def testSubcomponent(self):
self.assertEquals(self.testees[0].subcomponent, None)
uri = random_uri()
self.uris.append(uri)
com = sbol.DNAComponent(self.doc, uri)
self.testees[0].subcomponent = com
self.assertEquals(self.testees[0].subcomponent, com)
def initialize_design(doc):
n_designs = len([part for part in doc.components if part.type and part.type == DESIGN])
root = sbol.DNAComponent(doc, '%s/Design_%d' %(BASE_URI, n_designs + 1))
root.type = DESIGN
root.display_id = 'Design %d' %(n_designs + 1)
root.name = 'Design %d' %(n_designs + 1)
root.sequence = sbol.DNASequence(doc, '%s/Design_%d/Seq_%d' %(BASE_URI, n_designs + 1, n_designs + 1))
root.sequence.nucleotides = 'n'
return root
def testComponents(self):
col = self.testees[0]
for n in range(NUM_SLOW_TESTS):
self.assertEqual(len(col.components), n)
uri = random_uri()
self.uris.append(uri)
com = sbol.DNAComponent(self.doc, uri)
self.assertFalse(com in col.components)
col.components += com
self.assertTrue(com in col.components)
self.assertEqual(len(col.components), n + 1)
def sbol(self):
doc = sbol.Document()
dc = sbol.DNAComponent(doc, "#" + str(self.pk) + "_con")
dc.display_id = str(self.name)
dc.description = str(self.description)
dc.sequence = sbol.DNASequence(doc, "#" + str(self.pk) + "_seq")
dc.sequence.nucleotides = str(self.sequence())
fid = [1]
l = self.length()
def makeAnnot(f, parent=dc):
if self.shape == 'c' and f.end > l and parent == dc:
end = f.end
f.end = l
makeAnnot(f, parent)
f.end = end - l
f.start = 0
makeAnnot(f, parent)
return
dcf = sbol.DNAComponent(doc, "#dc_" + str(fid[0]))
dcf.display_id = str(f.type)
dcf.description = str(";".join(["%s:%s" % (q.name,q.data) for q in f.qualifiers.all()]))
sa = sbol.SequenceAnnotation(doc, "#sa_" + str(fid[0]))
sa.subcomponent = dcf
if f.direction == 'f':
sa.strand = '+'
else:
sa.strand = '-'
sa.start = f.start + 1 # SBOL 1-based
sa.end = f.end + 1
parent.annotations.append(sa)
fid[0] += 1
return dcf
fragments = {}
fragmentfeats = {}
for f in self.features(False): # sub-annotations relative to parent
try:
if f.gene is not None:
if f.type == "fragment":
fragments[f.gene] = f
else:
if f.gene in fragmentfeats:
fragmentfeats[f.gene].append(f)
else:
fragmentfeats[f.gene] = [f]
except:
makeAnnot(f)
for gene, fragment in fragments.iteritems():
dcf = makeAnnot(fragment)
dcf.description = str(gene.description)
if gene in fragmentfeats:
for f in fragmentfeats[gene]:
makeAnnot(f, dcf)
return str(doc)
def makeAnnot(f, parent=dc):
if self.shape == 'c' and f.end > l and parent == dc:
end = f.end
f.end = l
makeAnnot(f, parent)
f.end = end - l
f.start = 0
makeAnnot(f, parent)
return
dcf = sbol.DNAComponent(doc, "#dc_" + str(fid[0]))
dcf.display_id = str(f.type)
dcf.description = str(";".join(["%s:%s" % (q.name,q.data) for q in f.qualifiers.all()]))
sa = sbol.SequenceAnnotation(doc, "#sa_" + str(fid[0]))
sa.subcomponent = dcf
if f.direction == 'f':
sa.strand = '+'
else:
sa.strand = '-'
sa.start = f.start + 1 # SBOL 1-based
sa.end = f.end + 1
parent.annotations.append(sa)
fid[0] += 1
return dcf
def qc(design, data=None, infile=None):
if infile:
with open(infile, "r") as f:
data = f.read()
if data:
if len(parse_fasta(data)) > 1:
multialignment = align(data)
clone = find_consensus(multialignment)
else:
clone = data
target_design = write_to_fasta([(design.uri,
design.sequence.nucleotides)])
alignment_qc = align(target_design + '\r\n' + clone,
outfile='%s.align' % design.display_id)
# Scan alignment and classify mutations
design_seq = design.sequence.nucleotides
reference_seq = parse_fasta(alignment_qc)[0][1][:]
query_seq = parse_fasta(alignment_qc)[1][1][:]
assert len(reference_seq) == len(query_seq)
# Translate alignment coordinates into coordinates of the reference and query sequences
l_alignment = len(reference_seq) # Determine length of alignment
l_ref = len(reference_seq.replace('-', ''))
l_que = len(query_seq.replace('-', ''))
# The following dictionaries are used like lists indexed from one
ref_map = {
} # Maps nucleotide coordinates of reference sequence to alignment coordinates
i_ref = 0
# If the design sequence is not fully covered by sequencing data, there may be '---' padding the end of
# the query sequence. The following indices mark the padded regions of the query_seq
# Eg,
# ref actggtca
# qry --tggt--
#
i_left = query_seq.index(
next(token for token in query_seq if not token == '-'))
i_right = len(query_seq) - query_seq[::-1].index(
next(token for token in reversed(query_seq) if not token == '-'))
for i_alignment in range(l_alignment):
ref_base = reference_seq[i_alignment]
que_base = query_seq[i_alignment]
if not ref_base == '-':
i_ref += 1
# Do not map the design coordinates to alignment coordinates if they aren't covered
if i_alignment >= i_left and i_alignment <= i_right:
ref_map[i_ref] = i_alignment
# Should be a unit test
#for i in range(0, l_ref):
# assert design_sequence[i] == reference_seq[ref_map[i+1]], "%d %s does not match %s"%(i,design_sequence[i], reference_seq[ref_map[i+1]])
# Only leaf annotations at the bottom of the hierarchy are annotated...
leaf_annotations = []
for i_design in range(len(design_seq)):
target_annotations = getSequenceAnnotationsAtBaseNo(
design, i_design)
for ann in target_annotations:
if not ann in leaf_annotations:
leaf_annotations.append(ann)
# Slice the alignment into segments that pertain to each annotation,
# then determine the covered bases in the annotation. All, part, or several discontiguous parts of an annotation
# may be covered
for i_ann, ann in enumerate(leaf_annotations):
covered_coordinates = list(
ref_map.keys()
) # List of all base coordinates for this design / reference sequence that are covered
# Now narrow down to find just the bases in this annotation
covered_coordinates = [
x for x in covered_coordinates
if x >= ann.start and x <= ann.end
]
# Now translate into alignment coordinates
alignment_coordinates = [ref_map[x] for x in covered_coordinates]
if len(alignment_coordinates) > 0:
alignment_start = min(alignment_coordinates)
alignment_end = max(alignment_coordinates)
# Scan alignment
print("Verifying %s from %d to %d" %
(ann.subcomponent.display_id, ann.start, ann.end))
print(''.join([
nt for nt in reference_seq[alignment_start:alignment_end]
]))
print(''.join(
[nt for nt in query_seq[alignment_start:alignment_end]]))
# Classification of alignment
base_comparisons = [
verify_base(reference_seq[x], query_seq[x])
for x in alignment_coordinates
]
for x in alignment_coordinates:
comparison = verify_base(reference_seq[x], query_seq[x])
if comparison == None:
print(x, reference_seq[x], query_seq[x])
# Select a contiguous region of interest in alignment coordinates
# TODO: replace while with for
i_alignment = 0
regions = []
region_classifications = []
while i_alignment < len(base_comparisons):
current_term = base_comparisons[i_alignment]
if i_alignment == 0:
reg_start = 0
reg_end = 0
previous_term = None
elif i_alignment > 0 and i_alignment < (
len(base_comparisons) - 1):
# Mark end of an old region of interest and beginning of a new region
if not current_term == previous_term:
ref_start = covered_coordinates[
reg_start] # Translate from alignment to design / reference coordinates
ref_end = covered_coordinates[
reg_end] # Translate from alignment to design / reference coordinates
region_of_interest = ((ref_start, ref_end),
previous_term)
regions.append(region_of_interest)
reg_start = i_alignment
reg_end = i_alignment
# Else extend the old region of interest to include the current coordinate
elif current_term == previous_term:
reg_end = i_alignment
elif i_alignment == (len(base_comparisons) - 1):
if not current_term == previous_term:
reg_start = i_alignment
reg_end = i_alignment
ref_start = covered_coordinates[
reg_start] # Translate from alignment to design / reference coordinates
ref_end = covered_coordinates[
reg_end] # Translate from alignment to design / reference coordinates
region_of_interest = ((ref_start, ref_end),
previous_term)
regions.append(region_of_interest)
elif current_term == previous_term:
reg_end = i_alignment
ref_start = covered_coordinates[
reg_start] # Translate from alignment to design / reference coordinates
ref_end = covered_coordinates[
reg_end] # Translate from alignment to design / reference coordinates
region_of_interest = ((ref_start, ref_end),
previous_term)
regions.append(region_of_interest)
#print i_alignment, current_term, reg_start, reg_end, covered_coordinates[reg_start], covered_coordinates[reg_end]
previous_term = current_term
i_alignment += 1
# TODO: add unit test checking that the first region starts and the last region ends
# TODO: add unit test checking that two distinct regions of interest can be demarcated
# TODO: add unit test checking a single base region of interest at the beginning or the start
# TODO: add unit test checking if first or last bases of query are '-'. These are currently classified as
# insertions, but are in fact uncovered regions
# Create SequenceAnnotations for QC'd regions
doc = design.doc
for i_region, region in enumerate(regions):
print(i_region)
qc_start, qc_end = region[0]
qc_classification = region[1]
n_components = len(doc.components)
n_annotations = len(doc.annotations)
if qc_classification:
if qc_classification == SO_NUCLEOTIDE_MATCH: # The reference sequence matches the query sequence
annotated_region = sbol.SequenceAnnotation(
doc, "%s/MatchedSequence/SA%d" %
(design.uri, n_annotations))
annotated_region.start = qc_start
annotated_region.end = qc_end
annotated_region.subcomponent = sbol.DNAComponent(
doc, "%s/MatchedSequence/SA%d/DC%d" %
(design.uri, n_annotations, n_components))
annotated_region.subcomponent.display_id = ""
annotated_region.subcomponent.type = qc_classification
else: # A mismatch was identified
annotated_region = sbol.SequenceAnnotation(
doc, "%s/AssemblyErrors/SA%d" %
(design.uri, n_annotations))
annotated_region.start = qc_start
annotated_region.end = qc_end
annotated_region.subcomponent = sbol.DNAComponent(
doc, "%s/AssemblyErrors/SA%d/DC%d" %
(design.uri, n_annotations, n_components))
annotated_region.subcomponent.display_id = ""
annotated_region.subcomponent.type = qc_classification
print("Adding %s to %s from %d to %d" %
(annotated_region.uri, ann.subcomponent.display_id,
annotated_region.start, annotated_region.end))
ann.subcomponent.annotations.append(annotated_region)
def createTestees(self):
uri = random_uri()
self.uris.append(uri)
self.testees.append(sbol.DNAComponent(self.doc, uri))
