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use strict;
use warnings;
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use lib 't';
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use Test;
plan tests => 45;
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}
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use MultiTestDB;
use Bio::EnsEMBL::Slice;
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#
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#
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my $CHR = '20';
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my $END = 31_200_000;
my $STRAND = 1;
my $SEQ_REGION_LENGTH = 50e6;
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my $multi_db = MultiTestDB->new;
my $db = $multi_db->get_DBAdaptor('core');
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#
# TEST - Slice creation from adaptor
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#
my $slice_adaptor = $db->get_SliceAdaptor;
my $csa = $db->get_CoordSystemAdaptor();
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my $slice = $slice_adaptor->fetch_by_region('chromosome', $CHR, $START, $END);
ok($slice->seq_region_name eq $CHR);
ok($slice->start == $START);
ok($slice->end == $END);
ok($slice->seq_region_length == 62842997);
ok($slice->adaptor == $slice_adaptor);
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#
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#
my $coord_system = $csa->fetch_by_name('toplevel');
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$slice = new Bio::EnsEMBL::Slice
(-seq_region_name => $CHR,
-seq_region_length => $SEQ_REGION_LENGTH,
-start => $START,
-end => $END,
-strand => $STRAND,
-coord_system => $coord_system);
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ok($slice->seq_region_name eq $CHR);
ok($slice->start == $START);
ok($slice->end == $END);
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ok($slice->strand == $STRAND);
ok($slice->seq_region_length == $SEQ_REGION_LENGTH);
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#
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#
$slice->adaptor($slice_adaptor);
ok($slice->adaptor == $slice_adaptor);
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#
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#
#verify that chr_name start and end are contained in the name
my $name = $slice->name;
ok($name eq "chromosome:NCBI33:$CHR:$START:$END:$STRAND");
#
# Test Slice::length
#
ok($slice->length == ($END-$START + 1));
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#
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#
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my $clone = $slice_adaptor->fetch_by_region('clone','AL121583.25');
my @types = $clone->get_attribute_types();
ok(@types == 1 && $types[0] eq 'htg_phase');
my @attrib = $clone->get_attribute('htg_phase');
ok(@attrib == 1 && $attrib[0] == 4);
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#
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#
my $len = $clone->length();
$clone = $clone->expand(100,100);
ok(($clone->start == -99) && ($clone->end() == $len+100));
$clone = $clone->expand(-100,-100);
ok(($clone->start == 1) && ($clone->end() == $len));
$clone = $clone->expand(0,1000);
ok(($clone->start == 1) && ($clone->end() == $len + 1000));
$clone = $clone->expand(-1000, 0);
ok(($clone->start == 1001) && ($clone->end() == $len + 1000));
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#
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#
my $inverted_slice = $slice->invert;
ok($slice != $inverted_slice); #slice is not same object as inverted slice
#inverted slice on opposite strand
ok($slice->strand == ($inverted_slice->strand * -1));
#slice still on same strand
ok($slice->strand == $STRAND);
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#
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#
my $seq = uc $slice->seq;
my $invert_seq = uc $slice->invert->seq;
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ok(length($seq) == $slice->length); #sequence is correct length
$seq = reverse $seq; #reverse complement seq
$seq =~ tr/ACTG/TGAC/;
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ok($seq eq $invert_seq); #revcom same as seq on inverted slice
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#
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#
my $SPAN = 10;
my $sub_seq = uc $slice->subseq(-$SPAN,$SPAN);
my $invert_sub_seq = uc $slice->invert->subseq( $slice->length - $SPAN + 1,
$slice->length + $SPAN + 1);
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ok(length $sub_seq == (2*$SPAN) + 1 );
$sub_seq = reverse $sub_seq;
$sub_seq =~ tr/ACTG/TGAC/;
ok($sub_seq eq $invert_sub_seq);
#
# Test Slice::get_all_PredictionTranscripts
#
my $pts = $slice->get_all_PredictionTranscripts;
#
# Test Slice::get_seq_region_id
#
ok($slice->get_seq_region_id());
# Test Slice::get_all_DnaAlignFeatures
#
my $count = 0;
my $dafs = $slice->get_all_DnaAlignFeatures;
# Test Slice::get_all_ProteinAlignFeatures
#
my $pafs = $slice->get_all_ProteinAlignFeatures;
# Test Slice::get_all_SimilarityFeatures
#
ok($count == scalar @{$slice->get_all_SimilarityFeatures});
#
# Test Slice::get_all_SimpleFeatures
#
ok(scalar @{$slice->get_all_SimpleFeatures});
#
# Test Slice::get_all_RepeatFeatures
#
ok(scalar @{$slice->get_all_RepeatFeatures});
#
# Test Slice::get_all_Genes
#
ok(scalar @{$slice->get_all_Genes});
#
# Test Slice::get_all_Genes_by_type
#
ok(scalar @{$slice->get_all_Genes_by_type('ensembl')});
#
# Test Slice::get_all_KaryotypeBands
#
ok(scalar @{$slice->get_all_KaryotypeBands});
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# Test Slice::get_RepeatMaskedSeq
#
$seq = $slice->seq;
ok(length($slice->get_repeatmasked_seq->seq) == length($seq));
my $softmasked_seq = $slice->get_repeatmasked_seq(['RepeatMask'], 1)->seq;
ok($softmasked_seq ne $seq);
ok(uc($softmasked_seq) eq $seq);
$softmasked_seq = $seq = undef;
# Test Slice::get_all_MiscFeatures
ok(scalar @{$slice->get_all_MiscFeatures()});
ok(scalar @{$slice->project('seqlevel')});
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#my $super_slices = $slice->get_all_supercontig_Slices();
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##
## get_all_supercontig_Slices()
##
#debug( "Supercontig starts at ".$super_slices->[0]->chr_start() );
#ok( $super_slices->[0]->chr_start() == 29591966 );
#debug( "Supercontig name ".$super_slices->[0]->name() );
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#ok( $super_slices->[0]->name() eq "NT_028392" );
#
my $hash = $slice->get_base_count;
my $a = $hash->{'a'};
my $c = $hash->{'c'};
my $t = $hash->{'t'};
my $g = $hash->{'g'};
my $n = $hash->{'n'};
my $gc_content = $hash->{'%gc'};
debug( "Base count: a=$a c=$c t=$t g=$g n=$n \%gc=$gc_content");
ok($a == 234371
&& $c == 224761
&& $t == 243734
&& $g == 227135
&& $n == 0
&& $gc_content == 48.59
&& $a+$c+$t+$g+$n == $slice->length);
my $test_seq = 'ATGCATGCATGCATGCATGCATGC';
my $test_slice = new Bio::EnsEMBL::Slice
(-seq_region_name => 'misc',
-seq_region_length => 24,
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-start => 1,
-end => 24,
-strand => 1,
-coord_system => $coord_system,
-seq => $test_seq,
);
ok($test_slice->length == 24);
$hash = $test_slice->get_base_count;
$a = $hash->{'a'};
$c = $hash->{'c'};
$t = $hash->{'t'};
$g = $hash->{'g'};
$n = $hash->{'n'};
$gc_content = $hash->{'%gc'};
ok($a == 6
&& $c == 6
&& $t == 6
&& $g == 6
&& $n == 0
&& $gc_content == 50
&& $a+$c+$t+$g+$n == $test_slice->length);