Difference between revisions of "Website:Data Structure (old page)"

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(New page: I'm keeping this around so I don't always have to look in the code! This page will document the contents of the data structure of the new site. Each section describes the returning dat...)
 
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Latest revision as of 17:11, 4 May 2010

I'm keeping this around so I don't always have to look in the code!


This page will document the contents of the data structure of the new site. Each section describes the returning data structure for a method.


Gene

Overview

ids()

description => "Data for gene WBGeneID"
data =>
common_name => scalar
locus_name => scalar
version => scalar
aceview_id => scalar
refseq_id => scalar
other_names => array
sequence_names => array

public_name()

description => ""
data => scalar

common_name()

description => ""
data => scalar

concise_description()

description => "A manually curated description of the gene's function"
data =>
<WBGeneID> => scalar

gene_models()

description => "gene model summary for the gene"
data =>

... no data pack?

history()

description => ""
data =>
<History Object ID> =>
<Version Object ID> =>
type => scalar
date => scalar
action => scalar
remark => scalar
curator => scalar

Sequences

spliced()

unspliced()

translated()

Variation

Overview

name()

description => "The object name of the variation"
data => scalar

common_name()

description => "The public name of the variation"
data => scalar

cgc_name()

description => "The Caenorhabditis Genetics Center (CGC) name for the gene"
data => scalar

other_names()

description => "other possible names for the variation"
data => array

variation_type()

description => "the general type of the variation"
data => scalar

remarks()

description => "curator remarks for the variation"
data => array

Molecular Details

type_of_mutation()

description => "the type of mutation and its molecular change"
data => scalar

nucleotide_change()

description => "raw nucleotide changes for this variation"
data => scalar

flanking_sequences()

description => "probes used for CGH of deletion alleles"
data =>
left_flank => scalar
right_flank => scalar

cgh_deleted_probes()

description => "probes used for CGH of deletion alleles"
data =>
left_flank => scalar
right_flank => scalar

context()

description => "wildtype and mutant sequences in an expanded genomic context"
data =>
wildtype_fragment => scalar
wildtype_full => scalar
mutant_fragment => scalar
mutant_full => scalar
wildtype_header => "> Wild type N2, with 250 bp flanks<br>wildtype_full",
mutant_header => "> $object with 250 bp flanks<br>mutant_full"

deletion_verification()

description => "the type of mutation and its molecular change"
data => scalar

features_affected()

description => "the method used to verify deletion alleles"
data =>
Pseudogene=>
<entry>=>
Transcript=>
Predicted_CDS=>
Gene=>
Clone=>
Chromosome=>

flanking_pcr_products()

description => "genomic features affected by this variation"
data => scalar

Protein