses all the Results subtags, and the #Multi_counts structure
Proposed Changes
Unused tags
Transgene_A
Transgene_B