BioPerl-DB
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sql/markerdb-mysql.sql view on Meta::CPAN
common_name varchar(64) not null
);
-- constraint: only two strains should be associated with a single map study!
-- (at least for terrestrial organisms)
CREATE TABLE strain_to_map_study (
strain_id integer(11) not null,
map_study_id integer(11) not null,
UNIQUE (strain_id,map_study_id)
);
CREATE TABLE map (
map_id integer(11) not null AUTO_INCREMENT PRIMARY KEY,
map_study_id integer(11) not null,
map_name varchar(32) not null,
linkage_group varchar(32), -- ???? or chromosome?
UNIQUE (map_study_id,map_name)
);
-- This is essential the locus table, in which markers are assigned to maps
-- with a position. To accomodate QTLs, position may be a range.
-- There is no constraint that a single marker must map to a single position
-- on a map or a map study.
-- Unfortunately, markers sometimes do map to several places on the same map!
CREATE TABLE map_position (
map_position_id integer(11) not null AUTO_INCREMENT PRIMARY KEY,
marker_id integer(11) not null,
map_id integer(11) not null,
position_start float(8,4) not null, -- unresolved question: what about markers that
position_stop float(8,4), -- are assigned to chromosome but not to positions?
KEY i_marker_map (marker_id,map_id),
KEY i_position (map_id,position_start,position_stop)
);
CREATE TABLE marker (
marker_id integer(11) not null AUTO_INCREMENT PRIMARY KEY,
marker_table varchar(32),
evidence_id integer(11)
);
CREATE TABLE marker_to_dna (
marker_id integer(11) not null,
dna_id integer(11) not null, -- this is the Ensembl dna.id key
KEY i_marker_dna (marker_id,dna_id)
);
CREATE TABLE marker_rflp (
marker_id integer(11) not null PRIMARY KEY,
enzyme_id integer(11) not null
);
CREATE TABLE marker_rapd (
marker_id integer(11) not null PRIMARY KEY,
oligo_id integer(11) not null
);
CREATE TABLE marker_microsatellite (
marker_id integer(11) not null PRIMARY KEY,
oligo1_id integer(11) not null,
oligo2_id integer(11) not null,
flanking_gc_percent float(8,4),
length_low integer(6),
length_high integer(6),
motif varchar(128) not null
);
CREATE TABLE marker_sts (
marker_id integer(11) not null PRIMARY KEY,
oligo1_id integer(11) not null,
oligo2_id integer(11) not null
);
CREATE TABLE marker_morphological (
marker_id integer(11) not null PRIMARY KEY,
trait_id integer(11) not null -- coming from the Trait Ontology
);
CREATE TABLE marker_aflp (
marker_id integer(11) not null PRIMARY KEY,
oligo1_id integer(11) not null,
oligo2_id integer(11) not null,
cycle_count integer(11), -- same as "amplification" in RiceGenes
molecular_weight float(8,4)
);
CREATE TABLE marker_isozyme (
marker_id integer(11) not null PRIMARY KEY,
go_id integer(11) not null, -- from the Gene Ontology (tm)
molecular_weight float(8,4)
);
create table marker_alias (
marker_id integer(11) not null,
alias varchar(64) not null,
evidence_id integer(11) not null,
UNIQUE (marker_id,alias)
);
CREATE TABLE enzyme (
enzyme_id integer(11) not null AUTO_INCREMENT PRIMARY KEY,
enzyme_name varchar(64) not null
);
CREATE TABLE next_number (
table_name varchar(64) not null PRIMARY KEY,
next_number integer(11) not null
);
------------------------ Marker Equivalence Table ---------------------
CREATE TABLE marker_to_marker_group (
marker_group_id integer(11) not null,
marker_id integer(11) not null,
UNIQUE (marker_group_id,marker_id)
);
CREATE TABLE marker_group (
marker_group_id integer(11) not null AUTO_INCREMENT PRIMARY KEY,
evidence_id integer(11) not null
);
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