def draw_breakpoint(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
breakpoint: Breakpoint,
width: int,
height: int,
label: str = '',
) -> svgwrite.container.Group:
"""
Args:
canvas: the main svgwrite object used to create new svg elements
breakpoint: the breakpoint to draw
width: the pixel width
height: the pixel height
Return:
the group element for the diagram
"""
g = canvas.g(class_='breakpoint')
y = config.padding + config.breakpoint_label_font_size / 2
t = canvas.text(
label,
insert=(width / 2, y + config.font_central_shift_ratio *
config.breakpoint_label_font_size),
fill=HEX_BLACK,
style=config.font_style.format(
text_anchor='middle', font_size=config.breakpoint_label_font_size),
class_='label',
)
y += config.breakpoint_label_font_size / 2 + config.padding
g.add(t)
r = canvas.rect((0, y), (width, height - y),
stroke=config.breakpoint_color,
fill='none')
r.dasharray(config.breakpoint_stroke_dasharray)
g.add(r)
if breakpoint.orient == ORIENT.LEFT:
line = canvas.line((0, y), (0, height))
line.stroke(config.breakpoint_color,
width=config.breakpoint_orient_stroke_width)
g.add(line)
elif breakpoint.orient == ORIENT.RIGHT:
line = canvas.line((width, y), (width, height))
line.stroke(config.breakpoint_color,
width=config.breakpoint_orient_stroke_width)
g.add(line)
g.add(
Tag(
'title',
'Breakpoint {}:g.{}_{}{} {}'.format(
breakpoint.chr,
breakpoint.start,
breakpoint.end,
breakpoint.strand,
breakpoint.orient,
),
))
return g
def draw_vmarker(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
marker: 'BioInterval',
width: int,
height: int,
label='',
color=None,
) -> svgwrite.container.Group:
"""
Args:
canvas: the main svgwrite object used to create new svg elements
width: the pixel width
height: the pixel height
Return:
the group element for the diagram
"""
color = config.marker_color if color is None else color
g = canvas.g(class_='marker')
y = config.padding + config.marker_label_font_size / 2
t = canvas.text(
label,
insert=(
width / 2, y +
config.font_central_shift_ratio * config.marker_label_font_size),
fill=color,
style=config.font_style.format(
text_anchor='middle', font_size=config.marker_label_font_size),
class_='label',
)
y += config.marker_label_font_size / 2 + config.padding
g.add(t)
g.add(canvas.rect((0, y), (width, height - y), stroke=color, fill='none'))
g.add(
Tag(
'title',
'marker {}:{}-{} {}'.format(marker.reference_object, marker.start,
marker.end, marker.name),
))
return g
def draw_template(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
template,
target_width,
labels=None,
colors=None,
breakpoints=None,
) -> svgwrite.container.Group:
"""
Creates the template/chromosome illustration
Return:
the group element for the diagram
"""
labels = LabelMapping() if labels is None else labels
colors = {} if colors is None else colors
breakpoints = [] if not breakpoints else breakpoints
total_height = (config.template_track_height +
config.breakpoint_top_margin +
config.breakpoint_bottom_margin)
group = canvas.g(class_='template')
# 1 as input since we don't want to change the ratio here
mapping = generate_interval_mapping(
template.bands,
target_width,
1,
config.template_band_min_width,
start=template.start,
end=template.end,
)
scaffold = canvas.rect((0, 0), (target_width, config.scaffold_height),
fill=config.scaffold_color)
group.add(scaffold)
scaffold.translate((
0,
config.breakpoint_top_margin + config.template_track_height / 2 -
config.scaffold_height / 2,
))
label_group = canvas.g()
label_group.add(
canvas.text(
labels.add(template, config.template_label_prefix),
insert=(
0 - config.padding,
config.breakpoint_top_margin +
config.template_track_height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=config.label_color,
style=config.font_style.format(font_size=config.label_font_size,
text_anchor='end'),
class_='label',
))
label_group.add(Tag('title', 'template {}'.format(template.name)))
group.add(label_group)
for band in template.bands:
s = mapping.convert_pos(band[0])
t = mapping.convert_pos(band[1])
bgroup = canvas.g(class_='cytoband')
f = config.template_band_fill.get(band.data.get('giemsa_stain', None),
config.template_default_fill)
r = None
w = t - s + 1
if band.data.get('giemsa_stain', None) == GIEMSA_STAIN.ACEN:
if band.name[0] == 'p':
r = canvas.polyline(
[
(0, 0),
(w, config.template_track_height / 2),
(0, config.template_track_height),
],
fill=f,
stroke=config.template_band_stroke,
stroke_width=config.template_band_stroke_width,
)
else:
r = canvas.polyline(
[
(w, 0),
(0, config.template_track_height / 2),
(w, config.template_track_height),
],
fill=f,
stroke=config.template_band_stroke,
stroke_width=config.template_band_stroke_width,
)
else:
r = canvas.rect(
(0, 0),
(w, config.template_track_height),
fill=f,
stroke=config.template_band_stroke,
stroke_width=config.template_band_stroke_width,
)
bgroup.add(r)
bgroup.add(
Tag(
'title',
'cytoband {0}:y.{1} {0}:g.{2}_{3}'.format(
template.name, band.name, band.start, band.end),
))
bgroup.translate((s, config.breakpoint_top_margin))
group.add(bgroup)
# now draw the breakpoints overtop
for i, b in enumerate(sorted(breakpoints)):
s = mapping.convert_pos(b.start)
t = mapping.convert_pos(b.end)
bg = draw_breakpoint(
config,
canvas,
b,
abs(t - s) + 1,
total_height,
label=labels.add(b, config.breakpoint_label_prefix),
)
bg.translate(s, 0)
group.add(bg)
setattr(group, 'height', total_height)
return group
def draw_exon_track(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
transcript,
mapping: IntervalMapping,
colors=None,
genomic_min: int = None,
genomic_max: int = None,
translation=None,
) -> svgwrite.container.Group:
""" """
colors = {} if colors is None else colors
main_group = canvas.g(class_='exon_track')
y = config.track_height / 2
exons = sorted(transcript.exons, key=lambda x: x.start)
exonic_min = min([e.start for e in exons])
exonic_max = max([e.end for e in exons])
genomic_min = exonic_min if genomic_min is None else min(
genomic_min, exonic_min)
genomic_max = exonic_max if genomic_max is None else max(
genomic_max, exonic_max)
start = mapping.convert_ratioed_pos(exonic_min)
start = start.start if exonic_min == genomic_min else start.end
end = mapping.convert_ratioed_pos(exonic_max)
end = end.end if exonic_max == genomic_max else end.start
main_group.add(
canvas.rect(
(start, y - config.scaffold_height / 2),
(end - start + 1, config.scaffold_height),
fill=config.scaffold_color,
class_='scaffold',
))
# draw the exons
for i, exon in enumerate(exons):
start = mapping.convert_ratioed_pos(exon.start)
end = mapping.convert_ratioed_pos(exon.end)
if exon.start == genomic_min or (i > 0
and exon.start - exons[i - 1].end == 1
): # consecutive with previous exon
start = start.start
else:
start = start.end
if exon.end == genomic_max or (i < len(exons) - 1
and exons[i + 1].start - exon.end == 1
): # consecutive with following exon
end = end.end
else:
end = end.start
pxi = Interval(*sorted(
[start,
end])) # for very small intervals (single bp) these may reverse
try:
exon_number = transcript.exon_number(exon)
except KeyError:
exon_number = 'n'
exon_height = config.track_height
if len(exon) < config.exon_min_focus_size:
if exon_number == 'n':
exon_height = config.track_height + config.ins_increase
exon_number = '' # don't add labels to very small exons
exon_width = max(config.non_focus_min_width, pxi.length())
group = draw_exon(
config,
canvas,
exon,
exon_width,
exon_height,
colors.get(exon, config.exon1_color),
label=exon_number,
translation=translation,
)
group.translate(pxi.center - exon_width / 2, y - exon_height / 2)
main_group.add(group)
setattr(main_group, 'height', y + config.track_height / 2)
setattr(main_group, 'width', end - start + 1)
return main_group
def draw_exon(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
exon: 'Exon',
width: int,
height: int,
fill: str,
label: str = '',
translation=None,
) -> svgwrite.container.Group:
"""
generates the svg object representing an exon
Args:
canvas: the main svgwrite object used to create new svg elements
exon (Exon): the exon to draw
width: the pixel width
height: the pixel height
fill: the fill color to use for the exon
Return:
the group element for the diagram
Todo:
add markers for exons with abrogated splice sites
"""
g = canvas.g(class_='exon')
label = str(label)
g.add(canvas.rect((0, 0), (width, height), fill=fill))
t = canvas.text(
label,
insert=(width / 2, height / 2 +
config.font_central_shift_ratio * config.exon_font_size),
fill=config.label_color
if not config.dynamic_labels else dynamic_label_color(fill),
style=config.font_style.format(font_size=config.exon_font_size,
text_anchor='middle'),
class_='label',
)
g.add(t)
title = 'Exon {} g.{}_{}'.format(exon.name if exon.name else '',
exon.start, exon.end)
if translation:
cds_start = translation.convert_genomic_to_cds_notation(exon.start)
cds_end = translation.convert_genomic_to_cds_notation(exon.end)
if exon.get_strand() == STRAND.NEG:
cds_start, cds_end = cds_end, cds_start
title += ' c.{}_{}'.format(cds_start, cds_end)
try:
cdna_start = translation.transcript.convert_genomic_to_cdna(
exon.start)
cdna_end = translation.transcript.convert_genomic_to_cdna(exon.end)
if cdna_end < cdna_start:
cdna_start, cdna_end = cdna_end, cdna_start
title += ' cdna({}_{})'.format(cdna_start, cdna_end)
except IndexError:
title += ' cdna(N/A)'
title += ' length({})'.format(len(exon))
if exon.seq and len(exon.seq) < config.exon_min_focus_size:
title += ' seq={}'.format(exon.seq)
g.add(Tag('title', title))
return g
def draw_genes(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
genes: List['Gene'],
target_width: int,
breakpoints: Optional[List[Breakpoint]] = None,
colors: Optional[Dict[str, 'Gene']] = None,
labels: Optional[LabelMapping] = None,
plots: Optional[List] = None,
masks: Optional[List[Interval]] = None,
) -> svgwrite.container.Group:
"""
draws the genes given in order of their start position trying to minimize
the number of tracks required to avoid overlap
Args:
canvas: the main svgwrite object used to create new svg elements
target_width: the target width of the diagram
genes: the list of genes to draw
breakpoints: the breakpoints to overlay
colors: dictionary of the colors assigned to each Gene as fill
Return:
the group element for the diagram. Has the added parameters of labels, height, and mapping
"""
# mutable default argument parameters
breakpoints = [] if breakpoints is None else breakpoints
colors = {} if colors is None else colors
labels = LabelMapping() if labels is None else labels
plots = plots if plots else []
st = max(
min([g.start for g in genes] + [b.start for b in breakpoints]) -
config.gene_min_buffer, 1)
end = max([g.end for g in genes] +
[b.end for b in breakpoints]) + config.gene_min_buffer
main_group = canvas.g(class_='genes')
mapping = generate_interval_mapping(
[g for g in genes],
target_width,
config.gene_intergenic_ratio,
config.gene_min_width,
start=st,
end=end,
min_inter_width=config.min_width,
)
if masks is None:
masks = []
try:
if len(breakpoints) == 1:
b = breakpoints[0]
if b.orient == ORIENT.RIGHT:
masks = [Interval(st, b.start - 1)]
elif b.orient == ORIENT.LEFT:
masks = [Interval(b.end + 1, end)]
elif len(breakpoints) == 2:
b1, b2 = sorted(breakpoints)
if b1.orient == ORIENT.LEFT and b2.orient == ORIENT.RIGHT:
masks = [Interval(b1.end, b2.start)]
except AttributeError:
pass
gene_px_intervals = {}
for i, gene in enumerate(sorted(genes, key=lambda x: x.start)):
s = mapping.convert_ratioed_pos(gene.start)
t = mapping.convert_ratioed_pos(gene.end)
gene_px_intervals[Interval(s.start, t.end)] = gene
labels.add(gene, config.gene_label_prefix)
tracks = split_intervals_into_tracks(gene_px_intervals)
y = config.breakpoint_top_margin
main_group.add(
canvas.rect(
(
0,
y + config.track_height / 2 - config.scaffold_height / 2 +
(len(tracks) - 1) * (config.track_height + config.padding),
),
(target_width, config.scaffold_height),
fill=config.scaffold_color,
class_='scaffold',
))
tracks.reverse()
for track in tracks: # svg works from top down
for genepx in track:
# draw the gene
gene = gene_px_intervals[genepx]
group = draw_gene(
config,
canvas,
gene,
genepx.length(),
config.track_height,
colors.get(gene, config.gene1_color),
labels.get_key(gene),
)
group.translate(genepx.start, y)
main_group.add(group)
y += config.track_height + config.padding
y += config.breakpoint_bottom_margin - config.padding
# adding the masks is the final step
for mask in masks:
pixel = mapping.convert_ratioed_pos(
mask.start) | mapping.convert_ratioed_pos(mask.end)
m = canvas.rect(
(pixel.start, 0),
(pixel.length(), y),
class_='mask',
fill=config.mask_fill,
pointer_events='none',
opacity=config.mask_opacity,
)
main_group.add(m)
# now overlay the breakpoints on top of everything
for i, b in enumerate(sorted(breakpoints)):
s = mapping.convert_ratioed_pos(b.start).start
t = mapping.convert_ratioed_pos(b.end).end
bg = draw_breakpoint(
config,
canvas,
b,
abs(t - s) + 1,
y,
label=labels.add(b, config.breakpoint_label_prefix),
)
bg.translate(s, 0)
main_group.add(bg)
setattr(main_group, 'height', y)
setattr(main_group, 'width', target_width)
setattr(main_group, 'mapping', mapping)
setattr(main_group, 'labels', labels)
return main_group
def draw_ustranscript(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
pre_transcript,
target_width: Optional[int] = None,
breakpoints: List['Breakpoint'] = [],
labels=LabelMapping(),
colors={},
mapping=None,
masks=None,
reference_genome=None,
) -> svgwrite.container.Group:
"""
builds an svg group representing the transcript. Exons are drawn in a track with the splicing
information and domains are drawn in separate tracks below
if there are multiple splicing variants then multiple exon tracks are drawn
Args:
canvas: the main svgwrite object used to create new svg elements
target_width: the target width of the diagram
pre_transcript (Transcript): the transcript being drawn
breakpoints: the breakpoints to overlay
Return:
the group element for the transcript diagram Has the added parameters of labels, height, and mapping
"""
if pre_transcript.get_strand() not in [STRAND.POS, STRAND.NEG]:
raise NotSpecifiedError(
'strand must be positive or negative to draw the pre_transcript')
if (mapping is None
and target_width is None) or (mapping is not None
and target_width is not None):
raise AttributeError(
'mapping and target_width arguments are required and mutually exclusive'
)
genomic_min = min([e.start
for e in pre_transcript.exons] + [pre_transcript.start])
genomic_max = max([e.end
for e in pre_transcript.exons] + [pre_transcript.end])
if mapping is None:
try:
exons_to_map = [
e for e in pre_transcript.exons
if len(e) >= config.exon_min_focus_size
]
except AttributeError:
exons_to_map = pre_transcript.exons
mapping = generate_interval_mapping(
exons_to_map,
target_width,
config.exon_intron_ratio,
config.exon_min_width,
min_inter_width=config.min_width,
start=genomic_min,
end=genomic_max,
)
main_group = canvas.g(class_='pre_transcript')
y = config.breakpoint_top_margin if len(breakpoints) > 0 else 0
if masks is None:
masks = []
try:
if len(breakpoints) == 1:
b = breakpoints[0]
if b.orient == ORIENT.RIGHT:
masks = [Interval(pre_transcript.start, b.start - 1)]
elif b.orient == ORIENT.LEFT:
masks = [Interval(b.end + 1, pre_transcript.end)]
elif len(breakpoints) == 2:
b1, b2 = sorted(breakpoints)
if b1.orient == ORIENT.LEFT and b2.orient == ORIENT.RIGHT:
masks = [Interval(b1.end + 1, b2.start - 1)]
except AttributeError:
pass
label_prefix = config.transcript_label_prefix
if isinstance(pre_transcript, FusionTranscript):
label_prefix = config.fusion_label_prefix
if not pre_transcript.translations:
y += config.splice_height
exon_track_group = draw_exon_track(config, canvas, pre_transcript,
mapping, colors)
exon_track_group.translate(0, y)
exon_track_group.add(
canvas.text(
labels.add(pre_transcript, label_prefix),
insert=(
0 - config.padding,
config.track_height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=config.label_color,
style=config.font_style.format(
font_size=config.label_font_size, text_anchor='end'),
class_='label',
))
exon_track_group.add(
Tag(
'title', 'Transcript: {}'.format(
pre_transcript.name if pre_transcript.name else '')))
main_group.add(exon_track_group)
y += config.track_height
else:
# draw the protein features if there are any
for i, tl in enumerate(pre_transcript.translations):
gp = draw_transcript_with_translation(
config,
canvas,
tl,
labels,
colors,
mapping,
genomic_min=genomic_min,
genomic_max=genomic_max,
)
gp.translate(0, y)
if i < len(pre_transcript.translations) - 1:
y += config.inner_margin
y += gp.height
main_group.add(gp)
y += config.breakpoint_bottom_margin if breakpoints else 0
# add masks
for mask in masks:
pixel = mapping.convert_ratioed_pos(
mask.start) | mapping.convert_ratioed_pos(mask.end)
m = canvas.rect(
(pixel.start, 0),
(pixel.length(), y),
class_='mask',
fill=config.mask_fill,
opacity=config.mask_opacity,
pointer_events='none',
)
main_group.add(m)
# now overlay the breakpoints on top of everything
for i, b in enumerate(breakpoints):
pixel = mapping.convert_ratioed_pos(
b.start) | mapping.convert_ratioed_pos(b.end)
bg = draw_breakpoint(
config,
canvas,
b,
pixel.length(),
y,
label=labels.add(b, config.breakpoint_label_prefix),
)
bg.translate(pixel.start, 0)
main_group.add(bg)
setattr(main_group, 'height', y)
setattr(
main_group,
'width',
mapping.convert_ratioed_pos(genomic_min).start -
mapping.convert_ratioed_pos(genomic_max).end,
)
setattr(main_group, 'mapping', mapping)
setattr(main_group, 'labels', labels)
return main_group
def draw_transcript_with_translation(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
translation,
labels,
colors,
mapping: IntervalMapping,
reference_genome=None,
genomic_min=None,
genomic_max=None,
) -> svgwrite.container.Group:
main_group = canvas.g()
pre_transcript = translation.transcript.reference_object
spl_tx = translation.transcript
genomic_min = (pre_transcript.start if genomic_min is None else min(
pre_transcript.start, genomic_min))
genomic_max = (pre_transcript.end if genomic_max is None else max(
pre_transcript.end, genomic_max))
label_prefix = config.transcript_label_prefix
if isinstance(pre_transcript, FusionTranscript):
label_prefix = config.fusion_label_prefix
# if the splicing takes up more room than the track we need to adjust for it
y = config.splice_height
exon_track_group = draw_exon_track(
config,
canvas,
pre_transcript,
mapping,
colors,
translation=translation,
genomic_min=genomic_min,
genomic_max=genomic_max,
)
# calculate the outer pixel boundaries for the exon track
leftmost_ex_px = mapping.convert_ratioed_pos(pre_transcript.start)
leftmost_ex_px = (leftmost_ex_px.start if pre_transcript.start
== genomic_min else leftmost_ex_px.end)
rightmost_ex_px = mapping.convert_ratioed_pos(pre_transcript.end)
rightmost_ex_px = (rightmost_ex_px.end if pre_transcript.end == genomic_max
else rightmost_ex_px.start)
exon_track_group.translate(0, y)
exon_track_group.add(
canvas.text(
labels.add(spl_tx, label_prefix),
insert=(
0 - config.padding,
config.track_height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=config.label_color,
style=config.font_style.format(font_size=config.label_font_size,
text_anchor='end'),
class_='label',
))
exon_track_group.add(
Tag(
'title', 'Transcript: {}'.format(
pre_transcript.name if pre_transcript.name else '')))
# draw the splicing pattern
splice_group = canvas.g(class_='splicing')
for p1, p2 in zip(spl_tx.splicing_pattern[::2],
spl_tx.splicing_pattern[1::2]):
if abs(p1.pos -
p2.pos) < 2: # do not add splicing marks for consecutive exons
continue
a = mapping.convert_ratioed_pos(p1.pos).start
b = mapping.convert_ratioed_pos(p2.pos).end
polyline = [(a, y), (a + (b - a) / 2, y - config.splice_height),
(b, y)]
p = canvas.polyline(polyline, fill='none')
p.dasharray(config.splice_stroke_dasharray)
p.stroke(config.splice_color, width=config.splice_stroke_width)
splice_group.add(p)
y += config.track_height / 2
main_group.add(splice_group)
main_group.add(exon_track_group)
y += config.track_height / 2
protein_group = canvas.g(class_='protein')
y += config.padding
protein_group.translate(0, y)
# translation track
# convert the AA position to cdna position, then convert the cdna to genomic, etc
# ==================== adding the translation track ============
translated_genomic_regions = [
spl_tx.convert_cdna_to_genomic(translation.start),
spl_tx.convert_cdna_to_genomic(translation.end),
]
translated_genomic_regions = [
Interval(*sorted(translated_genomic_regions))
]
for p1, p2 in zip(spl_tx.splicing_pattern[::2],
spl_tx.splicing_pattern[1::2]):
try:
spliced_out_interval = Interval(p1.pos + 1, p2.pos - 1)
temp = []
for region in translated_genomic_regions:
temp.extend(region - spliced_out_interval)
translated_genomic_regions = temp
except AttributeError:
pass
gt = canvas.g(class_='translation')
protein_group.add(gt)
h = config.translation_track_height
leftmost_tx_px = None
rightmost_tx_px = None
for sec in translated_genomic_regions:
start = mapping.convert_ratioed_pos(sec.start)
start = start.start if sec.start == pre_transcript.start else start.end
end = mapping.convert_ratioed_pos(sec.end)
end = end.end if sec.end == pre_transcript.end else end.start
gt.add(
canvas.rect(
(start, h / 2 - config.translation_track_height / 2),
(end - start + 1, config.translation_track_height),
fill=config.translation_scaffold_color,
class_='scaffold',
))
leftmost_tx_px = (min(start, end) if leftmost_tx_px is None else min(
start, end, leftmost_tx_px))
rightmost_tx_px = (max(start, end) if rightmost_tx_px is None else max(
start, end, rightmost_tx_px))
gt.add(
canvas.text(
config.translation_end_marker if spl_tx.get_strand() == STRAND.NEG
else config.translation_start_marker,
insert=(
leftmost_tx_px - config.translation_marker_padding,
h / 2 +
config.font_central_shift_ratio * config.translation_font_size,
),
fill=config.label_color,
style=config.font_style.format(
font_size=config.translation_font_size, text_anchor='end'),
class_='label',
))
gt.add(
canvas.text(
config.translation_start_marker if spl_tx.get_strand()
== STRAND.NEG else config.translation_end_marker,
insert=(
rightmost_tx_px + config.translation_marker_padding,
h / 2 +
config.font_central_shift_ratio * config.translation_font_size,
),
fill=config.label_color,
style=config.font_style.format(
font_size=config.translation_font_size, text_anchor='start'),
class_='label',
))
gt.add(
Tag(
'title',
'translation cdna({}_{}) c.{}_{} p.{}_{}'.format(
translation.start,
translation.end,
1,
len(translation),
1,
len(translation) // CODON_SIZE,
),
))
py = h
# now draw the domain tracks
# need to convert the domain AA positions to cds positions to genomic
for i, d in enumerate(sorted(translation.domains, key=lambda x: x.name)):
if not re.match(config.domain_name_regex_filter, str(d.name)):
continue
py += config.padding
domain_group = canvas.g(class_='domain')
domain_group.add(
canvas.rect(
(leftmost_ex_px, config.domain_track_height / 2),
(rightmost_ex_px - leftmost_ex_px,
config.domain_scaffold_height),
fill=config.domain_scaffold_color,
class_='scaffold',
))
fill = config.domain_color
percent_match = None
try:
match, total = d.score_region_mapping(reference_genome)
percent_match = int(round(match * 100 / total, 0))
fill = config.domain_fill_gradient[
percent_match % len(config.domain_fill_gradient) - 1]
except (NotSpecifiedError, AttributeError):
pass
for region in d.regions:
# convert the AA position to cdna position, then convert the cdna to genomic, etc
s = translation.convert_aa_to_cdna(region.start)
t = translation.convert_aa_to_cdna(region.end)
s = mapping.convert_pos(spl_tx.convert_cdna_to_genomic(s.start))
t = mapping.convert_pos(spl_tx.convert_cdna_to_genomic(t.end))
if s > t:
t, s = (s, t)
domain_region_group = canvas.g(class_='domain_region')
domain_region_group.add(
canvas.rect((s, 0), (t - s + 1, config.domain_track_height),
fill=fill,
class_='region'))
domain_region_group.add(
Tag(
'title',
'domain {} region p.{}_{}{}'.format(
d.name if d.name else '',
region.start,
region.end,
' matched({}%)'.format(percent_match)
if percent_match is not None else '',
),
))
domain_group.add(domain_region_group)
domain_group.translate(0, py)
f = (config.label_color if not config.dynamic_labels else
dynamic_label_color(config.domain_color))
label_group = None
for patt, link in config.domain_links.items():
if re.match(patt, d.name):
label_group = canvas.a(link.format(d), target='_blank')
break
if label_group is None:
label_group = canvas.g()
domain_group.add(label_group)
label_group.add(
canvas.text(
labels.add(d.name, config.domain_label_prefix),
insert=(
0 - config.padding,
config.domain_track_height / 2 +
config.font_central_shift_ratio *
config.domain_label_font_size,
),
fill=f,
class_='label',
style=config.font_style.format(
font_size=config.domain_label_font_size,
text_anchor='end'),
))
protein_group.add(domain_group)
py += config.domain_track_height
y += py
main_group.add(protein_group)
setattr(main_group, 'height', y)
return main_group
def draw_gene(
config: DiagramSettings,
canvas: svgwrite.drawing.Drawing,
gene: 'Gene',
width: int,
height: int,
fill: str,
label: str = '',
) -> svgwrite.container.Group:
"""
generates the svg object representing a gene
Args:
canvas: the main svgwrite object used to create new svg elements
gene: the gene to draw
width: the pixel width
height: the pixel height
fill: the fill color to use for the gene
Return:
the group element for the diagram
"""
group = canvas.g(class_='gene')
if width < config.gene_min_width:
raise DrawingFitError(
'width of {} is not sufficient to draw a gene of minimum width {}'.
format(width, config.gene_min_width),
gene,
)
wrect = width - config.gene_arrow_width
if wrect < 1:
raise DrawingFitError('width is not sufficient to draw gene')
label_color = config.label_color if not config.dynamic_labels else dynamic_label_color(
fill)
if gene.get_strand() == STRAND.POS:
group.add(canvas.rect((0, 0), (wrect, height), fill=fill))
group.add(
canvas.polyline(
[(wrect, 0), (wrect + config.gene_arrow_width, height / 2),
(wrect, height)],
fill=fill,
))
group.add(
canvas.text(
label,
insert=(
wrect / 2,
height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=label_color,
style=config.font_style.format(
font_size=config.label_font_size, text_anchor='middle'),
class_='label',
))
elif gene.get_strand() == STRAND.NEG:
group.add(
canvas.rect((config.gene_arrow_width, 0), (wrect, height),
fill=fill))
group.add(
canvas.polyline(
[(config.gene_arrow_width, 0), (0, height / 2),
(config.gene_arrow_width, height)],
fill=fill,
))
group.add(
canvas.text(
label,
insert=(
wrect / 2 + config.gene_arrow_width,
height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=label_color,
style=config.font_style.format(
font_size=config.label_font_size, text_anchor='middle'),
class_='label',
))
else:
group.add(canvas.rect((0, 0), (width, height), fill=fill))
group.add(
canvas.text(
label,
insert=(
width / 2,
height / 2 +
config.font_central_shift_ratio * config.label_font_size,
),
fill=label_color,
style=config.font_style.format(
font_size=config.label_font_size, text_anchor='middle'),
class_='label',
))
aliases = ''
try:
if gene.aliases:
aliases = ' aka {}'.format(';'.join(sorted(gene.aliases)))
except AttributeError:
pass
group.add(
Tag(
'title',
'Gene {} {}:g.{}_{}{}{}'.format(
gene.name if gene.name else '',
gene.chr,
gene.start,
gene.end,
gene.get_strand(),
aliases,
),
))
return group