def report(args):
"""
%prog report [--options] ace_file > report
Prepare a report of read location, consensus location or quality segment per contig
"""
from jcvi.utils.table import tabulate
p = OptionParser(report.__doc__)
types = {"read": ["padded_start", "padded_end", "orient"],
"consensus": ["padded_consensus_start", "padded_consensus_end"],
"quality" : ["qual_clipping_start", "qual_clipping_end", "align_clipping_start", "align_clipping_end"]
}
valid_types = tuple(types.keys())
p.add_option("--type", default="read", choices=valid_types,
help="choose report type [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(not p.print_help())
acefile, = args
ace = Ace.read(must_open(acefile))
logging.debug('Loaded ace file {0}'.format(acefile))
for c in ace.contigs:
print c.name
table = dict()
if opts.type == "read":
ps, pe = [], []
ps = [read.padded_start for read in c.af]
for i in xrange(1, len(ps)):
pe.append(ps[i] - ps[i-1])
pe.append(c.nbases)
map = dict(zip(ps, pe))
for i, read in enumerate(c.af):
values = [str(x) for x in (read.padded_start, map[read.padded_start], read.coru)]
for i, label in enumerate(types[opts.type]):
table[(str(read.name), label)] = values[i]
elif opts.type == "consensus":
for read in c.bs:
values = [str(x) for x in (read.padded_start, read.padded_end)]
for i, label in enumerate(types[opts.type]):
table[(str(read.name), label)] = values[i]
elif opts.type == "quality":
for read in c.reads:
(r1, r2) = (read.rd, read.qa)
values = [str(x) for x in (r2.qual_clipping_start, r2.qual_clipping_end, r2.align_clipping_start, r2.align_clipping_end)]
for i, label in enumerate(types[opts.type]):
table[(str(r1.name), label)] = values[i]
print tabulate(table), "\n"
def report(args):
"""
%prog report [--options] ace_file > report
Prepare a report of read location, consensus location or quality segment per contig
"""
from jcvi.utils.table import tabulate
p = OptionParser(report.__doc__)
types = {"read": ["padded_start", "padded_end", "orient"],
"consensus": ["padded_consensus_start", "padded_consensus_end"],
"quality" : ["qual_clipping_start", "qual_clipping_end", "align_clipping_start", "align_clipping_end"]
}
valid_types = tuple(types.keys())
p.add_option("--type", default="read", choices=valid_types,
help="choose report type [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(not p.print_help())
acefile, = args
ace = Ace.read(must_open(acefile))
logging.debug('Loaded ace file {0}'.format(acefile))
for c in ace.contigs:
print c.name
table = dict()
if opts.type == "read":
ps, pe = [], []
ps = [read.padded_start for read in c.af]
for i in xrange(1, len(ps)):
pe.append(ps[i] - ps[i-1])
pe.append(c.nbases)
map = dict(zip(ps, pe))
for i, read in enumerate(c.af):
values = [str(x) for x in (read.padded_start, map[read.padded_start], read.coru)]
for i, label in enumerate(types[opts.type]):
table[(str(read.name), label)] = values[i]
elif opts.type == "consensus":
for read in c.bs:
values = [str(x) for x in (read.padded_start, read.padded_end)]
for i, label in enumerate(types[opts.type]):
table[(str(read.name), label)] = values[i]
elif opts.type == "quality":
for read in c.reads:
(r1, r2) = (read.rd, read.qa)
values = [str(x) for x in (r2.qual_clipping_start, r2.qual_clipping_end, r2.align_clipping_start, r2.align_clipping_end)]
for i, label in enumerate(types[opts.type]):
table[(str(r1.name), label)] = values[i]
print tabulate(table), "\n"
def summary(args):
"""
%prog summary input.bed scaffolds.fasta
Print out summary statistics per map, followed by consensus summary of
scaffold anchoring based on multiple maps.
"""
p = OptionParser(summary.__doc__)
p.set_table(sep="|", align=True)
p.set_outfile()
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
inputbed, scaffolds = args
pf = inputbed.rsplit(".", 1)[0]
mapbed = pf + ".bed"
chr_agp = pf + ".chr.agp"
sep = opts.sep
align = opts.align
cc = Map(mapbed)
mapnames = cc.mapnames
s = Sizes(scaffolds)
total, l50, n50 = s.summary
r = {}
maps = []
fw = must_open(opts.outfile, "w")
print >> fw, "*** Summary for each individual map ***"
for mapname in mapnames:
markers = [x for x in cc if x.mapname == mapname]
ms = MapSummary(markers, l50, s)
r["Linkage Groups", mapname] = ms.num_lgs
ms.export_table(r, mapname, total)
maps.append(ms)
print >> fw, tabulate(r, sep=sep, align=align)
r = {}
agp = AGP(chr_agp)
print >> fw, "*** Summary for consensus map ***"
consensus_scaffolds = set(x.component_id for x in agp if not x.is_gap)
oriented_scaffolds = set(x.component_id for x in agp \
if (not x.is_gap) and x.orientation != '?')
unplaced_scaffolds = set(s.mapping.keys()) - consensus_scaffolds
for mapname, sc in (("Anchored", consensus_scaffolds),
("Oriented", oriented_scaffolds),
("Unplaced", unplaced_scaffolds)):
markers = [x for x in cc if x.seqid in sc]
ms = MapSummary(markers, l50, s, scaffolds=sc)
ms.export_table(r, mapname, total)
print >> fw, tabulate(r, sep=sep, align=align)
def summary(args):
"""
%prog summary input.bed scaffolds.fasta
Print out summary statistics per map, followed by consensus summary of
scaffold anchoring based on multiple maps.
"""
p = OptionParser(summary.__doc__)
p.set_table(sep="|", align=True)
p.set_outfile()
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
inputbed, scaffolds = args
pf = inputbed.rsplit(".", 1)[0]
mapbed = pf + ".bed"
chr_agp = pf + ".chr.agp"
sep = opts.sep
align = opts.align
cc = Map(mapbed)
mapnames = cc.mapnames
s = Sizes(scaffolds)
total, l50, n50 = s.summary
r = {}
maps = []
fw = must_open(opts.outfile, "w")
print >> fw, "*** Summary for each individual map ***"
for mapname in mapnames:
markers = [x for x in cc if x.mapname == mapname]
ms = MapSummary(markers, l50, s)
r["Linkage Groups", mapname] = ms.num_lgs
ms.export_table(r, mapname, total)
maps.append(ms)
print >> fw, tabulate(r, sep=sep, align=align)
r = {}
agp = AGP(chr_agp)
print >> fw, "*** Summary for consensus map ***"
consensus_scaffolds = set(x.component_id for x in agp if not x.is_gap)
unplaced_scaffolds = set(s.mapping.keys()) - consensus_scaffolds
for mapname, sc in (("Anchored", consensus_scaffolds),
("Unplaced", unplaced_scaffolds)):
markers = [x for x in cc if x.seqid in sc]
ms = MapSummary(markers, l50, s, scaffolds=sc)
ms.export_table(r, mapname, total)
print >> fw, tabulate(r, sep=sep, align=align)
def allstats(args):
"""
%prog allstats fastafiles
Summarize multiple FASTA in a table.
"""
from jcvi.utils.table import tabulate
p = OptionParser(allstats.__doc__)
p.add_option("--exclude", help="Exclude statistics, must be {0}, "
"multiple separated by comma [default: %default]".\
format("|".join(header))
)
opts, args = p.parse_args(args)
if len(args) < 1:
sys.exit(not p.print_help())
fastafiles = args
exclude = opts.exclude.split(",")
assert all(x in header for x in exclude)
tabledict = {}
for fastafile in fastafiles:
pf = fastafile.rsplit(".", 1)[0]
for key, val in n50([fastafile]):
if key in exclude:
continue
tabledict[(pf, key)] = val
table = tabulate(tabledict)
print >> sys.stderr, table
def test_tabulate():
from jcvi.utils.table import tabulate
data = {(1, "a"): 3, (1, "b"): 4, (2, "a"): 5, (2, "b"): 0}
assert (tabulate(data) == """===========
o a b
-----------
1 3 4
2 5 0
-----------""")
assert (tabulate(data, transpose=True) == """===========
o 1 2
-----------
a 3 5
b 4 0
-----------""")
def summary(args):
"""
%prog summary *.gff
Print gene statistics table.
"""
p = OptionParser(summary.__doc__)
opts, args = p.parse_args(args)
if len(args) < 1:
sys.exit(not p.print_help())
gff_files = args
for metric in metrics:
logging.debug("Parsing files in `{0}`..".format(metric))
table = {}
for x in gff_files:
pf = op.basename(x).split(".")[0]
numberfile = op.join(metric, pf + ".txt")
ar = [int(x.strip()) for x in open(numberfile)]
sum = SummaryStats(ar).todict().items()
keys, vals = zip(*sum)
keys = [(pf, x) for x in keys]
table.update(dict(zip(keys, vals)))
print >> sys.stderr, tabulate(table)
def summary(args):
"""
%prog summary *.gff
Print gene statistics table.
"""
from jcvi.utils.table import tabulate
p = OptionParser(summary.__doc__)
opts, args = p.parse_args(args)
if len(args) < 1:
sys.exit(not p.print_help())
gff_files = args
for metric in metrics:
logging.debug("Parsing files in `{0}`..".format(metric))
table = {}
for x in gff_files:
pf = op.basename(x).split(".")[0]
numberfile = op.join(metric, pf + ".txt")
ar = [int(x.strip()) for x in open(numberfile)]
sum = SummaryStats(ar).todict().items()
keys, vals = zip(*sum)
keys = [(pf, x) for x in keys]
table.update(dict(zip(keys, vals)))
print >> sys.stderr, tabulate(table)
def summary(args):
"""
%prog summary gffile fastafile
Print summary stats, including:
- Gene/Exon/Intron
- Number
- Average size (bp)
- Median size (bp)
- Total length (Mb)
- % of genome
- % GC
"""
p = OptionParser(summary.__doc__)
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
gff_file, ref = args
s = Fasta(ref)
g = make_index(gff_file)
geneseqs, exonseqs, intronseqs = [], [], [] # Calc % GC
for f in g.features_of_type("gene"):
fid = f.id
fseq = s.sequence({'chr': f.chrom, 'start': f.start, 'stop': f.stop})
geneseqs.append(fseq)
exons = set((c.chrom, c.start, c.stop) for c in g.children(fid, 2) \
if c.featuretype == "exon")
exons = list(exons)
for chrom, start, stop in exons:
fseq = s.sequence({'chr': chrom, 'start': start, 'stop': stop})
exonseqs.append(fseq)
introns = range_interleave(exons)
for chrom, start, stop in introns:
fseq = s.sequence({'chr': chrom, 'start': start, 'stop': stop})
intronseqs.append(fseq)
r = {} # Report
for t, tseqs in zip(("Gene", "Exon", "Intron"),
(geneseqs, exonseqs, intronseqs)):
tsizes = [len(x) for x in tseqs]
tsummary = SummaryStats(tsizes, dtype="int")
r[t, "Number"] = tsummary.size
r[t, "Average size (bp)"] = tsummary.mean
r[t, "Median size (bp)"] = tsummary.median
r[t, "Total length (Mb)"] = human_size(tsummary.sum,
precision=0,
target="Mb")
r[t, "% of genome"] = percentage(tsummary.sum,
s.totalsize,
precision=0,
mode=-1)
r[t, "% GC"] = gc(tseqs)
print >> sys.stderr, tabulate(r)
def script(args):
"""
%prog script bfs_rfs libs
`bfs_rfs` contains the joined results from Brian's `classifyMates`. We want
to keep the RFS result (but not in the BFS result) to retain actual MP. Libs
contain a list of lib iids, use comma to separate, e.g. "9,10,11".
"""
p = OptionParser(script.__doc__)
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(p.print_help())
fsfile, libs = args
libs = [int(x) for x in libs.split(",")]
fp = open(fsfile)
not_found = ("limited", "exhausted")
counts = defaultdict(int)
pe, mp = 0, 0
both, noidea = 0, 0
total = 0
for i in libs:
print "lib iid {0} allfragsunmated 1".format(i)
for row in fp:
frgiid, bfs, rfs = row.split()
bfs = (bfs not in not_found)
rfs = (rfs not in not_found)
if bfs and (not rfs):
pe += 1
if rfs and (not bfs):
mp += 1
frgiid = int(frgiid)
mateiid = frgiid + 1
print "frg iid {0} mateiid {1}".format(frgiid, mateiid)
print "frg iid {0} mateiid {1}".format(mateiid, frgiid)
if bfs and rfs:
both += 1
if (not bfs) and (not rfs):
noidea += 1
total += 1
assert pe + mp + both + noidea == total
counts[("PE", "N")] = pe
counts[("MP", "N")] = mp
counts[("Both", "N")] = both
counts[("No Idea", "N")] = noidea
table = tabulate(counts)
func = lambda a: a * 100. / total
table = table.withNewColumn("Percentage", callback=func,
columns=("N",), digits=2)
print >> sys.stderr, table
def script(args):
"""
%prog script bfs_rfs libs
`bfs_rfs` contains the joined results from Brian's `classifyMates`. We want
to keep the RFS result (but not in the BFS result) to retain actual MP. Libs
contain a list of lib iids, use comma to separate, e.g. "9,10,11".
"""
p = OptionParser(script.__doc__)
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(p.print_help())
fsfile, libs = args
libs = [int(x) for x in libs.split(",")]
fp = open(fsfile)
not_found = ("limited", "exhausted")
counts = defaultdict(int)
pe, mp = 0, 0
both, noidea = 0, 0
total = 0
for i in libs:
print "lib iid {0} allfragsunmated 1".format(i)
for row in fp:
frgiid, bfs, rfs = row.split()
bfs = (bfs not in not_found)
rfs = (rfs not in not_found)
if bfs and (not rfs):
pe += 1
if rfs and (not bfs):
mp += 1
frgiid = int(frgiid)
mateiid = frgiid + 1
print "frg iid {0} mateiid {1}".format(frgiid, mateiid)
print "frg iid {0} mateiid {1}".format(mateiid, frgiid)
if bfs and rfs:
both += 1
if (not bfs) and (not rfs):
noidea += 1
total += 1
assert pe + mp + both + noidea == total
counts[("PE", "N")] = pe
counts[("MP", "N")] = mp
counts[("Both", "N")] = both
counts[("No Idea", "N")] = noidea
table = tabulate(counts)
func = lambda a: a * 100. / total
table = table.withNewColumn("Percentage", callback=func,
columns=("N",), digits=2)
print >> sys.stderr, table
def stats(args):
"""
%prog stats agpfile
Print out a report for length of gaps and components.
"""
p = OptionParser(stats.__doc__)
p.add_option("--warn",
default=False,
action="store_true",
help="Warnings on small component spans [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(p.print_help())
agpfile, = args
agp = AGP(agpfile)
gap_lengths = []
component_lengths = []
for a in agp:
span = a.object_span
if a.is_gap:
label = a.gap_type
gap_lengths.append((span, label))
else:
label = "{0}:{1}-{2}".format(a.component_id, a.component_beg, \
a.component_end)
component_lengths.append((span, label))
if opts.warn and span < 50:
logging.error("component span too small ({0}):\n{1}".\
format(span, a))
table = dict()
for label, lengths in zip(("Gaps", "Components"),
(gap_lengths, component_lengths)):
if not lengths:
table[(label, "Min")] = table[(label, "Max")] \
= table[(label, "Sum")] = "n.a."
continue
table[(label, "Min")] = "{0} ({1})".format(*min(lengths))
table[(label, "Max")] = "{0} ({1})".format(*max(lengths))
table[(label, "Sum")] = sum(x[0] for x in lengths)
from jcvi.utils.table import tabulate
table = tabulate(table)
print >> sys.stderr, table
def summary(args):
"""
%prog summary gffile fastafile
Print summary stats, including:
- Gene/Exon/Intron
- Number
- Average size (bp)
- Median size (bp)
- Total length (Mb)
- % of genome
- % GC
"""
p = OptionParser(summary.__doc__)
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
gff_file, ref = args
s = Fasta(ref)
g = make_index(gff_file)
geneseqs, exonseqs, intronseqs = [], [], [] # Calc % GC
for f in g.features_of_type("gene"):
fid = f.id
fseq = s.sequence({'chr': f.chrom, 'start': f.start, 'stop': f.stop})
geneseqs.append(fseq)
exons = set((c.chrom, c.start, c.stop) for c in g.children(fid, 2) \
if c.featuretype == "exon")
exons = list(exons)
for chrom, start, stop in exons:
fseq = s.sequence({'chr': chrom, 'start': start, 'stop': stop})
exonseqs.append(fseq)
introns = range_interleave(exons)
for chrom, start, stop in introns:
fseq = s.sequence({'chr': chrom, 'start': start, 'stop': stop})
intronseqs.append(fseq)
r = {} # Report
for t, tseqs in zip(("Gene", "Exon", "Intron"), (geneseqs, exonseqs, intronseqs)):
tsizes = [len(x) for x in tseqs]
tsummary = SummaryStats(tsizes, dtype="int")
r[t, "Number"] = tsummary.size
r[t, "Average size (bp)"] = tsummary.mean
r[t, "Median size (bp)"] = tsummary.median
r[t, "Total length (Mb)"] = human_size(tsummary.sum, precision=0, target="Mb")
r[t, "% of genome"] = percentage(tsummary.sum, s.totalsize, precision=0, mode=-1)
r[t, "% GC"] = gc(tseqs)
print(tabulate(r), file=sys.stderr)
def __str__(self):
from jcvi.utils.table import tabulate
table = {}
table[("Prediction-True", "Reality-True")] = self.TP
table[("Prediction-True", "Reality-False")] = self.FP
table[("Prediction-False", "Reality-True")] = self.FN
table[("Prediction-False", "Reality-False")] = self.TN
msg = str(tabulate(table))
msg += "\nSensitivity [TP / (TP + FN)]: {0:.1f} %\n".format(self.sensitivity * 100)
msg += "Specificity [TP / (TP + FP)]: {0:.1f} %\n".format(self.specificity * 100)
msg += "Accuracy [(TP + TN) / (TP + FP + FN + TN)]: {0:.1f} %".format(self.accuracy * 100)
return msg
def stats(args):
"""
%prog stats agpfile
Print out a report for length of gaps and components.
"""
p = OptionParser(stats.__doc__)
p.add_option("--warn", default=False, action="store_true",
help="Warnings on small component spans [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(p.print_help())
agpfile, = args
agp = AGP(agpfile)
gap_lengths = []
component_lengths = []
for a in agp:
span = a.object_span
if a.is_gap:
label = a.gap_type
gap_lengths.append((span, label))
else:
label = "{0}:{1}-{2}".format(a.component_id, a.component_beg, \
a.component_end)
component_lengths.append((span, label))
if opts.warn and span < 50:
logging.error("component span too small ({0}):\n{1}".\
format(span, a))
table = dict()
for label, lengths in zip(("Gaps", "Components"),
(gap_lengths, component_lengths)):
if not lengths:
table[(label, "Min")] = table[(label, "Max")] \
= table[(label, "Sum")] = "n.a."
continue
table[(label, "Min")] = "{0} ({1})".format(*min(lengths))
table[(label, "Max")] = "{0} ({1})".format(*max(lengths))
table[(label, "Sum")] = sum(x[0] for x in lengths)
from jcvi.utils.table import tabulate
table = tabulate(table)
print >> sys.stderr, table
def __str__(self):
from jcvi.utils.table import tabulate
table = {}
table[("Prediction-True", "Reality-True")] = self.TP
table[("Prediction-True", "Reality-False")] = self.FP
table[("Prediction-False", "Reality-True")] = self.FN
table[("Prediction-False", "Reality-False")] = self.TN
msg = str(tabulate(table))
msg += "\nSensitivity [TP / (TP + FN)]: {0:.1f} %\n".\
format(self.sensitivity * 100)
msg += "Specificity [TP / (TP + FP)]: {0:.1f} %\n".\
format(self.specificity * 100)
msg += "Accuracy [(TP + TN) / (TP + FP + FN + TN)]: {0:.1f} %".\
format(self.accuracy * 100)
return msg
def genestats(args):
"""
%prog genestats gffile
Print summary stats, including:
- Number of genes
- Number of single-exon genes
- Number of multi-exon genes
- Number of distinct exons
- Number of genes with alternative transcript variants
- Number of predicted transcripts
- Mean number of distinct exons per gene
- Mean number of transcripts per gene
- Mean gene locus size (first to last exon)
- Mean transcript size (UTR, CDS)
- Mean exon size
Stats modeled after barley genome paper Table 1.
A physical, genetic and functional sequence assembly of the barley genome
"""
p = OptionParser(genestats.__doc__)
p.add_option("--groupby", default="conf_class",
help="Print separate stats groupby")
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(not p.print_help())
gff_file, = args
gb = opts.groupby
g = make_index(gff_file)
tf = "transcript.sizes"
if need_update(gff_file, tf):
fw = open(tf, "w")
for feat in g.features_of_type("mRNA"):
fid = feat.id
conf_class = feat.attributes.get(gb, "all")
tsize = sum((c.stop - c.start + 1) for c in g.children(fid, 1) \
if c.featuretype == "exon")
print >> fw, "\t".join((fid, str(tsize), conf_class))
fw.close()
tsizes = DictFile(tf, cast=int)
conf_classes = DictFile(tf, valuepos=2)
logging.debug("A total of {0} transcripts populated.".format(len(tsizes)))
genes = []
for feat in g.features_of_type("gene"):
fid = feat.id
transcripts = [c.id for c in g.children(fid, 1) \
if c.featuretype == "mRNA"]
transcript_sizes = [tsizes[x] for x in transcripts]
exons = set((c.chrom, c.start, c.stop) for c in g.children(fid, 2) \
if c.featuretype == "exon")
conf_class = conf_classes[transcripts[0]]
gs = GeneStats(feat, conf_class, transcript_sizes, exons)
genes.append(gs)
r = {} # Report
distinct_groups = set(conf_classes.values())
for g in distinct_groups:
num_genes = num_single_exon_genes = num_multi_exon_genes = 0
num_genes_with_alts = num_transcripts = num_exons = 0
cum_locus_size = cum_transcript_size = cum_exon_size = 0
for gs in genes:
if gs.conf_class != g:
continue
num_genes += 1
if gs.num_exons == 1:
num_single_exon_genes += 1
else:
num_multi_exon_genes += 1
num_exons += gs.num_exons
if gs.num_transcripts > 1:
num_genes_with_alts += 1
num_transcripts += gs.num_transcripts
cum_locus_size += gs.locus_size
cum_transcript_size += gs.cum_transcript_size
cum_exon_size += gs.cum_exon_size
mean_num_exons = num_exons * 1. / num_genes
mean_num_transcripts = num_transcripts * 1. / num_genes
mean_locus_size = cum_locus_size * 1. / num_genes
mean_transcript_size = cum_transcript_size * 1. / num_transcripts
mean_exon_size = cum_exon_size * 1. / num_exons
r[("Number of genes", g)] = num_genes
r[("Number of single-exon genes", g)] = \
percentage(num_single_exon_genes, num_genes, mode=1)
r[("Number of multi-exon genes", g)] = \
percentage(num_multi_exon_genes, num_genes, mode=1)
r[("Number of distinct exons", g)] = num_exons
r[("Number of genes with alternative transcript variants", g)] = \
percentage(num_genes_with_alts, num_genes, mode=1)
r[("Number of predicted transcripts", g)] = num_transcripts
r[("Mean number of distinct exons per gene", g)] = mean_num_exons
r[("Mean number of transcripts per gene", g)] = mean_num_transcripts
r[("Mean gene locus size (first to last exon)", g)] = mean_locus_size
r[("Mean transcript size (UTR, CDS)", g)] = mean_transcript_size
r[("Mean exon size", g)] = mean_exon_size
print >> sys.stderr, tabulate(r)
def summary(args):
"""
%prog summary txtfile fastafile
The txtfile can be generated by: %prog mstmap --noheader --freq=0
Tabulate on all possible combinations of genotypes and provide results
in a nicely-formatted table. Give a fastafile for SNP rate (average
# of SNPs per Kb).
Only three-column file is supported:
locus_id intra- genotype inter- genotype
"""
from jcvi.utils.cbook import thousands
from jcvi.utils.table import tabulate
p = OptionParser(summary.__doc__)
p.add_option("--counts",
help="Print SNP counts in a txt file [default: %default]")
p.add_option("--bed",
help="Print SNPs locations in a bed file [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
txtfile, fastafile = args
bedfw = open(opts.bed, "w") if opts.bed else None
fp = open(txtfile)
header = fp.next().split() # Header
snps = defaultdict(list) # contig => list of loci
combinations = defaultdict(int)
intraSNPs = interSNPs = 0
distinctSet = set() # set of genes that show A-B pattern
ref, alt = header[1:3]
snpcounts, goodsnpcounts = defaultdict(int), defaultdict(int)
for row in fp:
atoms = row.split()
assert len(atoms) == 3, \
"Only three-column file is supported"
locus, intra, inter = atoms
ctg, pos = locus.rsplit(".", 1)
pos = int(pos)
snps[ctg].append(pos)
snpcounts[ctg] += 1
if intra == 'X':
intraSNPs += 1
if inter in ('B', 'X'):
interSNPs += 1
if intra == 'A' and inter == 'B':
distinctSet.add(ctg)
goodsnpcounts[ctg] += 1
# Tabulate all possible combinations
intra = ref + "-" + intra
inter = alt + "-" + inter
combinations[(intra, inter)] += 1
if bedfw:
print >> bedfw, "\t".join(str(x) for x in \
(ctg, pos - 1, pos, locus))
if bedfw:
logging.debug("SNP locations written to `{0}`.".format(opts.bed))
bedfw.close()
nsites = sum(len(x) for x in snps.values())
sizes = Sizes(fastafile)
bpsize = sizes.totalsize
snprate = lambda a: a * 1000. / bpsize
m = "Dataset `{0}` contains {1} contigs ({2} bp).\n".\
format(fastafile, len(sizes), thousands(bpsize))
m += "A total of {0} SNPs within {1} contigs ({2} bp).\n".\
format(nsites, len(snps),
thousands(sum(sizes.mapping[x] for x in snps.keys())))
m += "SNP rate: {0:.1f}/Kb, ".format(snprate(nsites))
m += "IntraSNPs: {0} ({1:.1f}/Kb), InterSNPs: {2} ({3:.1f}/Kb)".\
format(intraSNPs, snprate(intraSNPs), interSNPs, snprate(interSNPs))
print >> sys.stderr, m
print >> sys.stderr, tabulate(combinations)
leg = "Legend: A - homozygous same, B - homozygous different, X - heterozygous"
print >> sys.stderr, leg
tag = (ref + "-A", alt + "-B")
distinctSNPs = combinations[tag]
tag = str(tag).replace("'", "")
print >> sys.stderr, "A total of {0} disparate {1} SNPs in {2} contigs.".\
format(distinctSNPs, tag, len(distinctSet))
if not opts.counts:
return
snpcountsfile = opts.counts
fw = open(snpcountsfile, "w")
header = "\t".join(("Contig", "#_SNPs", "#_AB_SNP"))
print >> fw, header
assert sum(snpcounts.values()) == nsites
assert sum(goodsnpcounts.values()) == distinctSNPs
for ctg in sorted(snps.keys()):
snpcount = snpcounts[ctg]
goodsnpcount = goodsnpcounts[ctg]
print >> fw, "\t".join(str(x) for x in (ctg, snpcount, goodsnpcount))
fw.close()
logging.debug("SNP counts per contig is written to `{0}`.".\
format(snpcountsfile))
def summary(args):
"""
%prog summary txtfile fastafile
The txtfile can be generated by: %prog mstmap --noheader --freq=0
Tabulate on all possible combinations of genotypes and provide results
in a nicely-formatted table. Give a fastafile for SNP rate (average
# of SNPs per Kb).
Only three-column file is supported:
locus_id intra- genotype inter- genotype
"""
from jcvi.utils.cbook import thousands
from jcvi.utils.table import tabulate
p = OptionParser(summary.__doc__)
p.add_option("--counts",
help="Print SNP counts in a txt file [default: %default]")
p.add_option("--bed",
help="Print SNPs locations in a bed file [default: %default]")
opts, args = p.parse_args(args)
if len(args) != 2:
sys.exit(not p.print_help())
txtfile, fastafile = args
bedfw = open(opts.bed, "w") if opts.bed else None
fp = open(txtfile)
header = fp.next().split() # Header
snps = defaultdict(list) # contig => list of loci
combinations = defaultdict(int)
intraSNPs = interSNPs = 0
distinctSet = set() # set of genes that show A-B pattern
ref, alt = header[1:3]
snpcounts, goodsnpcounts = defaultdict(int), defaultdict(int)
for row in fp:
atoms = row.split()
assert len(atoms) == 3, \
"Only three-column file is supported"
locus, intra, inter = atoms
ctg, pos = locus.rsplit(".", 1)
pos = int(pos)
snps[ctg].append(pos)
snpcounts[ctg] += 1
if intra == 'X':
intraSNPs += 1
if inter in ('B', 'X'):
interSNPs += 1
if intra == 'A' and inter == 'B':
distinctSet.add(ctg)
goodsnpcounts[ctg] += 1
# Tabulate all possible combinations
intra = ref + "-" + intra
inter = alt + "-" + inter
combinations[(intra, inter)] += 1
if bedfw:
print >> bedfw, "\t".join(str(x) for x in \
(ctg, pos - 1, pos, locus))
if bedfw:
logging.debug("SNP locations written to `{0}`.".format(opts.bed))
bedfw.close()
nsites = sum(len(x) for x in snps.values())
sizes = Sizes(fastafile)
bpsize = sizes.totalsize
snprate = lambda a: a * 1000. / bpsize
m = "Dataset `{0}` contains {1} contigs ({2} bp).\n".\
format(fastafile, len(sizes), thousands(bpsize))
m += "A total of {0} SNPs within {1} contigs ({2} bp).\n".\
format(nsites, len(snps),
thousands(sum(sizes.mapping[x] for x in snps.keys())))
m += "SNP rate: {0:.1f}/Kb, ".format(snprate(nsites))
m += "IntraSNPs: {0} ({1:.1f}/Kb), InterSNPs: {2} ({3:.1f}/Kb)".\
format(intraSNPs, snprate(intraSNPs), interSNPs, snprate(interSNPs))
print >> sys.stderr, m
print >> sys.stderr, tabulate(combinations)
leg = "Legend: A - homozygous same, B - homozygous different, X - heterozygous"
print >> sys.stderr, leg
tag = (ref + "-A", alt + "-B")
distinctSNPs = combinations[tag]
tag = str(tag).replace("'", "")
print >> sys.stderr, "A total of {0} disparate {1} SNPs in {2} contigs.".\
format(distinctSNPs, tag, len(distinctSet))
if not opts.counts:
return
snpcountsfile = opts.counts
fw = open(snpcountsfile, "w")
header = "\t".join(("Contig", "#_SNPs", "#_AB_SNP"))
print >> fw, header
assert sum(snpcounts.values()) == nsites
assert sum(goodsnpcounts.values()) == distinctSNPs
for ctg in sorted(snps.keys()):
snpcount = snpcounts[ctg]
goodsnpcount = goodsnpcounts[ctg]
print >> fw, "\t".join(str(x) for x in (ctg, snpcount, goodsnpcount))
fw.close()
logging.debug("SNP counts per contig is written to `{0}`.".\
format(snpcountsfile))
def genestats(args):
"""
%prog genestats gffile
Print summary stats, including:
- Number of genes
- Number of single-exon genes
- Number of multi-exon genes
- Number of distinct exons
- Number of genes with alternative transcript variants
- Number of predicted transcripts
- Mean number of distinct exons per gene
- Mean number of transcripts per gene
- Mean gene locus size (first to last exon)
- Mean transcript size (UTR, CDS)
- Mean exon size
Stats modeled after barley genome paper Table 1.
A physical, genetic and functional sequence assembly of the barley genome
"""
p = OptionParser(genestats.__doc__)
p.add_option("--groupby",
default="conf_class",
help="Print separate stats groupby")
p.set_outfile()
opts, args = p.parse_args(args)
if len(args) != 1:
sys.exit(not p.print_help())
gff_file, = args
gb = opts.groupby
g = make_index(gff_file)
tf = "transcript.sizes"
if need_update(gff_file, tf):
fw = open(tf, "w")
for feat in g.features_of_type("mRNA"):
fid = feat.id
conf_class = feat.attributes.get(gb, "all")
tsize = sum((c.stop - c.start + 1) for c in g.children(fid, 1) \
if c.featuretype == "exon")
print >> fw, "\t".join((fid, str(tsize), conf_class))
fw.close()
tsizes = DictFile(tf, cast=int)
conf_classes = DictFile(tf, valuepos=2)
logging.debug("A total of {0} transcripts populated.".format(len(tsizes)))
genes = []
for feat in g.features_of_type("gene"):
fid = feat.id
transcripts = [c.id for c in g.children(fid, 1) \
if c.featuretype == "mRNA"]
transcript_sizes = [tsizes[x] for x in transcripts]
exons = set((c.chrom, c.start, c.stop) for c in g.children(fid, 2) \
if c.featuretype == "exon")
conf_class = conf_classes[transcripts[0]]
gs = GeneStats(feat, conf_class, transcript_sizes, exons)
genes.append(gs)
r = {} # Report
distinct_groups = set(conf_classes.values())
for g in distinct_groups:
num_genes = num_single_exon_genes = num_multi_exon_genes = 0
num_genes_with_alts = num_transcripts = num_exons = max_transcripts = 0
cum_locus_size = cum_transcript_size = cum_exon_size = 0
for gs in genes:
if gs.conf_class != g:
continue
num_genes += 1
if gs.num_exons == 1:
num_single_exon_genes += 1
else:
num_multi_exon_genes += 1
num_exons += gs.num_exons
if gs.num_transcripts > 1:
num_genes_with_alts += 1
if gs.num_transcripts > max_transcripts:
max_transcripts = gs.num_transcripts
num_transcripts += gs.num_transcripts
cum_locus_size += gs.locus_size
cum_transcript_size += gs.cum_transcript_size
cum_exon_size += gs.cum_exon_size
mean_num_exons = num_exons * 1. / num_genes
mean_num_transcripts = num_transcripts * 1. / num_genes
mean_locus_size = cum_locus_size * 1. / num_genes
mean_transcript_size = cum_transcript_size * 1. / num_transcripts
mean_exon_size = cum_exon_size * 1. / num_exons
r[("Number of genes", g)] = num_genes
r[("Number of single-exon genes", g)] = \
percentage(num_single_exon_genes, num_genes, mode=1)
r[("Number of multi-exon genes", g)] = \
percentage(num_multi_exon_genes, num_genes, mode=1)
r[("Number of distinct exons", g)] = num_exons
r[("Number of genes with alternative transcript variants", g)] = \
percentage(num_genes_with_alts, num_genes, mode=1)
r[("Number of predicted transcripts", g)] = num_transcripts
r[("Mean number of distinct exons per gene", g)] = mean_num_exons
r[("Mean number of transcripts per gene", g)] = mean_num_transcripts
r[("Max number of transcripts per gene", g)] = max_transcripts
r[("Mean gene locus size (first to last exon)", g)] = mean_locus_size
r[("Mean transcript size (UTR, CDS)", g)] = mean_transcript_size
r[("Mean exon size", g)] = mean_exon_size
fw = must_open(opts.outfile, "w")
print >> fw, tabulate(r)
fw.close()
