def check_and_write_data(self, current_lo, bed_file):
if self.gene == None:
return self.trans[0].check_and_write_data(current_lo, bed_file)
# just write the gene if we're a lone gene and it's passed
elif len(self.trans) == 0 and current_lo > self.gene['hi']:
output_row = default_bed_line[:]
output_row[bed_col['chr']] = self.gene['chr']
output_row[bed_col['chr']] = self.gene['lo']
output_row[bed_col['chr']] = self.gene['hi']
output_row[bed_col['chr']] = self.gene['name']
output_row[bed_col['chr']] = self.gene['strand']
if "thick_start" in self.gene:
if self.gene['thick_start'] != dxpy.NULL:
output_row[bed_col['thick_start']] = str(
self.gene['thick_start'])
if "thick_end" in self.gene:
if self.gene['thick_end'] != dxpy.NULL:
output_row[bed_col['thick_end']] = str(
self.gene['thick_end'])
if "score" in self.gene:
if self.gene['score'] != dxpy.NULL:
output_row[bed_col['score']] = str(self.gene['score'])
return True
elif current_lo > self.gene['hi']:
for t in self.trans:
if t.check_and_write_data(current_lo, bed_file) != True:
raise dxpy.AppError(
"found end of gene but not end of transcript: " +
str(self.gene))
return True
else:
return False
def import_BED(**args):
if len(args) == 0:
cmd_line_args = parser.parse_args(sys.argv[1:])
args['filename'] = cmd_line_args.filename
args['reference'] = cmd_line_args.reference
args['file_id'] = cmd_line_args.file_id
args['additional_type'] = cmd_line_args.additional_type
args['property_key'] = cmd_line_args.property_key
args['property_value'] = cmd_line_args.property_value
args['tag'] = cmd_line_args.tag
bed_filename = args['filename']
reference = args['reference']
file_id = args['file_id']
additional_types = args['additional_type']
property_keys = args['property_key']
property_values = args['property_value']
tags = args['tag']
job_outputs = []
# uncompresses file if necessary. Returns new filename
bed_filename_uncomp = unpack( bed_filename )
current_file = 1
for import_filename in split_on_track(bed_filename_uncomp):
try:
bed_basename = os.path.basename(bed_filename)
except:
bed_basename = bed_filename
if current_file == 1:
name = bed_basename
else:
name = bed_basename+"_"+str(current_file)
current_file += 1
bed_type = detect_type(import_filename)["type"]
delimiter = detect_type(import_filename)["delimiter"]
print("Bed type is : " + bed_type, file=sys.stderr)
if bed_type == "genes":
print("Importing as Genes Type", file=sys.stderr)
job_outputs.append(import_genes(import_filename, name, reference, file_id, additional_types, property_keys, property_values, tags, delimiter))
elif bed_type == "spans" or bed_type == "bedDetail":
print("Importing as Spans Type", file=sys.stderr)
if bed_type == "bedDetail":
print("input file is in 'bedDetails' format...", file=sys.stderr)
bedDetail=True
else:
bedDetail=False
job_outputs.append(import_spans(import_filename, name, reference, file_id, additional_types, property_keys, property_values, tags, bedDetail, delimiter))
else:
raise dxpy.AppError("Unable to determine type of BED file")
subprocess.check_call(" ".join(["rm", import_filename]), shell=True)
if(bed_filename != bed_filename_uncomp):
subprocess.check_call(" ".join(["rm", bed_filename_uncomp]), shell=True)
print(json.dumps(job_outputs))
return job_outputs
def RunPindel(kwargs, pindel_command, output_path):
folder = output_path.split("/")[0]
print "Making folder for output: " + str(folder)
os.mkdir(folder)
print "Running pindel with: "
print '\t' + str(pindel_command)
start_time = time.time()
try:
p = subprocess.check_output(pindel_command,
stderr=subprocess.STDOUT,
shell=True)
print p
tot_time = time.time() - start_time
hours = int(tot_time / 3600)
mins = int(float(tot_time % 3600) / 60)
secs = tot_time % 60
print "Pindel ran in: {hrs}h {mins}m {secs}s".format(hrs=hours,
mins=mins,
secs=secs)
except subprocess.CalledProcessError, e:
print "\n" + str(e.output)
raise dxpy.AppError(
"Pindel failed to run. Please check job logs for pindel output. If error is a segmentation fault "
+
"raised as pindel begins to run, check that reference FASTA file is the same reference used to produce the mappings"
)
def ExportVCF(kwargs, output_path, ref_fn):
ref_name_version = dxpy.describe(kwargs["reference_fasta"])["name"]
ref_name_version = ref_name_version.rstrip(".fa")
vcf_out_fn = kwargs["output_prefix"] + '.pindel.vcf'
command_args = ["pindel2vcf"]
command_args.append("-r {input}".format(input=ref_fn))
command_args.append("-P {input}".format(input=output_path))
command_args.append("-v {input}".format(input=vcf_out_fn))
if kwargs["vcf_gatk_compatible"]:
command_args.append("-G")
if "export_vcf_advanced_options" in kwargs:
command_args.append(kwargs["export_vcf_advanced_options"])
else:
ref_date = str(datetime.date.today())
command_args.append("-R {input}".format(input=ref_name_version))
command_args.append("-d ''")
try:
vcf_command = " ".join(command_args)
print "Executing: " + vcf_command
print subprocess.check_output(vcf_command,
stderr=subprocess.STDOUT,
shell=True)
except subprocess.CalledProcessError, e:
print e
print e.output
raise dxpy.AppError(
"APP ERROR: App was not able to convert pindel to vcf. Please check pindel2vcf inputs"
)
def group_files_by_read(fastq_files):
"""
Function : Groups a list of FASTQ files by the values of their Read property that indicates the read number.
Returns a dict mapping each observed value of the property (or 'none' if a file does not have a value
for the property) to a list of the files with that value. Within each group, the files are sorted by their
value of the Chunk property (to ensure that left and right reads of a given chunk are handled together.
Args : fastq_files - a list of dxpy.DXFile objects representing FASTQ files.
Returns : dict.
"""
print("Grouping Fastq files by read number")
read_dict = {}
for fastq_file in fastq_files:
props = fastq_file.get_properties()
read_num = props["read"]
if read_num not in ["1", "2", "none"]:
raise dxpy.AppError("%s has invalid Read property: %s" %
(fastq_file.get_id(), read_num))
if read_num not in read_dict:
read_dict[read_num] = []
read_dict[read_num].append(fastq_file)
#for read_num in read_dict:
# read_dict[read_num] = sorted(read_dict[read_num], key=chunk_property)
return read_dict
def main(**job_inputs):
# If we weren't provided a mmi index for the reference, generate it.
if 'genome_mmi' not in job_inputs:
mmi_input = {'genome_fastagz': job_inputs['genome_fastagz']}
minimap_index_job = dxpy.new_dxjob(mmi_input, 'run_minimap_index')
job_inputs['genome_mmi'] = minimap_index_job.get_output_ref(
'genome_mmi')
output = {'genome_mmi': job_inputs['genome_mmi']}
# check if we're dealing with pacbio or ONT reads and what the filetype is
datatype = job_inputs['datatype']
one_reads_file = dxpy.DXFile(job_inputs['reads'][0]).describe()['name']
try:
file_ext = re.search("(fastq|fasta|fa|fq){1}(.gz)?$",
one_reads_file,
flags=re.I).group(1).lower()
except AttributeError:
raise dxpy.AppError("Invalid filetype extension supplied.")
# for fasta and fastq inputs, run jobs using native minimap2
jobs = run_minimap2_subjobs(job_inputs)
output['bam_files'] = [j.get_output_ref('mapped_reads') for j in jobs]
output['bai_files'] = [
j.get_output_ref('mapped_reads_index') for j in jobs
]
return output
def main(tumor_bams=None, normal_bams=None, cn_reference=None,
baits=None, fasta=None, annotation=None,
method='hybrid', is_male_normal=True, drop_low_coverage=False,
antitarget_avg_size=150000, target_avg_size=267, do_parallel=True):
if not tumor_bams and not normal_bams:
raise dxpy.AppError("Must provide tumor_bams or normal_bams (or both)")
if cn_reference and any((normal_bams, baits, fasta, annotation)):
raise dxpy.AppError("Reference profile (cn_reference) cannot be used "
"alongside normal_bams, baits, fasta, "
"or annotation")
if tumor_bams and not any((baits, cn_reference)):
raise dxpy.AppError("Need cn_reference or baits to process tumor_bams")
print("Downloading file inputs to the local file system")
cn_reference = download_link(cn_reference)
baits = download_link(baits)
fasta = download_link(fasta)
annotation = download_link(annotation)
if tumor_bams is not None:
tumor_bams = map(download_link, tumor_bams)
if normal_bams is not None:
normal_bams = map(download_link, normal_bams)
# If these input files are gzipped, decompress them
fasta = maybe_gunzip(fasta, "ref", "fa")
annotation = maybe_gunzip(annotation, "annot", "txt")
out_fnames = run_cnvkit(tumor_bams, normal_bams, cn_reference, baits,
fasta, annotation, method, is_male_normal,
drop_low_coverage, antitarget_avg_size,
target_avg_size, do_parallel)
print("Uploading local file outputs to the DNAnexus platform")
output = {}
for filekey in ("cn_reference", "seg", "metrics", "genders", "scatter_pdf",
"diagram_pdf"):
if filekey in out_fnames:
output[filekey] = dxpy.dxlink(
dxpy.upload_local_file(out_fnames[filekey]))
for listkey in ("copy_ratios", "copy_segments", "gainloss", "breaks"):
if listkey in out_fnames:
output[listkey] = [dxpy.dxlink(dxpy.upload_local_file(fname))
for fname in out_fnames[listkey]]
return output
def ValidateBamConfig(bam_config_fn, bam_name_array):
print "\nValidating bam config file"
with open(bam_config_fn) as config_fh:
for line in config_fh:
name = line.split()[0]
if name not in bam_name_array:
raise dxpy.AppError(
"Bam config file contains filenames which do not match input bam files"
)
print "\tBam config file is valid"
return True
def main(**job_inputs):
# If we weren't provided a mmi index for the reference, generate it.
if 'genome_mmi' not in job_inputs:
mmi_input = {'genome_fastagz': job_inputs['genome_fastagz']}
minimap_index_job = dxpy.new_dxjob(mmi_input, 'run_minimap_index')
job_inputs['genome_mmi'] = minimap_index_job.get_output_ref(
'genome_mmi')
output = {'genome_mmi': job_inputs['genome_mmi']}
# check if we're dealing with pacbio or ONT reads and what the filetype is
datatype = job_inputs['datatype']
one_reads_file = dxpy.DXFile(job_inputs['reads'][0]).describe()['name']
try:
file_ext = re.search("(bam|fastq|fasta|fa|fq){1}(.gz)?$",
one_reads_file,
flags=re.I).group(1).lower()
except AttributeError:
raise dxpy.AppError("Unknown filetype extension supplied.")
if file_ext == 'bam':
# input bam files must be pacbio raw reads
if datatype == 'ONT':
raise dxpy.AppError("Invalid file input for provided datatype.")
# for bam input, run jobs using pbmm2
jobs = run_pbmm2_subjobs(job_inputs)
else:
# for fasta and fastq inputs, run jobs using native minimap2
if job_inputs['pbbamify']:
print(
'WARNING: The "Run pbbamify" option is only valid for BAM input'
)
jobs = run_minimap2_subjobs(job_inputs)
output['bam_files'] = [j.get_output_ref('mapped_reads') for j in jobs]
output['bai_files'] = [
j.get_output_ref('mapped_reads_index') for j in jobs
]
return output
def check_reads(reads_tables):
# validate that tables contain data that can be used together (all paired or all unpaired, etc)
if len(reads_tables) == 0:
raise dxpy.AppError("Please enter at least one Reads table as input")
single = 0
paired = 0
for table in reads_tables:
if 'sequence2' in dxpy.DXGTable(table).get_col_names():
paired = paired + 1
else:
single = single + 1
if single > 0 and paired > 0:
raise dxpy.AppError(
"Found both single and paired-end reads. Please only input one type."
)
return
def main(**kwargs):
if len(kwargs) == 0:
kwargs = vars(arg_parser.parse_args(sys.argv[1:]))
try:
spans = dxpy.DXGTable(kwargs['Spans'])
except:
raise dxpy.AppError("Failed to open Spans object for export")
spans_types = spans.describe()['types']
if 'Genes' in spans_types:
export_genes(spans, kwargs['output'])
else:
export_generic_bed(spans, kwargs['output'])
def validate_per_tumor(values, n_expected, title, criterion=None):
"""Ensure a per-tumor input array matches the number of tumor BAMs, etc.
Also allow a value of None to skip checks & downstream processing, or a
single value to apply to every tumor sample.
Returns: list of values the same length as `n_expected`.
"""
if values is None:
out_vals = [None] * n_expected
else:
if criterion is not None and not all(map(criterion, values)):
raise dxpy.AppError(
"""Tumor {} must all be between 0 and 1; got: {}""".format(
title, values))
if len(values) == n_expected:
out_vals = values
elif len(values) == 1 and n_expected > 1:
out_vals = [values] * n_expected
else:
raise dxpy.AppError("""Number of tumor {} specified ({}) does not
match the number of tumor BAM files given ({})""".format(
title, len(values), n_expected))
return out_vals
def find_delimiter(bed_file):
with open(bed_file, "rU") as bf:
line = bf.readline()
if line.startswith("track"):
line = bf.readline()
tab_split = line.split("\t")
if len(tab_split) >= 3:
print("Bed file is tab delimited", file=sys.stderr)
return "\t"
else:
space_split = line.split()
if len(space_split) < 3:
raise dxpy.AppError("File is not a valid bed file (neither space delimited nor tab delimited)")
print("Bed file is space delimited", file=sys.stderr)
return " "
def convert_qual(qualString, qual_encode):
convQualString = ''
if qual_encode == 'phred64':
#convert to phred33 do this by subtracting the difference in ASCII offsets
#should be scaling values here? Lose some top end values by doing this
for i in range(len(qualString)):
convQualString += chr(ord(qualString[i]) - 31)
elif qual_encode == 'qual_file':
convQualString = ''.join(
chr(int(i) + 33) for i in qualString.strip(' ').split(' '))
elif qual_encode == 'phred33':
convQualString = qualString
else:
raise dxpy.AppError(
"Unknown quality encoding. Supported encodings are Phred33 and Phred64."
)
return convQualString
def main(**kwargs):
mappings_ids = kwargs["mappings_files"]
mappings_names = sorted([dxpy.describe(id)["name"] for id in mappings_ids])
if "num_threads_per_instance" not in kwargs:
kwargs["num_threads_per_instance"] = multiprocessing.cpu_count()
if "num_instances" not in kwargs:
kwargs["num_instances"] = 1
# Set output prefix here
if "output_prefix" not in kwargs:
kwargs["output_prefix"] = mappings_names[0].rstrip('.bam').rstrip(
'.txt')
# Set output suffixes (for consistency through app)
kwargs["variant_suffixes"] = {
"deletions": 'D',
"short_inserts": 'SI',
"tandem_duplications": 'TD',
"large_inserts": 'LI',
"inversions": 'INV',
"breakpoints": 'BP',
#"breakdancer_outputs": 'BD',
"close_mapped_reads": 'CloseEndMapped'
}
"""
if kwargs["export_vcf"]:
print "\nTESTING pindel2vcf command line inputs on dummy inputs"
ExportVCF(kwargs, output_path="/usr/test_vcf/dummy", ref_fn="/usr/test_vcf/dummy.fa")
"""
# Check if input files have .bam extension
if mappings_names[0][-4:] == ".bam":
for name in mappings_names:
if name[-4:] != ".bam":
raise dxpy.AppError(
"Input mappings files are not all bam files with .bam extensions"
)
app_outputs = RunWithBamInput(kwargs=kwargs)
else:
app_outputs = RunWithPindelInput(kwargs=kwargs, sam2pindel=False)
return app_outputs
def main(sam_file, probability):
# The following line(s) initialize your data object inputs on the platform
# into dxpy.DXDataObject instances that you can start using immediately.
sam_file = dxpy.DXFile(sam_file)
# The following line(s) download your file inputs to the local file system
# using variable names for the filenames.
dxpy.download_dxfile(sam_file.get_id(), "sam_file")
if probability < 0 or probability > 1:
raise dxpy.AppError(
"Probability parameter determines % of mappings included in output. Must be between 0 an 1."
)
subprocess.check_call(" ".join([
"java", "-Xmx2g", "-jar", "/usr/local/bin/DownsampleSam.jar",
"INPUT=sam_file", "OUTPUT=downsampled_sam",
"PROBABILITY=" + str(probability)
]),
shell=True)
# The following line(s) use the Python bindings to upload your file outputs
# after you have created them on the local file system. It assumes that you
# have used the output field name for the filename for each output, but you
# can change that behavior to suit your needs.
downsampled_sam = dxpy.upload_local_file("downsampled_sam")
downsampled_sam.rename(sam_file.describe()['name'] + "_downsampled")
# The following line fills in some basic dummy output and assumes
# that you have created variables to represent your output with
# the same name as your output fields.
output = {}
output["downsampled_sam"] = dxpy.dxlink(downsampled_sam)
return output
def iterate_reads(fastqa1_filename, fastqa2_filename, qual1_filename,
qual2_filename, is_fasta, is_colorspace, qual_encoding):
fastqa1_iter = unpack_and_open(fastqa1_filename).__iter__()
fastqa2_iter, qual1_iter, qual2_iter = None, None, None
if fastqa2_filename != None:
fastqa2_iter = unpack_and_open(fastqa2_filename).__iter__()
if qual1_filename != None:
qual1_iter = unpack_and_open(qual1_filename).__iter__()
if qual2_filename != None:
qual2_iter = unpack_and_open(qual2_filename).__iter__()
read_iter = get_read(fastqa1_iter, qual1_iter, is_fasta, is_colorspace,
qual_encoding).__iter__()
if fastqa1_filename != None:
read_iter2 = get_read(fastqa2_iter, qual2_iter, is_fasta,
is_colorspace, qual_encoding).__iter__()
try:
while True:
temp = read_iter.next()
name1 = temp[0]
seq1 = temp[1]
qual1 = temp[2]
#name1, seq1, qual1 = read_iter.next()
name2, seq2, qual2 = None, None, None
if fastqa2_filename != None:
name2, seq2, qual2 = read_iter2.next()
yield name1, seq1, qual1, name2, seq2, qual2
except StopIteration:
# check to make sure all files we're reading from are all finished at the same time
for file_iter in fastqa1_iter, fastqa2_iter, qual1_iter, qual2_iter:
if file_iter != None:
try:
line = file_iter.next().rstrip("\n")
raise dxpy.AppError(
"Number of reads in each file must be equal")
except StopIteration:
pass
def RunWithPindelInput(kwargs, sam2pindel=False):
pindel_config_fn = "pindel_config.txt"
mappings_names = DownloadFilesFromArray(input_ids=kwargs["mappings_files"])
if sam2pindel:
print "\nInput was not produced by BWA/MOSAIK, running sam2pindel script on input BAM files"
if "sequence_platform" not in kwargs:
raise dxpy.AppError(
"If BAM files were not produced by BWA, must ALSO specify which sequence platform was used to produce the mappings"
)
pindel_config_fn = RunSam2Pindel(
bam_names=mappings_names,
insert_size=kwargs["insert_size"],
seq_platform=kwargs["sequence_platform"],
num_threads=kwargs["num_threads_per_instance"],
config_fn=pindel_config_fn)
else:
print "\nInput is pindel input. Making pindel configuration file"
pindel_config_fn = WriteConfigFile(mappings_names=mappings_names,
fn=pindel_config_fn,
is_pindel=True)
chrom = kwargs["chromosome"] if "chromosome" in kwargs else "ALL"
command, output_path = BuildPindelCommand(kwargs=kwargs,
chrom=chrom,
input_fn=pindel_config_fn,
is_pindel_input_type=True)
output_path = RunPindel(kwargs=kwargs,
pindel_command=command,
output_path=output_path)
app_outputs = UploadPindelOutputs(kwargs=kwargs, output_path=output_path)
if kwargs["export_vcf"]:
app_outputs["vcf"] = ExportVCF(kwargs=kwargs,
output_path=output_path,
ref_fn="reference_fasta")
return app_outputs
def map_contaminant(Contig, Reads):
# get ID of our mapper
try:
bwa = dxpy.DXApp(
dxpy.find_apps(name="bwa_mem_fastq_read_mapper").next()['id'])
except StopIteration:
raise dxpy.AppError(
"Unable to find app 'bwa_mem_fastq_read_mapper'. Please install it to enable contaminant mapping"
)
# TODO: find optimal chunk size so we don't launch too many bwa jobs
map_job = bwa.run({
"reads": Reads,
"reference": Contig,
"discard_unmapped_rows": True,
"chunk_size": 10000000
})
total_reads = 0
for r in Reads:
desc = dxpy.DXGTable(r).describe()
current_reads = desc['length']
if 'sequence2' in desc['columns']:
current_reads *= 2
total_reads += current_reads
# launch a job to wait for the mapping and will calculate what % has mapped
calc_job = dxpy.new_dxjob(
{
"num_reads": total_reads,
"mappings": {
"job": map_job.get_id(),
"field": "mappings"
}
}, "calc_contam")
return calc_job.get_id()
def importGTF(**args):
if len(args) == 0:
command_line_args = parser.parse_args(sys.argv[1:])
fileName = command_line_args.fileName
reference = command_line_args.reference
outputName = command_line_args.outputName
tag = command_line_args.tag
property_key = command_line_args.property_key
property_value = command_line_args.property_value
additional_type = command_line_args.additional_type
file_id = command_line_args.file_id
else:
fileName = args['fileName']
reference = args['reference']
outputName = ''
if args.get('outputName') != None:
outputName = args['outputName']
tag = []
if args.get('tag'):
tag = args['tag']
if args.get('property_key') != None:
property_key = args['property_key']
if args.get('property_value') != None:
property_value = args['property_value']
if args.get('additional_type') != None:
additional_type = args['additional_type']
if args.get('file_id') != None:
file_id = args['file_id']
inputFileName = unpack(fileName)
capturedTypes = {
"5UTR": "5' UTR",
"3UTR": "3' UTR",
"CDS": "CDS",
"inter": "intergenic",
"inter_CNS": "intergenic_conserved",
"intron_CNS": "intron_conserved",
"exon": "exon",
"transcript": "transcript",
"gene": "gene",
"stop_codon": "stop_codon",
"start_codon": "start_codon"
}
#Rows of this type will not be written to the gtable as their information is fully encompassed by the rest of the data
##Isolate the attribute tags from the file and check integrity
spansTable, additionalColumns = constructTable(inputFileName)
spansTable.add_tags(tag)
types = ["Genes", "gri"]
for x in additional_type:
types.append(x)
spansTable.add_types(types)
details = {'original_contigset': dxpy.dxlink(reference)}
if len(property_key) != len(property_value):
raise dxpy.AppError(
"Expected each provided property to have a corresponding value")
for i in range(len(property_key)):
details[property_key[i]] = property_value[i]
for x in additional_type:
types.append(x)
if file_id != None:
details['original_file'] = dxpy.dxlink(file_id)
spansTable.set_details(details)
if outputName == '':
spansTable.rename(fileName)
else:
spansTable.rename(outputName)
#This passes through the file calculates the gene and transcript models
genes = {}
transcripts = {}
spanId = 0
frames = {}
stopCodons = {}
inputFile = open(inputFileName, 'r')
for line in inputFile:
if line[0] != "#":
values = parseLine(line, capturedTypes)
if values["type"] == "CDS":
if frames.get(values["transcriptId"]) == None:
frames[values["transcriptId"]] = {}
frames[values["transcriptId"]][values["lo"]] = values["frame"]
for [element, hashId, elementType
] in [[genes, values["geneId"], "geneName"],
[transcripts, values["transcriptId"],
"transcriptName"]]:
if element.get(hashId) == None:
element[hashId] = {
values["chromosome"]: {
"lo":
values["lo"],
"hi":
values["hi"],
"codingLo":
-1,
"codingHi":
-1,
"strand":
values["strand"],
"score":
values["score"],
"geneId":
values["geneId"],
"coding":
False,
"spanId":
spanId,
"name":
values[elementType],
"originalGeneId":
values["attributes"]["gene_id"],
"originalTranscriptId":
values["attributes"]["transcript_id"]
}
}
spanId += 1
elif element[hashId].get(values["chromosome"]) == None:
element[hashId][values["chromosome"]] = {
"lo":
values["lo"],
"hi":
values["hi"],
"codingLo":
-1,
"codingHi":
-1,
"strand":
values["strand"],
"score":
values["score"],
"geneId":
values["geneId"],
"coding":
False,
"spanId":
spanId,
"name":
values[elementType],
"originalGeneId":
values["attributes"]["gene_id"],
"originalTranscriptId":
values["attributes"]["transcript_id"]
}
spanId += 1
else:
if values["lo"] < element[hashId][
values["chromosome"]]["lo"]:
element[hashId][
values["chromosome"]]["lo"] = values["lo"]
if values["hi"] > element[hashId][
values["chromosome"]]["hi"]:
element[hashId][
values["chromosome"]]["hi"] = values["hi"]
if values["type"] == "stop_codon":
if stopCodons.get(values["transcriptId"]) == None:
stopCodons[values["transcriptId"]] = [[
values["lo"], values["hi"]
]]
else:
stopCodons[values["transcriptId"]].append(
[values["lo"], values["hi"]])
if values["type"] == "CDS" or values[
"type"] == "start_codon" or values["type"] == "stop_codon":
if values["hi"] > transcripts[values["transcriptId"]][
values["chromosome"]]["codingHi"]:
transcripts[values["transcriptId"]][
values["chromosome"]]["codingHi"] = values["hi"]
if values["lo"] < transcripts[values["transcriptId"]][
values["chromosome"]]["codingLo"] or transcripts[
values["transcriptId"]][
values["chromosome"]]["codingLo"] == -1:
transcripts[values["transcriptId"]][
values["chromosome"]]["codingLo"] = values["lo"]
genes[values["geneId"]][values["chromosome"]]["coding"] = True
transcripts[values["transcriptId"]][
values["chromosome"]]["coding"] = True
for gId, chrList in genes.iteritems():
for k, v in chrList.iteritems():
entry = [
k, v["lo"], v["hi"], v["name"], v["spanId"], "gene",
v["strand"], v["score"], v["coding"], -1, -1, '', '',
v["originalGeneId"], ''
]
for x in additionalColumns:
if x != "gene_id" and x != "transcript_id":
entry.append('')
spansTable.add_rows([entry])
for gId, chrList in transcripts.iteritems():
for k, v in chrList.iteritems():
entry = [
k, v["lo"], v["hi"], v["name"], v["spanId"], "transcript",
v["strand"], v["score"], genes[v["geneId"]][k]["coding"],
genes[v["geneId"]][k]["spanId"], -1, '', '',
v["originalGeneId"], v["originalTranscriptId"]
]
for x in additionalColumns:
if x != "gene_id" and x != "transcript_id":
entry.append('')
spansTable.add_rows([entry])
exons = {}
inputFile = open(inputFileName, 'r')
for line in inputFile:
if line[0] != "#":
values = parseLine(line, capturedTypes)
if exons.get(values["transcriptId"]) != None:
if exons[values["transcriptId"]].get(
values["chromosome"]) == None:
exons[values["transcriptId"]][values["chromosome"]] = []
else:
exons[values["transcriptId"]] = {values["chromosome"]: []}
if capturedTypes.get(values["type"]) != None:
#If type is 5'UTR, 3'UTR, intergenic, or conserved intron, type is always noncoding
if values["type"] == "5UTR" or values[
"type"] == "3UTR" or values[
"type"] == "inter" or values[
"type"] == "inter_CNS" or values[
"type"] == "intron_CNS":
writeEntry(
spansTable, spanId, exons[values["transcriptId"]],
additionalColumns, values["chromosome"], values["lo"],
values["hi"], values["attributes"], [
values["chromosome"], values["lo"], values["hi"],
values["name"], spanId,
capturedTypes[values["type"]], values["strand"],
values["score"], False,
transcripts[values["transcriptId"]]["spanId"],
values["frame"], '', values["source"]
])
if "exon_number" in values["attributes"]:
values["transcriptName"] += "." + values["attributes"][
"exon_number"]
#If type is CDS, always of type coding
if values["type"] == "CDS":
if stopCodons.get(values["transcriptId"]) != None:
for x in stopCodons[values["transcriptId"]]:
if values["hi"] == x[0]:
values["hi"] = x[1]
break
if [values["lo"], values["hi"]] not in exons[
values["transcriptId"]][values["chromosome"]]:
spanId = writeEntry(
spansTable, spanId, exons[values["transcriptId"]],
additionalColumns, values["chromosome"],
values["lo"], values["hi"], values["attributes"], [
values["chromosome"], values["lo"],
values["hi"], values["transcriptName"], spanId,
capturedTypes[values["type"]],
values["strand"], values["score"], True,
transcripts[values["transcriptId"]][
values["chromosome"]]["spanId"],
values["frame"], '', values["source"]
])
#If type is exon do calculation as to whether coding or non-coding
if values["type"] == "stop_codon":
values["type"] = "exon"
values["frame"] = 3 - (values["hi"] - values["lo"])
#if values["strand"] == "-":
# values["lo"] = transcripts[values["transcriptId"]][values["chromosome"]]["lo"]
#else:
# values["hi"] = transcripts[values["transcriptId"]][values["chromosome"]]["hi"]
if values["type"] == "exon":
if (transcripts[values["transcriptId"]][
values["chromosome"]]["codingLo"] != -1
and transcripts[values["transcriptId"]][
values["chromosome"]]["codingHi"] != -1):
if frames.get(values["transcriptId"]) != None:
if frames[values["transcriptId"]].get(
values["lo"]) != None:
values["frame"] = frames[
values["transcriptId"]][values["lo"]]
for x in splitExons(
transcripts[values["transcriptId"]],
values["chromosome"], values["lo"],
values["hi"], values["strand"]):
spanId = writeEntry(
spansTable, spanId,
exons[values["transcriptId"]],
additionalColumns, values["chromosome"], x[1],
x[2], values["attributes"], [
values["chromosome"], x[1], x[2],
values["transcriptName"], spanId, x[0],
values["strand"], values["score"], x[3],
transcripts[values["transcriptId"]][
values["chromosome"]]["spanId"],
values["frame"], '', values["source"]
])
else:
spanId = writeEntry(
spansTable, spanId, exons[values["transcriptId"]],
additionalColumns, values["chromosome"],
values["lo"], values["hi"], values["attributes"], [
values["chromosome"], values["lo"],
values["hi"], values["transcriptName"], spanId,
capturedTypes[values["type"]],
values["strand"], values["score"], False,
transcripts[values["transcriptId"]][
values["chromosome"]]["spanId"],
values["frame"], '', values["source"]
])
spansTable.flush()
spansTable.close()
outputFile = open("result.txt", 'w')
outputFile.write(spansTable.get_id())
outputFile.close()
print(spansTable.get_id())
return spansTable.get_id()
def constructTable(inputFileName):
inputFile = open(inputFileName, 'r')
attributes = {"gene_id": True, "transcript_id": True}
for line in inputFile:
if line[0] != "#":
tabSplit = line.split("\t")
if len(tabSplit) == 1:
tabSplit = line.split(" ")
if len(tabSplit) < 9:
raise dxpy.AppError(
"One row did not have 9 entries, it had 1 instead. Offending line: "
+ line)
tabSplit[8] = " ".join(tabSplit[8:])
tabSplit = tabSplit[:9]
if len(tabSplit) != 9:
raise dxpy.AppError("One row did not have 9 entries, it had " +
str(len(tabSplit)) +
" instead. Offending line: " + line)
else:
entrySplit = tabSplit[8].split(";")
geneIdPresent = False
transcriptIdPresent = False
result = []
for x in entrySplit:
keyValue = x.strip().split(" ")
key = keyValue[0]
if key == "gene_id":
geneIdPresent = True
elif key == "transcript_id":
transcriptIdPresent = True
attributes[key] = True
if not geneIdPresent:
raise dxpy.AppError(
"One row did not have a gene_id Offending line: " + line)
if not transcriptIdPresent:
raise dxpy.AppError(
"One row did not have a gene_id Offending line: " + line)
#Construct table
schema = [{
"name": "chr",
"type": "string"
}, {
"name": "lo",
"type": "uint32"
}, {
"name": "hi",
"type": "uint32"
}, {
"name": "name",
"type": "string"
}, {
"name": "span_id",
"type": "int32"
}, {
"name": "type",
"type": "string"
}, {
"name": "strand",
"type": "string"
}, {
"name": "score",
"type": "float"
}, {
"name": "is_coding",
"type": "boolean"
}, {
"name": "parent_id",
"type": "int32"
}, {
"name": "frame",
"type": "int16"
}, {
"name": "description",
"type": "string"
}, {
"name": "source",
"type": "string"
}, {
"name": "gene_id",
"type": "string"
}, {
"name": "transcript_id",
"type": "string"
}]
additionalColumns = ['gene_id', 'transcript_id']
for k, v in attributes.iteritems():
if k != '' and k != 'gene_id' and k != 'transcript_id' and len(
k) < 100:
schema.append({"name": k, "type": "string"})
additionalColumns.append(k)
indices = [
dxpy.DXGTable.genomic_range_index("chr", "lo", "hi", 'gri'),
dxpy.DXGTable.lexicographic_index([
dxpy.DXGTable.lexicographic_index_column("name", True, False),
dxpy.DXGTable.lexicographic_index_column("chr"),
dxpy.DXGTable.lexicographic_index_column("lo"),
dxpy.DXGTable.lexicographic_index_column("hi"),
dxpy.DXGTable.lexicographic_index_column("type")
], "search")
]
spansTable = dxpy.new_dxgtable(columns=schema, indices=indices)
return spansTable, additionalColumns
def parseLine(line, capturedTypes):
tabSplit = line.split("\t")
if len(tabSplit) == 1:
tabSplit = line.split(" ")
if len(tabSplit) < 9:
raise dxpy.AppError(
"One row did not have 9 entries, it had 1 instead. Offending line: "
+ line)
tabSplit[8] = " ".join(tabSplit[8:])
tabSplit = tabSplit[:9]
chromosome = tabSplit[0]
source = tabSplit[1]
typ = tabSplit[2]
if capturedTypes.get(typ) == None:
message = 'Permitted types: ' + " ,".join(capturedTypes.keys())
raise dxpy.AppError(
"One row had a type which is not in the list of permitted types. "
+ message + "\nOffending line: " + line + "\nOffending type: " +
typ)
try:
score = float(tabSplit[5])
except ValueError:
if tabSplit[5] == "." or tabSplit[5] == '':
score = dxpy.NULL
else:
raise dxpy.AppError(
"The score for one line could not be translated into a number and was not \".\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[5])
if tabSplit[6] != "+" and tabSplit[6] != "-" and tabSplit[6] != ".":
raise dxpy.AppError(
"The strand indicated for an element was not \"+\", \"-\", or \".\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[6])
else:
strand = tabSplit[6]
try:
lo = int(tabSplit[3]) - 1
except ValueError:
raise dxpy.AppError(
"One of the start values was could not be translated to an integer. "
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[3])
try:
hi = int(tabSplit[4])
except ValueError:
raise dxpy.AppError(
"One of the start values was could not be translated to an integer. "
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[4])
try:
frame = int(tabSplit[7])
if frame > 2 or frame < 0:
raise dxpy.AppError(
"The frame indicated for an element was not \".\", \"0\", \"1\", or \"2\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[7])
except ValueError:
if tabSplit[7] == ".":
frame = -1
else:
raise dxpy.AppError(
"The frame indicated for an element was not \".\", \"0\", \"1\", or \"2\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[7])
lineAttributes = {}
##Extract the attributes from the file
entrySplit = tabSplit[8].split(";")
result = []
for x in entrySplit:
keyValue = x.strip().split(" ")
key = keyValue[0]
if key != '':
if len(key) < 100:
lineAttributes[key.strip('"')] = keyValue[1].strip('"')
geneId = lineAttributes["gene_id"]
transcriptId = lineAttributes["transcript_id"]
geneName = geneId
if "gene_name" in lineAttributes:
geneName = lineAttributes["gene_name"]
transcriptName = transcriptId
if "transcript_name" in lineAttributes:
transcriptName = lineAttributes["transcript_name"]
values = {
"chromosome": chromosome,
"lo": lo,
"hi": hi,
"geneName": geneName,
"transcriptName": transcriptName,
"source": source,
"type": typ,
"strand": strand,
"score": score,
"frame": frame,
"geneId": geneId,
"transcriptId": transcriptId,
"attributes": lineAttributes
}
return values
def unpack(input):
m = magic.Magic()
# determine compression format
try:
file_type = m.from_file(input)
except Exception as e:
raise dxpy.AppError("Error while identifying compression format: " + str(e))
# if we find a tar file throw a program error telling the user to unpack it
if file_type == 'application/x-tar':
raise dxpy.AppError("App does not support tar files. Please unpack.")
# since we haven't returned, the file is compressed. Determine what program to use to uncompress
uncomp_util = None
if file_type == 'XZ compressed data':
uncomp_util = 'xzcat'
elif file_type[:21] == 'bzip2 compressed data':
uncomp_util = 'bzcat'
elif file_type[:20] == 'gzip compressed data':
uncomp_util = 'zcat'
elif file_type == 'POSIX tar archive (GNU)' or 'tar' in file_type:
raise dxpy.AppError("Found a tar archive. Please untar your sequences before importing")
else:
# just return input filename since it's already uncompressed
return input
if uncomp_util != None:
# bzcat does not support -t. Use non streaming decompressors for testing input
test_util = None
if uncomp_util == 'xzcat':
test_util = 'xz'
elif uncomp_util == 'bzcat':
test_util = 'bzip2'
elif uncomp_util == 'zcat':
test_util = 'gzip'
try:
subprocess.check_call(" ".join([test_util, "-t", input]), shell=True)
except subprocess.CalledProcessError:
raise dxpy.AppError("File failed integrity check by "+uncomp_util+". Compressed file is corrupted.")
# with that in hand, unzip file. If we find a tar archive then exit with error.
try:
with subprocess.Popen([uncomp_util, input], stdout=subprocess.PIPE).stdout as pipe:
line = pipe.next()
uncomp_type = m.from_buffer(line)
except Exception as e:
raise dxpy.AppError("Error detecting file format after decompression: " + str(e))
if uncomp_type == 'POSIX tar archive (GNU)' or 'tar' in uncomp_type:
raise dxpy.AppError("Found a tar archive after decompression. Please untar your files before importing")
elif 'ASCII text' not in uncomp_type:
raise dxpy.AppError("After decompression found file type other than plain text")
try:
out_name = id_generator()
subprocess.check_call(" ".join([uncomp_util, "--stdout", input, ">", out_name]), shell=True)
return out_name
except subprocess.CalledProcessError as e:
raise dxpy.AppError("Unable to open compressed input for reading: " + str(e))
def importGFF(**args):
if len(args) == 0:
args = parser.parse_args(sys.argv[1:])
fileName = args.fileName
reference = args.reference
outputName = args.outputName
file_id = args.file_id
property_key = args.property_key
property_value = args.property_value
tag = args.tag
additional_type = args.additional_type
else:
fileName = args['fileName']
reference = args['reference']
outputName = ''
if args.get('outputName') != None:
outputName = args['outputName']
tag = []
if args.get('tag'):
tag = args['tag']
if args.get('property_key') != None:
property_key = args['property_key']
if args.get('property_value') != None:
property_value = args['property_value']
if args.get('additional_type') != None:
additional_type = args['additional_type']
if args.get('file_id') != None:
file_id = args['file_id']
inputFileName = unpack(fileName)
#Rows of this type will not be written to the gtable as their information is fully encompassed by the rest of the data
discardedTypes = {"start_codon": True, "stop_codon": True}
##Isolate the attribute tags from the file and check integrity
spansTable, additionalColumns = constructTable(inputFileName)
details = {'original_contigset': dxpy.dxlink(reference)}
if file_id != None:
details['original_file'] = dxpy.dxlink(file_id)
if len(property_key) != len(property_value):
raise dxpy.AppError(
"Expected each provided property to have a corresponding value.")
for i in range(len(property_key)):
details[property_key[i]] = property_value[i]
spansTable.set_details(details)
spansTable.add_tags(tag)
if outputName == '':
spansTable.rename(fileName)
else:
spansTable.rename(outputName)
hasGenes = False
#This pass through the file calculates the gene and transcript models
genes = {}
transcripts = {}
spanId = 0
sequenceOntology = {}
for x in [
"five_prime_UTR", "5' UTR", "five prime UTR",
"five_prime_untranslated_region",
"five_prime_coding_exon_noncoding_region",
"five_prime_exon_noncoding_region",
"five prime coding exon noncoding region"
]:
sequenceOntology[x] = "5' UTR"
for x in [
"three_prime_UTR", "3' UTR", "three prime UTR",
"three_prime_untranslated_region",
"three_prime_coding_exon_noncoding_region",
"three_prime_exon_noncoding_region",
"three prime coding exon noncoding region"
]:
sequenceOntology[x] = "3' UTR"
for x in [
"mRNA", "rRNA", "tRNA", "snRNA", "snoRNA", "miRNA", "ncRNA",
"transcript", "mature_transcript",
"rRNA_large_subunit_primary_transcript",
"35S rRNA primary transcript",
"rRNA large subunit primary transcript", "rRNA_primary_transcript",
"enzymatic_RNA", "nc_primary_transcript", "scRNA",
"protein_coding_primary_transcript", "antisense_RNA",
"antisense_primary_transcript", "primary_transcript",
"ribosomal_subunit_rRNA", "small subunit rRNA", "SSU RNA",
"SSU rRNA", "large_subunit_rRNA", "LSU RNA", "LSU rRNA"
]:
sequenceOntology[x] = "transcript"
for x in [
"exon", "interior_coding_exon", "interior coding exon",
"coding_exon", "coding exon", "five_prime_coding_exon_region",
"five prime exon coding region", "three_prime_coding_exon_region",
"three prime coding exon region", "five_prime_coding_exon",
"three_prime_coding_exon", "non_coding_exon", "non coding exon"
]:
sequenceOntology[x] = "exon"
isCoding = {}
for x in [
"CDS", "interior_coding_exon", "interior coding exon",
"coding_exon", "five_prime_coding_exon_region",
"five prime exon coding region", "three_prime_coding_exon_region",
"three prime coding exon region", "five_prime_coding_exon",
"three_prime_coding_exon"
]:
isCoding[x] = True
codingRegions = {}
spans = {}
inputFile = open(inputFileName, 'r')
for line in inputFile:
if line[0] != "#":
values = parseLine(line.split("#")[0])
if values["attributes"].get("Parent") != None:
for parent in values["attributes"]["Parent"].split(","):
if codingRegions.get(parent) == None:
codingRegions[parent] = {
values["chromosome"]: {
"codingLo": -1,
"codingHi": -1
}
}
if isCoding.get(values["type"]) != None:
if values["lo"] < codingRegions[parent][values[
"chromosome"]]["codingLo"] or codingRegions[
parent][values["chromosome"]][
"codingLo"] == -1:
codingRegions[parent][values["chromosome"]][
"codingLo"] = values["lo"]
if values["hi"] > codingRegions[parent][values[
"chromosome"]]["codingHi"] or codingRegions[
parent][values["chromosome"]][
"codingLo"] == -1:
codingRegions[parent][values["chromosome"]][
"codingHi"] = values["hi"]
if values["attributes"].get("ID") != None:
spans[values["attributes"]["ID"]] = spanId
spanId += 1
inputFile = open(inputFileName, 'r')
overflowSpans = spanId
spanId = 0
for line in inputFile:
if line[0] != "#":
values = parseLine(line)
entryIsCoding = False
if isCoding.get(values["type"]) != None:
entryIsCoding = True
if values["attributes"].get("Name") != None:
name = values["attributes"]["Name"]
elif values["attributes"].get("name") != None:
name = values["attributes"]["name"]
elif values["attributes"].get("NAME") != None:
name = values["attributes"]["NAME"]
elif values["attributes"].get("ID") != None:
name = values["attributes"]["ID"]
else:
name = ''
if sequenceOntology.get(values["type"]) != None:
values["type"] = sequenceOntology[values["type"]]
hasGenes = True
description = ''
if values["attributes"].get("description") != None:
description = values["attributes"]["description"]
if values["attributes"].get("Description") != None:
description = values["attributes"]["description"]
parent = -1
if values["type"] not in discardedTypes:
if values["attributes"].get("Parent") != None:
parentSplit = values["attributes"]["Parent"].split(",")
else:
parentSplit = ["-1"]
for parent in parentSplit:
currentSpan = spanId
parentId = -1
if spans.get(parent) != None:
parentId = spans[parent]
if parentSplit.index(parent) > 0:
currentSpan = overflowSpans
overflowSpans += 1
for x in ["ID", "Parent"]:
if not entryIsCoding and values["attributes"].get(
x) != None:
if codingRegions.get(
values["attributes"][x]) != None:
if codingRegions[values["attributes"][x]].get(
"chromosome") != None:
if values["lo"] >= codingRegions[
values["attributes"]
[x]]["chromosome"]["codingLo"] and values[
"lo"] <= codingRegions[
values["attributes"]
[x]]["chromosome"]["codingHi"] and codingRegions[
values["attributes"]
[x]]["chromosome"][
"codingHi"] > -1 and codingRegions[
values["attributes"]
[x]]["chromosome"][
"codingHi"] > -1:
entryIsCoding = True
if values["hi"] >= codingRegions[
values["attributes"]
[x]]["chromosome"]["codingLo"] and values[
"hi"] <= codingRegions[
values["attributes"]
[x]]["chromosome"]["codingHi"] and codingRegions[
values["attributes"]
[x]]["chromosome"][
"codingHi"] > -1 and codingRegions[
values["attributes"]
[x]]["chromosome"][
"codingHi"] > -1:
entryIsCoding = True
entry = [
values["chromosome"], values["lo"], values["hi"], name,
currentSpan, values["type"], values["strand"],
values["score"], entryIsCoding, parentId, values["frame"],
description, values["source"]
]
for x in additionalColumns:
if values["attributes"].get(x) != None:
entry.append(values["attributes"][x])
else:
entry.append('')
spansTable.add_rows([entry])
spanId += 1
if hasGenes:
types = ["Genes", "gri"]
else:
types = ["Spans", "gri"]
for x in additional_type:
types.append(x)
spansTable.add_types(types)
spansTable.flush()
spansTable.close()
print(spansTable.get_id())
job_outputs = dxpy.dxlink(spansTable.get_id())
return job_outputs
def import_spans(bed_file, table_name, ref_id, file_id, additional_types, property_keys, property_values, tags, isBedDetail, delimiter="\t"):
num_cols = find_num_columns(bed_file, delimiter)
# if this is a bedDetail file we should treat the last two columns separately
if isBedDetail:
num_cols -= 2
possible_columns = [("chr", "string"),
("lo", "int32"),
("hi", "int32"),
("name", "string"),
("score", "float"),
("strand", "string"),
("thick_start", "int32"),
("thick_end", "int32"),
("item_rgb", "string")]
bedDetail_columns = [("bedDetail_ID", "string"),
("bedDetail_desc", "string")]
possible_default_row = ["", 0, 0, "", 0, ".", 0, 0, ""]
columns = possible_columns[:num_cols]
if isBedDetail:
columns.extend(bedDetail_columns)
if num_cols > len(columns):
for i in range(len(columns), num_cols):
columns.append(("BED_column_"+str(i+1), "string"))
possible_default_row.append("")
default_row = possible_default_row[:num_cols]
if isBedDetail:
default_row.extend(["",""])
column_descs = [dxpy.DXGTable.make_column_desc(name, type) for name, type in columns]
indices = [dxpy.DXGTable.genomic_range_index("chr","lo","hi", 'gri')]
for c in columns:
if "name" in c:
indices.append(dxpy.DXGTable.lexicographic_index([
dxpy.DXGTable.lexicographic_index_column("name", True, False),
dxpy.DXGTable.lexicographic_index_column("chr"),
dxpy.DXGTable.lexicographic_index_column("lo"),
dxpy.DXGTable.lexicographic_index_column("hi")], "search"))
break
with open(bed_file, 'rU') as bed, dxpy.new_dxgtable(column_descs, indices=indices, mode='w') as span:
details = {"original_contigset": dxpy.dxlink(ref_id)}
if file_id != None:
details["original_file"] = dxpy.dxlink(file_id)
if len(property_keys) != len(property_values):
raise dxpy.AppError("Expected each provided property to have a corresponding value.")
for i in range(len(property_keys)):
details[property_keys[i]] = property_values[i]
span.set_details(details)
span.add_types(["Spans", "gri"])
span.rename(table_name)
for line in bed:
row = list(default_row)
if line.startswith("track"):
details = span.get_details()
details['track'] = line
span.set_details(details)
continue
line = line.rstrip("\n")
line = line.split(delimiter)
if isBedDetail:
# only the first 4 columns are guaranteed to be defined by UCSC
validate_line(line[:4])
# save last two fields separately
bedDetailFields = line[-2:]
line = line[:-2]
else:
validate_line(line[:num_cols])
# check to see if this is a weird line
if len(line) == 0:
break
if len(line) < 3:
raise dxpy.AppError("Line: "+"\t".join(line)+" in BED file contains less than the minimum 3 columns. Invalid BED file.")
try:
row[0] = line[0]
row[1] = int(line[1])
row[2] = int(line[2])
row[3] = line[3]
# dashes are sometimes used when field is invalid
if line[4] == "-" or line[4] == ".":
line[4] = 0
row[4] = float(line[4])
row[5] = line[5]
# dashes are sometimes used when field is invalid
if line[6] == "-" or line[6] == ".":
line[6] = 0
row[6] = int(line[6])
# dashes are sometimes used when field is invalid
if line[7] == "-" or line[7] == ".":
line[7] = 0
row[7] = int(line[7])
row[8] = line[8]
# an index error would come from having fewer columns in a row, which we should handle ok
except IndexError:
pass
# value error when fields are messed up and string gets converted to int, etc. Throw these out.
except ValueError:
continue
if isBedDetail:
# add these in at the end if we have a bedDetail file
row[num_cols] = bedDetailFields[0]
row[num_cols+1] = bedDetailFields[1]
span.add_row(row)
span.flush()
return dxpy.dxlink(span.get_id())
def process(project_id,
output_folder,
fastq_file,
genome_fasta_file,
genome_index_file,
mapper,
mark_duplicates,
fastq_file2=None,
sample_name=None,
properties=None):
"""Download a single FASTQ file, map it, and output a coordinate-sorted
BAM file."""
logger = []
bams_subfolder = output_folder + '/bams'
if mapper not in SUPPORTED_MAPPERS:
raise dxpy.AppError("Unsupported mapper: " + mapper)
if mapper == "bwa_mem":
if fastq_file2 == None:
run_bwa_mem_single(fastq_file, genome_fasta_file,
genome_index_file, mark_duplicates, logger)
else:
run_bwa_mem_paired(fastq_file, fastq_file2, genome_fasta_file,
genome_index_file, mark_duplicates, logger)
elif mapper == "bwa" or mapper == "bwa_aln":
if fastq_file2 == None:
run_bwa_backtrack_single(fastq_file, genome_fasta_file,
genome_index_file, mark_duplicates,
logger)
else:
run_bwa_backtrack_paired(fastq_file, fastq_file2,
genome_fasta_file, genome_index_file,
mark_duplicates, logger)
else:
raise dxpy.AppError("Unsupported mapper: " + mapper)
run_samtools_calmd(logger)
''' From bwa_mem_fastq_read_mapper bash source:
bwa mem -t `nproc` "$genome_file" $input $opts | samtools view -u -S - | samtools sort -m 256M -@ `nproc` - output
samtools index output.bam
'''
index_cmd = 'samtools index sample.bam'
run_cmd(index_cmd, logger)
bam_file = dxpy.upload_local_file(filename="sample.bam",
name=sample_name + ".bam",
properties=properties,
project=project_id,
folder=bams_subfolder,
parents=True)
bai_file = dxpy.upload_local_file(filename="sample.bam.bai",
name=sample_name + ".bai",
properties=properties,
project=project_id,
folder=bams_subfolder,
parents=True)
return {
"bam": dxpy.dxlink(bam_file),
"bai": dxpy.dxlink(bai_file),
"tools_used": logger
}
def import_genes(bed_file, table_name, ref_id, file_id, additional_types, property_keys, property_values, tags, delimiter="\t"):
# implement BED importing from this format:
# http://genome.ucsc.edu/FAQ/FAQformat.html#format1
columns = [("chr", "string"),
("lo", "int32"),
("hi", "int32"),
("name", "string"),
("span_id", "int32"),
("type", "string"),
("strand", "string"),
("is_coding", "boolean"),
("parent_id", "int32"),
("frame", "int16"),
("description", "string")]
column_descs = [dxpy.DXGTable.make_column_desc(name, type) for name, type in columns]
indices = [dxpy.DXGTable.genomic_range_index("chr","lo","hi", 'gri'),
dxpy.DXGTable.lexicographic_index([
dxpy.DXGTable.lexicographic_index_column("name", True, False),
dxpy.DXGTable.lexicographic_index_column("chr"),
dxpy.DXGTable.lexicographic_index_column("lo"),
dxpy.DXGTable.lexicographic_index_column("hi"),
dxpy.DXGTable.lexicographic_index_column("type")], "search")]
default_row = ["", 0, 0, "", -1, "", ".", False, -1, -1, ""]
with open(bed_file, 'rU') as bed, dxpy.new_dxgtable(column_descs, indices=indices, mode='w') as span:
span_table_id = span.get_id()
details = {"original_contigset": dxpy.dxlink(ref_id)}
if file_id != None:
details["original_file"] = dxpy.dxlink(file_id)
if len(property_keys) != len(property_values):
raise dxpy.AppError("Expected each provided property to have a corresponding value.")
for i in range(len(property_keys)):
details[property_keys[i]] = property_values[i]
span.set_details(details)
span.add_types(["gri", "Genes"])
span.rename(table_name)
current_span_id = 0
# where the parsing magic happens
for line in bed:
if line.startswith("track"):
details = span.get_details()
details['track'] = line
span.set_details(details)
continue
line = line.rstrip("\n")
row = list(default_row)
line = line.split(delimiter)
validate_line(line)
if len(line) < 12:
raise dxpy.AppError("Line: "+"\t".join(line)+" in gene model-like BED file contains less than 12 columns. Invalid BED file.")
# add parent gene track
row = generate_gene_row(line, 0, 0, "transcript", default_row, -1, current_span_id)
if row != None:
span.add_row(row)
current_parent_id = current_span_id
current_span_id += 1
# add all children
blockCount = int(line[9])
line[10] = line[10].rstrip(",").split(",")
blockSizes = [int(line[10][n]) for n in range(blockCount)]
line[11] = line[11].rstrip(",").split(",")
blockStarts = [int(line[11][n]) for n in range(blockCount)]
gene_lo = int(line[1])
gene_hi = int(line[2])
# set thick* to be within the gene if outside
thickStart = min(max(int(line[6]), gene_lo), gene_hi)
thickEnd = max(min(int(line[7]), gene_hi), gene_lo)
for i in range(blockCount):
# look to thickStart and thickEnd to get information about the type of this region
# if thick* are the same or cover the whole transcript then we ignore them
# else, we partition the exons into CDS and UTR based on their boundaries
if thickStart == thickEnd or (thickStart == gene_lo and thickEnd == gene_hi):
span.add_row(generate_gene_row(line,
blockSizes[i],
blockStarts[i],
"exon",
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
else:
exon_lo = int(line[1])+blockStarts[i]
exon_hi = int(exon_lo+blockSizes[i])
# we're all UTR if we enter either of these
if (exon_hi <= thickStart and line[5] == '+') or (exon_lo >= thickEnd and line[5] == '-'):
span.add_row(generate_gene_row(line,
blockSizes[i],
blockStarts[i],
"5' UTR",
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
elif (exon_hi <= thickStart and line[5] == '-') or (exon_lo >= thickEnd and line[5] == '+'):
span.add_row(generate_gene_row(line,
blockSizes[i],
blockStarts[i],
"3' UTR",
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
# if this is true then we overlap CDS partially or completely
elif (exon_lo < thickEnd and exon_hi > thickStart):
# entirely contained
if exon_lo >= thickStart and exon_hi <= thickEnd:
span.add_row(generate_gene_row(line,
blockSizes[i],
blockStarts[i],
"CDS",
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
else:
# left portion is UTR
if exon_lo < thickStart:
if line[5] == '+':
UTR_type = "5' UTR"
else:
UTR_type = "3' UTR"
UTR_size = (min(blockSizes[i], thickStart - exon_lo))
span.add_row(generate_gene_row(line,
UTR_size,
blockStarts[i],
UTR_type,
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
# CDS portion
CDS_size = blockSizes[i] - (max(exon_lo, thickStart) - exon_lo)
CDS_size -= (exon_hi - min(exon_hi, thickEnd))
CDS_start = (max(exon_lo, thickStart) - exon_lo) + blockStarts[i]
span.add_row(generate_gene_row(line,
CDS_size,
CDS_start,
"CDS",
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
# right portion is UTR
if exon_hi > thickEnd:
if line[5] == '+':
UTR_type = "3' UTR"
else:
UTR_type = "5' UTR"
UTR_size = (min(blockSizes[i], exon_hi - thickEnd))
UTR_start = blockStarts[i] + thickEnd - exon_lo
span.add_row(generate_gene_row(line,
UTR_size,
UTR_start,
UTR_type,
default_row,
current_parent_id,
current_span_id))
current_span_id += 1
return dxpy.dxlink(span.get_id())
def parseLine(line):
line = line.strip().split("#")[0]
tabSplit = line.split("\t")
if len(tabSplit) == 1:
tabSplit = line.split(" ")
if len(tabSplit) < 8:
raise dxpy.AppError(
"One row did not have 8 or 9 entries, it had 1 instead. Offending line: "
+ line)
tabSplit[8] = " ".join(tabSplit[8:])
tabSplit = tabSplit[:9]
chromosome = tabSplit[0]
source = tabSplit[1]
typ = tabSplit[2]
try:
lo = int(tabSplit[3]) - 1
except ValueError:
raise dxpy.AppError(
"One of the start values was could not be translated to an integer. "
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[3])
try:
hi = int(tabSplit[4])
except ValueError:
raise dxpy.AppError(
"One of the start values was could not be translated to an integer. "
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[4])
try:
score = float(tabSplit[5])
except ValueError:
if tabSplit[5] == "." or tabSplit[5] == '':
score = dxpy.NULL
else:
raise dxpy.AppError(
"The score for one line could not be translated into a number and was not \".\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[5])
tabSplit[6] = tabSplit[6].replace("?", ".")
if tabSplit[6] != "+" and tabSplit[6] != "-" and tabSplit[6] != ".":
raise dxpy.AppError(
"The strand indicated for an element was not \"+\", \"-\", \"?\", or \".\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[6])
else:
strand = tabSplit[6]
try:
frame = int(tabSplit[7])
if frame > 2 or frame < 0:
raise dxpy.AppError(
"The frame indicated for an element was not \".\", \"0\", \"1\", or \"2\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[7])
except ValueError:
if tabSplit[7] == ".":
frame = -1
else:
raise dxpy.AppError(
"The frame indicated for an element was not \".\", \"0\", \"1\", or \"2\""
+ "\nOffending line: " + line + "\nOffending value: " +
tabSplit[7])
lineAttributes = {}
##Extract the attributes from the file
if len(tabSplit) >= 9:
reg = re.findall("([^=]*)=([^;]*);", tabSplit[8].strip() + ";")
for x in reg:
if len(x[0]) < 100:
lineAttributes[x[0]] = x[1].strip().strip("\"")
else:
lineAttributes = {}
values = {
"chromosome": chromosome,
"lo": lo,
"hi": hi,
"source": source,
"type": typ,
"strand": strand,
"score": score,
"frame": frame,
"attributes": lineAttributes
}
return values
def validate_line(line):
line_str = "\t".join(line)
entries = list(line)
if len(entries) > 1:
try:
if int(entries[1]) < 0:
raise dxpy.AppError("The start position for one entry was unexpectedly negative. \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[1]))
except ValueError:
raise dxpy.AppError("One of the start values could not be translated to an integer. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[1]))
if len(entries) > 2:
try:
if int(entries[2]) < 0:
raise dxpy.AppError("The end position for one entry was unexpectedly negative. \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[2]))
except ValueError:
raise dxpy.AppError("One of the end values could not be translated to an integer. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[2]))
if len(entries) > 4:
try:
if entries[4] != "." and entries[4] != "-":
float(entries[4])
except ValueError:
raise dxpy.AppError("One of the score values for one entry could not be translated to a number. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[4]))
if len(entries) > 5:
if entries[5] != "+" and entries[5] != "-" and entries[5] != ".":
raise dxpy.AppError("The strand indicated for an element was not \"+\", \"-\", or \".\"" + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[5]))
if len(entries) > 6:
try:
if entries[6] != "." and entries[6] != "-":
if int(entries[6]) < 0:
raise dxpy.AppError("The thickStart position for one entry was unexpectedly negative. \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[6]))
except ValueError:
raise dxpy.AppError("One of the thickStart values could not be translated to an integer. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[6]))
if len(entries) > 7:
try:
if entries[7] != "." and entries[7] != "-":
if int(entries[7]) < 0:
raise dxpy.AppError("The thickEnd position for one entry was unexpectedly negative. \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[7]))
except ValueError:
raise dxpy.AppError("One of the thickEnd values could not be translated to an integer. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[7]))
if len(entries) > 9:
try:
if int(entries[9]) < 0:
raise dxpy.AppError("The number of exons (blockCount) for one entry was unexpectedly negative. \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[9]))
except ValueError:
raise dxpy.AppError("One of the thickEnd values could not be translated to an integer. " + "\nOffending line_str: " + line_str + "\nOffending value: " + str(entries[9]))
if len(entries) > 10:
try:
entries[10] = entries[10].rstrip(",").split(",")
blockStarts = [int(entries[10][n]) for n in range(int(entries[9]))]
except:
raise dxpy.AppError("Could not parse the blockSizes entry as a comma-separated list of integers \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[10]))
if len(entries) > 11:
try:
entries[11] = entries[11].rstrip(",").split(",")
blockStarts = [int(entries[11][n]) for n in range(int(entries[9]))]
except:
raise dxpy.AppError("Could not parse the blockStarts entry as a comma-separated list of integers \nOffending line_str: " + line_str + "\nOffending value: " + str(entries[11]))
def constructTable(inputFileName):
inputFile = open(inputFileName, 'r')
attributes = {}
for line in inputFile:
if line[0] != "#":
line = line.strip().split("#")[0]
tabSplit = line.split("\t")
if len(tabSplit) == 1:
tabSplit = line.split(" ")
if len(tabSplit) < 9:
raise dxpy.AppError(
"One row did not have 8 or 9 entries, it had 1 instead. Offending line: "
+ line)
tabSplit[8] = " ".join(tabSplit[8:])
tabSplit = tabSplit[:9]
if len(tabSplit) != 8 and len(tabSplit) != 9:
raise dxpy.AppError(
"One row did not have 8 or 9 entries, it had " +
str(len(tabSplit)) + " instead. Offending line: " + line)
elif len(tabSplit) == 9:
reg = re.findall("([^=]*)=([^;]*);", tabSplit[8].strip() + ";")
for x in reg:
attributes[x[0]] = True
reservedColumns = [
"", "chr", "lo", "hi", "name", "span_id", "type", "score", "is_coding",
"parent_id", "frame", "description", "source"
]
#Construct table
schema = [{
"name": "chr",
"type": "string"
}, {
"name": "lo",
"type": "uint32"
}, {
"name": "hi",
"type": "uint32"
}, {
"name": "name",
"type": "string"
}, {
"name": "span_id",
"type": "int32"
}, {
"name": "type",
"type": "string"
}, {
"name": "strand",
"type": "string"
}, {
"name": "score",
"type": "float"
}, {
"name": "is_coding",
"type": "boolean"
}, {
"name": "parent_id",
"type": "int32"
}, {
"name": "frame",
"type": "int16"
}, {
"name": "description",
"type": "string"
}, {
"name": "source",
"type": "string"
}]
additionalColumns = []
for k, v in attributes.iteritems():
if k not in reservedColumns and len(k) < 100:
schema.append({"name": k, "type": "string"})
additionalColumns.append(k)
indices = [
dxpy.DXGTable.genomic_range_index("chr", "lo", "hi", 'gri'),
dxpy.DXGTable.lexicographic_index([
dxpy.DXGTable.lexicographic_index_column("name", True, False),
dxpy.DXGTable.lexicographic_index_column("chr"),
dxpy.DXGTable.lexicographic_index_column("lo"),
dxpy.DXGTable.lexicographic_index_column("hi"),
dxpy.DXGTable.lexicographic_index_column("type")
], "search")
]
spansTable = dxpy.new_dxgtable(columns=schema, indices=indices)
return spansTable, additionalColumns