예제 #1
0
파일: sort.py 프로젝트: MarcSaric/maf-lib
 def __add_arguments__(cls, subparser):
     """
     Add arguments to a subparser.
     """
     sort_orders = [c.name() for c in SortOrder.all()]
     subparser.add_argument('-i',
                            '--input',
                            dest='input',
                            required=True,
                            help='A MAF file.')
     subparser.add_argument('-o',
                            '--output',
                            default=None,
                            help="The output file, otherwise output will be"
                            " to standard output.")
     subparser.add_argument('-s',
                            '--sort-order',
                            default=BarcodesAndCoordinate.name(),
                            choices=sort_orders,
                            help="The sort order to choose.  "
                            "Choices: %s" % ", ".join(sort_orders))
     subparser.add_argument('-f',
                            '--fasta-index',
                            default=None,
                            help="Use the FASTA index (fai) to order "
                            "genomic coordinates.")
예제 #2
0
    def test_sorter_with_sort_order_args(self):
        lines = [
            "chr1\t248956422\t112\t70\t71"
            "chr2\t242193529\t252513167\t70\t71",
            "chr3\t198295559\t498166716\t70\t71",
            "chr4\t190214555\t699295181\t70\t71",
            "chr5\t181538259\t892227221\t70\t71",
            "chr6\t170805979\t1076358996\t70\t71",
            "chr7\t159345973\t1249605173\t70\t71",
            "chr8\t145138636\t1411227630\t70\t71",
            "chr9\t138394717\t1558439788\t70\t71",
            "chr10\t133797422\t1698811686\t70\t71",
        ]
        fd, fn = tmp_file(lines=lines)

        sorter = MafSorter(
            sort_order_name=BarcodesAndCoordinate.name(),
            max_objects_in_ram=100,
            fasta_index=fn,
        )

        self.__test_sorter(sorter=sorter, chromosome="chr5")

        with self.assertRaises(ValueError):
            self.__test_sorter(sorter=sorter, chromosome="1")

        fd.close()
        os.remove(fn)
예제 #3
0
    def test_end_to_end(self):
        lines, header, records = self.read_test_maf()

        # reverse the lines
        input_lines = header + list(reversed(records))
        subcommand_args = [
            "--version",
            GdcV1_0_0_PublicScheme.version(), "--annotation",
            GdcV1_0_0_PublicScheme.annotation_spec()
        ]
        out_lines, stdout, stderr = run_main(subcommand="sort",
                                             lines=input_lines,
                                             subcommand_args=subcommand_args)
        out_records = [line for line in out_lines if not line.startswith("#")]

        # Check that we have the same # of records
        out_records = [line for line in out_lines \
                       if not line.startswith("#") and not line.startswith("Hugo_Symbol")]
        self.assertEqual(len(out_records), len(records))

        # Check that we added the sort pragma
        sortOrderLine = "%s%s %s" % (MafHeader.HeaderLineStartSymbol,
                                     MafHeader.SortOrderKey,
                                     BarcodesAndCoordinate.name())
        self.assertTrue(sortOrderLine in out_lines)

        self.assertEqual(len(out_lines) - 1, len(lines))  # added the pragma
예제 #4
0
 def test_sorter_with_scheme(self):
     scheme = DummyScheme()
     sorter = MafSorter(
         sort_order_name=BarcodesAndCoordinate.name(),
         scheme=scheme,
         max_objects_in_ram=100,
     )
     self.__test_sorter(sorter=sorter, with_scheme=True)
예제 #5
0
    def test_with_fasta_index(self):
        # change the order of chromosomes!
        fasta_index_lines = [
            "chr13\t114364328\t2106716512\t70\t71",
            "chr1\t248956422\t112\t70\t71"
        ]
        fd, fn = tmp_file(lines=fasta_index_lines)
        lines, header, records = self.read_test_maf()
        subcommand_args = [
            "--version",
            GdcV1_0_0_PublicScheme.version(), "--annotation",
            GdcV1_0_0_PublicScheme.annotation_spec()
        ]
        out_lines, stdout, stderr = run_main(subcommand="sort",
                                             lines=lines,
                                             subcommand_args=subcommand_args)

        # Check that we have the same # of records
        out_records = [line for line in out_lines \
                       if not line.startswith("#") and not line.startswith("Hugo_Symbol")]
        self.assertEqual(len(out_records), len(records))

        # Check that we added the sort pragma
        sortOrderLine = "%s%s %s" % (MafHeader.HeaderLineStartSymbol,
                                     MafHeader.SortOrderKey,
                                     BarcodesAndCoordinate.name())
        self.assertTrue(sortOrderLine in out_lines)

        scheme = find_scheme(
            version=GdcV1_0_0_PublicScheme.version(),
            annotation=GdcV1_0_0_PublicScheme.annotation_spec())
        # we should see chr13 before chr1
        self.assertEqual(len(out_lines) - 1, len(lines))  # added the pragma
        found_chr1 = False
        for line in out_lines:
            if line.startswith(MafHeader.HeaderLineStartSymbol):
                continue
            record = MafRecord.from_line(line=line, scheme=scheme)
            self.assertFalse(record["Chromosome"] == "chr13" and found_chr1)
            found_chr1 = record["Chromosome"] == "chr1"
        fd.close()
        os.remove(fn)
    def do_work(self):
        """Main wrapper function for running protect MAF merging"""

        # Reader
        self.load_readers()

        # Header
        self.setup_maf_header()

        self._scheme = self.maf_header.scheme()
        self._columns = get_columns_from_header(self.maf_header)

        # Sorter
        sorter = MafSorter(max_objects_in_ram=100000,
                           sort_order_name=BarcodesAndCoordinate.name(),
                           scheme=self.maf_header.scheme(),
                           contigs=self.maf_header.contigs())

        # Merger
        self._merger = MafRecordMerger_1_0_0(self._scheme)

        # Overlap iterator
        o_iter = LocatableOverlapIterator(
            self.maf_readers,
            contigs=self.maf_header.contigs(),
            peekable_iterator_class=FilteringPeekableIterator)

        # ndp filter
        ndp_filter = Filters.NormalDepth.setup(self.options['min_n_depth'])
        ndp_tag = ndp_filter.tags[0]

        # Counts
        processed = 0
        try:
            for record in o_iter:

                if processed > 0 and processed % 1000 == 0:
                    self.logger.info(
                        "Processed {0} overlapping intervals...".format(
                            processed))

                result = OverlapSet(record, self.callers)

                for maf_record in self._merger.merge_records(result):
                    if maf_record is not None:
                        # Recheck normal depth
                        gdc_filters = maf_record['GDC_FILTER'].value
                        has_tag = ndp_tag in gdc_filters
                        ndp = ndp_filter.filter(maf_record)
                        if has_tag != ndp:
                            if ndp:
                                gdc_filters.extend(ndp_filter.tags)
                            else:
                                gdc_filters = list(
                                    filter(lambda x: x != ndp_filter.tags[0],
                                           gdc_filters))

                            maf_record["GDC_FILTER"] = get_builder(
                                "GDC_FILTER",
                                self._scheme,
                                value=sorted(gdc_filters))

                        # Add to sorter
                        sorter += maf_record

                processed += 1

            self.logger.info(
                "Writing {0} sorted, merged records...".format(processed))

            # Writer
            self.maf_writer = MafWriter.from_path(
                path=self.options['output_maf'],
                header=self.maf_header,
                validation_stringency=ValidationStringency.Strict)

            counter = 0
            for record in sorter:
                if counter > 0 and counter % 1000 == 0:
                    self.logger.info(
                        "Wrote {0} sorted, merged records...".format(counter))
                self.maf_writer += record
                counter += 1

            self.logger.info(
                "Finished writing {0} sorted, merged records.".format(counter))

        finally:
            for reader in self.maf_readers:
                reader.close()

            sorter.close()

            if self.maf_writer:
                self.maf_writer.close()
    def do_work(self):
        """Main wrapper function for running vcf2maf"""
        self.logger.info(
            "Processing input vcf {0}...".format(self.options["input_vcf"])
        )

        # Initialize the maf file
        self.setup_maf_header()

        sorter = MafSorter(
            max_objects_in_ram=100000,
            sort_order_name=BarcodesAndCoordinate.name(),
            scheme=self.maf_header.scheme(),
            fasta_index=self.options["reference_fasta_index"],
        )

        self._scheme = self.maf_header.scheme()
        self._columns = get_columns_from_header(self.maf_header)
        self._colset = set(self._columns)

        # Initialize vcf reader
        vcf_object = pysam.VariantFile(self.options["input_vcf"])
        tumor_sample_id = self.options["tumor_vcf_id"]
        normal_sample_id = self.options["normal_vcf_id"]
        is_tumor_only = self.options["tumor_only"]

        try:
            # Validate samples
            tumor_idx = assert_sample_in_header(
                vcf_object, self.options["tumor_vcf_id"]
            )
            normal_idx = assert_sample_in_header(
                vcf_object, self.options["normal_vcf_id"], can_fail=is_tumor_only
            )

            # extract annotation from header
            ann_cols_format, vep_key = extract_annotation_from_header(
                vcf_object, vep_key="CSQ"
            )

            # Initialize annotators
            self.setup_annotators()

            # Initialize filters
            self.setup_filters()

            # Convert
            line = 0
            for vcf_record in vcf_object.fetch():

                line += 1

                if line % 1000 == 0:
                    self.logger.info("Processed {0} records...".format(line))

                # Extract data
                data = self.extract(
                    tumor_sample_id,
                    normal_sample_id,
                    tumor_idx,
                    normal_idx,
                    ann_cols_format,
                    vep_key,
                    vcf_record,
                    is_tumor_only,
                )

                # Skip rare occasions where VEP doesn't provide IMPACT or the consequence is ?
                if (
                    not data["selected_effect"]["IMPACT"]
                    or data["selected_effect"]["One_Consequence"] == "?"
                ):
                    self.logger.warn(
                        "Skipping record with unknown impact or consequence: {0} - {1}".format(
                            data["selected_effect"]["IMPACT"],
                            data["selected_effect"]["One_Consequence"],
                        )
                    )
                    continue

                # Transform
                maf_record = self.transform(
                    vcf_record, data, is_tumor_only, line_number=line
                )

                # Add to sorter
                sorter += maf_record

            # Write
            self.logger.info("Writing {0} sorted records...".format(line))
            self.maf_writer = MafWriter.from_path(
                path=self.options["output_maf"],
                header=self.maf_header,
                validation_stringency=ValidationStringency.Strict,
            )

            counter = 0
            for record in sorter:

                counter += 1

                if counter % 1000 == 0:
                    self.logger.info("Wrote {0} records...".format(counter))

                self.maf_writer += record

            self.logger.info("Finished writing {0} records".format(counter))

        finally:
            vcf_object.close()
            sorter.close()
            if self.maf_writer:
                self.maf_writer.close()
            for anno in self.annotators:
                if self.annotators[anno]:
                    self.annotators[anno].shutdown()

        self.logger.info("Finished")
예제 #8
0
 def test_sorter_default(self):
     sorter = MafSorter(sort_order_name=BarcodesAndCoordinate.name(),
                        max_objects_in_ram=100)
     self.__test_sorter(sorter=sorter)