Skip to content
Snippets Groups Projects
Commit b6ec8723 authored by Graham McVicker's avatar Graham McVicker
Browse files

fixed some deprecated b/w compatibility methods which were broken due to...

fixed some deprecated b/w compatibility methods which were broken due to changed toplevel definition
parent 1e27829e
No related branches found
No related tags found
No related merge requests found
......@@ -477,11 +477,11 @@ sub get_seq_region_attribs {
Arg [2] : string $coord_system_version (optional)
The version of the coordinate system to retrieve slices of
Arg [3] : bool $include_non_reference (optional)
If this argument is not provided then onlt reference slices
will be returned. If set both reference and non refeference
slices will be rerurned.
If this argument is not provided then only reference slices
will be returned. If set, both reference and non refeference
slices will be rerurned.
Arg [4] : int $no_duplicates (optional)
If set eno duplicate entries will be returned.
If set no duplicate entries will be returned.
Example : @chromos = @{$slice_adaptor->fetch_all('chromosome','NCBI33')};
@contigs = @{$slice_adaptor->fetch_all('contig')};
......@@ -494,8 +494,12 @@ sub get_seq_region_attribs {
seq_regions and are on the forward strand.
If the coordinate system with the provided name and version
does not exist an empty list is returned.
If the coordinate system name provided is 'toplevel', all
If the coordinate system name provided is 'toplevel', all
non-redundant toplevel slices are returned.
Retrieved slices can be broken into smaller slices using the
Bio::EnsEMBL::Utils::Slice module.
Returntype : listref of Bio::EnsEMBL::Slices
Exceptions : none
Caller : general
......@@ -519,7 +523,6 @@ sub fetch_all {
my $sth;
my %bad_vals=();
#
# Get a hash of non reference seq regions
......@@ -571,45 +574,47 @@ sub fetch_all {
while($sth->fetch()) {
if(!defined($bad_vals{$seq_region_id})){
my $cs = $csa->fetch_by_dbID($cs_id);
if(!$cs) {
throw("seq_region $name references non-existent coord_system $cs_id.");
throw("seq_region $name references non-existent coord_system $cs_id.");
}
my $cs_key = lc($cs->name().':'.$cs_version);
#cache values for future reference, but stop adding to the cache once we
#we know we have filled it up
if($cache_count < $SEQ_REGION_CACHE_SIZE) {
my $key = lc($name) . ':'. $cs_key;
$name_cache->{$key} = [$seq_region_id, $length];
$id_cache->{$seq_region_id} = [$name, $length, $cs];
$cache_count++;
my $key = lc($name) . ':'. $cs_key;
$name_cache->{$key} = [$seq_region_id, $length];
$id_cache->{$seq_region_id} = [$name, $length, $cs];
$cache_count++;
}
my $slice = Bio::EnsEMBL::Slice->new(-START => 1,
-END => $length,
-STRAND => 1,
-SEQ_REGION_NAME => $name,
-SEQ_REGION_LENGTH => $length,
-COORD_SYSTEM => $cs,
-ADAPTOR => $self);
if(!defined($include_duplicates) or !$include_duplicates){ #do not include duplicates
my @dup = @{$self->fetch_normalized_slice_projection($slice)};
foreach my $dup_test( @dup){
if($dup_test->[2]->get_seq_region_id == $slice->get_seq_region_id){
push @out, $dup_test->[2];
}
}
my $slice = Bio::EnsEMBL::Slice->new
(-START => 1,
-END => $length,
-STRAND => 1,
-SEQ_REGION_NAME => $name,
-SEQ_REGION_LENGTH => $length,
-COORD_SYSTEM => $cs,
-ADAPTOR => $self);
if(!defined($include_duplicates) or !$include_duplicates){
#do not include duplicates
my @dup = @{$self->fetch_normalized_slice_projection($slice)};
foreach my $dup_test( @dup){
if($dup_test->[2]->get_seq_region_id == $slice->get_seq_region_id){
push @out, $dup_test->[2];
}
}
}
else{
push @out, $slice;
else {
push @out, $slice;
}
}
}
$sth->finish();
return \@out;
}
......@@ -1281,7 +1286,7 @@ sub fetch_by_chr_start_end {
#assume that by chromosome the user actually meant top-level coord
#system since this is the old behaviour of this deprecated method
my $csa = $self->db->get_CoordSystemAdaptor();
my $cs = $csa->fetch_top_level();
my ($cs) = @{$csa->fetch_all()}; # get the highest coord system
return $self->fetch_by_region($cs->name,$chr,$start,$end,1,$cs->version);
}
......@@ -1303,20 +1308,18 @@ sub fetch_by_contig_name {
#previously wanted chromosomal slice on a given contig. Assume this means
#a top-level slice on a given seq_region in the seq_level coord system
my $csa = $self->db()->get_CoordSystemAdaptor();
my $top_level = $csa->fetch_top_level();
my $seq_level = $csa->fetch_sequence_level();
my $seq_lvl_slice = $self->fetch_by_region($seq_level->name(), $name);
my @projection = @{$seq_lvl_slice->project($top_level->name(),
$top_level->version())};
if(@projection == 0) {
warning("contig $name is not used in ".$top_level->name().' assembly.');
if(!$seq_lvl_slice) {
return undef;
}
if(@projection > 1) {
warning("$name is mapped to multiple locations in " . $top_level->name());
my @projection = @{$seq_lvl_slice->project('toplevel')};
if(@projection != 1) {
warning("$name is mapped to multiple toplevel locations.");
}
return $projection[0]->[2]->expand($size, $size);
......@@ -1336,7 +1339,6 @@ sub fetch_by_clone_accession{
deprecate('Use fetch_by_region(), Slice::project() and Slice::expand().');
my $csa = $self->db()->get_CoordSystemAdaptor();
my $top_level = $csa->fetch_top_level();
my $clone_cs = $csa->fetch_by_name('clone');
if(!$clone_cs) {
......@@ -1363,15 +1365,12 @@ sub fetch_by_clone_accession{
}
my $clone = $self->fetch_by_region($clone_cs->name(), $name);
my @projection = @{$clone->project($top_level->name(),
$top_level->version())};
if(@projection == 0) {
warning("clone $name is not used in " . $top_level->name() . ' assembly.');
return undef;
}
return undef if(!$clone);
if(@projection > 1) {
warning("$name is mapped to multiple locations in " . $top_level->name());
my @projection = @{$clone->project('toplevel')};
if(@projection != 1) {
warning("$name is mapped to multiple locations.");
}
return $projection[0]->[2]->expand($size, $size);
......@@ -1391,7 +1390,6 @@ sub fetch_by_supercontig_name {
deprecate('Use fetch_by_region(), Slice::project() and Slice::expand().');
my $csa = $self->db()->get_CoordSystemAdaptor();
my $top_level = $csa->fetch_top_level();
my $sc_level = $csa->fetch_by_name('supercontig');
if(!$sc_level) {
......@@ -1401,16 +1399,12 @@ sub fetch_by_supercontig_name {
my $sc_slice = $self->fetch_by_region($sc_level->name(),$name);
my @projection = @{$sc_slice->project($top_level->name(),
$top_level->version())};
if(@projection == 0) {
warning("Supercontig $name is not used in " . $top_level->name() .
' assembly.');
return undef;
}
return undef if(!$sc_slice);
my @projection = @{$sc_slice->project('toplevel')};
if(@projection > 1) {
warning("$name is mapped to multiple locations in " . $top_level->name());
warning("$name is mapped to multiple locations in toplevel");
}
return $projection[0]->[2]->expand($size, $size);
......@@ -1431,7 +1425,6 @@ sub list_overlapping_supercontigs {
deprecate('Use Slice::project() instead.');
my $csa = $self->db()->get_CoordSystemAdaptor();
my $top_level = $csa->fetch_top_level();
my $sc_level = $csa->fetch_by_name('supercontig');
if(!$sc_level) {
......
......@@ -114,11 +114,11 @@ sub ctg2genomic{
my $top_level = $csa->fetch_top_level();
my $ma = $aa->fetch_by_CoordSystems($top_level, $self->coord_system);
return $ma->map_coordinates_to_assembly( $self->seq_region_name,
$start,
$end,
$strand,
$self->coord_system);
return $ma->map( $self->seq_region_name,
$start,
$end,
$strand,
$self->coord_system);
}
......
0% or .
You are about to add 0 people to the discussion. Proceed with caution.
Finish editing this message first!
Please register or to comment