File: makeflow_gatk_wrapper.xml

package info (click to toggle)
cctools 9.9-2
  • links: PTS, VCS
  • area: main
  • in suites: bookworm
  • size: 44,624 kB
  • sloc: ansic: 192,539; python: 20,827; cpp: 20,199; sh: 11,719; perl: 4,106; xml: 3,688; makefile: 1,224
file content (474 lines) | stat: -rw-r--r-- 25,416 bytes parent folder | download | duplicates (4)
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
367
368
369
370
371
372
373
374
375
376
377
378
379
380
381
382
383
384
385
386
387
388
389
390
391
392
393
394
395
396
397
398
399
400
401
402
403
404
405
406
407
408
409
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
425
426
427
428
429
430
431
432
433
434
435
436
437
438
439
440
441
442
443
444
445
446
447
448
449
450
451
452
453
454
455
456
457
458
459
460
461
462
463
464
465
466
467
468
469
470
471
472
473
474
<tool id="makeflow_gatk" name="Makeflow-GATK" version="1.0.0">
  <description> A Distributed version of GATK using Makeflow</description>
  <requirements>
      <requirement type="package" version="1.4">gatk</requirement>
      <requirement type="package">samtools</requirement>
      <requirement type="package">picard</requirement>
  </requirements>
  <command interpreter="python">
    makeflow_gatk_wrapper.py

    -T $algo

    --input_file=$INPUT

    --reference_sequence=$REFERENCE

    --user_id=$__user_id__
    --pwfile=${GALAXY_DATA_INDEX_DIR}/mypwfile

	--num-seq-part=$numreads

    --out=$VCF_File
    #if $Makeflow_Log:
        --mf_log=$Makeflow_Log
    #end if
    #if $Work_Queue_Log:
        --wq_log=$Work_Queue_Log
    #end if
    #if $Debug_Log:
        --output_dblog=$Debug_Log
    #end if

    #if $checkparams.useparam=="full":
		#if $BQSR:
			--BQSR=$BQSR
		#end if
		#if $EXCLUDE_INTERVALS:
			--excludeIntervals=$EXCLUDE_INTERVALS
		#end if
		#if $INTERVALS:
			--intervals=$$INTERVALS
		#end if
		#if $RG_BLACK_LIST:
			--read_group_black_list=$RG_BLACK_LIST
		#end if


		#if $BAQ:
			--baq=$BAQ
		#end if
		#if $BAQ_GOP:
			--baqGapOpenPenalty=$BAQ_GOP
		#end if
		#if $DEF_BASE_QUALITY:
			--defaultBaseQualities=$DEF_BASE_QUALITY
		#end if
		#if $DOWNSAMPLE_COVERAGE:
			--downsample_to_coverage=$DOWNSAMPLE_COVERAGE
		#end if
		#if $DOWNSAMPLE_FRACTION:
			--downsample_to_fraction=$DOWNSAMPLE_FRACTION
		#end if
		#if $DOWNSAMPLE_TYPE:
			--downsampling_type=$DOWNSAMPLE_TYPE
		#end if
		#if $GATK_KEY:
			--gatk_key=$GATK_KEY
		#end if
		#if $QSCORE_PRIOR:
			--globalQScorePrior=$QSCORE_PRIOR
		#end if
		#if $INTERVAL_MERGING:
			--interval_merging=$INTERVAL_MERGING
		#end if
		#if $INTERVAL_PADDING:
			--interval_padding=$INTERVAL_PADDING
		#end if
		#if $INTERVAL_RULE:
			--interval_set_rule=$INTERVAL_RULE
		#end if
		#if $LOG_LEVEL:
			--logging_level=$LOG_LEVEL
		#end if
		#if $MAX_RUN:
			--maxRuntime=$MAX_RUN
		#end if
		#if $MAX_RUN_UNIT:
			--maxRuntimeUnits=$MAX_RUN_UNIT
		#end if
		#if $CTHREADS_PER_DTHREADS:
			--num_cpu_threads_per_data_thread=$CTHREADS_PER_DTHREADS
		#end if
		#if $NUM_THREADS:
			--num_threads=$NUM_THREADS
		#end if
		#if $PEDIGREE:
			--pedigree=$PEDIGREE
		#end if
		#if $PEDI_STR:
			--pedigreeString=$PEDI_STR
		#end if
		#if $PEDI_VALID:
			--pedigreeValidationType=$PEDI_VALID
		#end if
		#if $ET:
			--phone_home=$ET
		#end if
		#if $PRES_LOW_QSCORE:
			--preserve_qscores_less_than=$PRES_LOW_QSCORE
		#end if
		#if $BUFF_SIZE:
			--read_buffer_size=$BUFF_SIZE
		#end if
		#if $BUFF_FILT:
			--read_filter=$BUFF_FILT
		#end if
		#if $TAG:
			--tag=$TAG
		#end if
		#if $UNSAFE:
			--unsafe=$UNSAFE
		#end if
		#if $VALID_STRICT
			--validation_strictness=$VALID_STRICT
		#end if
		#if $HETER
			--heterozygosity=$HETER
		#end if
		#if $INDEL_HETER
			--indel_heterozygosity=$INDEL_HETER
		#end if


		#if $ALLOW_MISENCOD:
			--allow_potentially_misencoded_quality_scores
		#end if
		#if $DISABLE_INDEL_Q:
			--disable_indel_quals
		#end if
		#if	$EMIT_ORIG:
			--emit_original_quals
		#end if
		#if $FIX_MISENCOD:
			--fix_misencoded_quality_scores
		#end if
		#if	$KEEP_RECORDS:
			--keep_program_records
		#end if
		#if	$MON_THREADS:
			--monitorThreadEfficiency
		#end if
		#if	$RAND_SEED:
			--nonDeterministicRandomSeed
		#end if
		#if	$REMOVE_RECORDS:
			--remove_program_records
		#end if
		#if	$ORIG_QUALS:
			--useOriginalQualities
		#end if
		#if	$VERSION:
			--version
		#end if


		#if	$MAPPING:
			--sample_rename_mapping_file=$MAPPING
		#end if

		#if	$ALLOW_BQSR:
			--allow_bqsr_on_reduced_bams_despite_repeated_warnings
		#end if

    #end if


</command>
<inputs>

	<param format="bam" name="INPUT" type="data" label="Input BAM file" />

	<param format="fasta" name="REFERENCE" type="data"  metadata_name="dbkey" label="Input Reference" />

	<param name="algo" type="select" label="GATK Algorithm">
		<option value="HaplotypeCaller">HaplotypeCaller</option>
    </param>

	<param name="numreads" type="integer" value="10000" label="Number of Sequences per Partition" />

	<conditional name="checkparams">
		<param name="useparam" type="select" label="Other options" help="Select other flags and their values">
			<option value="pre_set">Default settings</option>
			<option value="full">View list</option>
		</param>
		<when value="pre_set" />
		<when value="full">
			<param name="BQSR" type="data" label="BQSR" help="The input covariates table file which enables on-the-fly base quality score recalibration (intended for use with BaseRecalibrator and PrintReads)" />
			<param name="EXCLUDE_INTERVALS" type="data" label="excludeIntervals" help="One or more genomic intervals to exclude from processing. Can be explicitly specified on the command line or in a file (including a rod file)" />
			<param name="INTERVALS" type="data" label="intervals" help="One or more genomic intervals over which to operate. Can be explicitly specified on the command line or in a file (including a rod file)" />
			<param name="RG_BLACK_LIST" type="data" label="read_group_black_list" help="Filters out read groups matching : or a .txt file containing the filter strings one per line." />

			<param name="BAQ" type="text" label="baq" help="Type of BAQ calculation to apply in the engine" />
			<param name="BAQ_GOP" type="text" label="baqGapOpenPenalty" help="BAQ gap open penalty (Phred Scaled). Default value is 40. 30 is perhaps better for whole genome call sets" />
			<param name="DEF_BASE_QUALITY" type="text" label="defaultBaseQualities" help="If reads are missing some or all base quality scores, this value will be used for all base quality scores" />
			<param name="DOWNSAMPLE_COVERAGE" type="text" label="downsample_to_coverage" help="Coverage [integer] to downsample to. For locus-based traversals (eg., LocusWalkers and ActiveRegionWalkers),this controls the maximum depth of coverage at each locus. For non-locus-based traversals (eg., ReadWalkers), this controls the maximum number of reads sharing the same alignment start position. Note that this downsampling option does NOT produce an unbiased random sampling from all available reads at each locus: instead, the primary goal of the to-coverage downsampler is to maintain an even representation of reads from all alignment start positions when removing excess coverage. For a true across-the-board unbiased random sampling of reads, use -dfrac instead. Also note that the coverage target is an approximate goal that is not guaranteed to be met exactly: the downsampling algorithm will under some circumstances retain slightly more coverage than requested." />
			<param name="DOWNSAMPLE_FRACTION" type="text" label="downsample_to_fraction" help="Fraction [0.0-1.0] of reads to downsample to" />
			<param name="DOWNSAMPLE_TYPE" type="text" label="downsampling_type" help="Type of reads downsampling to employ at a given locus. Reads will be selected randomly to be removed from the pile based on the method described here" />
			<param name="GATK_KEY" type="data" label="gatk_key" help="GATK Key file. Required if running with -et NO_ET." />
			<param name="QSCORE_PRIOR" type="text" label="globalQScorePrior" help="The global Qscore Bayesian prior to use in the BQSR. If specified, this value will be used as the prior for all mismatch quality scores instead of the actual reported quality score" />
			<param name="INTERVAL_MERGING" type="text" label="interval_merging" help="Indicates the interval merging rule we should use for abutting intervals" />
			<param name="INTERVAL_PADDING" type="text" label="interval_padding" help="Indicates how many basepairs of padding to include around each of the intervals specified with the -L/--intervals argument" />
			<param name="INTERVAL_RULE" type="text" label="interval_set_rule" help="Indicates the set merging approach the interval parser should use to combine the various -L or -XL inputs" />
			<param name="LOG_LEVEL" type="text" label="logging_level" help="Set the minimum level of logging, i.e. setting INFO get's you INFO up to FATAL, setting ERROR gets you ERROR and FATAL level logging." />
			<param name="MAX_RUN" type="text" label="maxRuntime" help="If provided, that GATK will stop execution cleanly as soon after maxRuntime has been exceeded, truncating the run but not exiting with a failure. By default the value is interpreted in minutes, but this can be changed by maxRuntimeUnits" />
			<param name="MAX_RUN_UNIT" type="text" label="maxRuntimeUnits" help="The TimeUnit for maxRuntime [MINUTES]" />
			<param name="CTHREADS_PER_DTHREADS" type="text" label="num_cpu_threads_per_data_thread" help="How many CPU threads should be allocated per data thread to running this analysis?" />
			<param name="NUM_THREADS" type="text" label="num_threads" help="How many data threads should be allocated to running this analysis." />
			<param name="PEDIGREE" type="data" label="pedigree" help="Pedigree files for samples" />
			<param name="PEDI_STR" type="text" label="pedigreeString" help="Pedigree string for samples" />
			<param name="PEDI_VALID" type="text" label="pedigreeValidationType" help="How strict should we be in validating the pedigree information?" />
			<param name="ET" type="text" label="phone_home" help="What kind of GATK run report should we generate? AWS is the default, can be NO_ET so nothing is posted to the run repository. " />
			<param name="PRES_LOW_QSCORE" type="text" label="preserve_qscores_less_than" help="Bases with quality scores less than this threshold won't be recalibrated (with -BQSR)" />
			<param name="BUFF_SIZE" type="text" label="read_buffer_size" help="Number of reads per SAM file to buffer in memory" />
			<param name="BUFF_FILT" type="text" label="read_filter" help="Specify filtration criteria to apply to each read individually" />
			<param name="TAG" type="text" label="tag" help="Arbitrary tag string to identify this GATK run as part of a group of runs, for later analysis" />
			<param name="VALID_STRICT" type="text" label="validation_strictness" help="How strict should we be with validation" />
			<param name="HETER" type="text" label="heterozygosity" help="Heterozygosity value used to compute prior likelihoods for any locus. See the GATKDocs for full details on the meaning of this population genetics concept" />
			<param name="INDEL_HETER" type="text" label="indel_heterozygosity" help="Heterozygosity for indel calling. See the GATKDocs for heterozygosity for full details on the meaning of this population genetics concept" />

			<param name="UNSAFE" type="boolean" checked="true" label="unsafe" help="If set, enables unsafe operations: nothing will be checked at runtime. For expert users only who know what they are doing. We do not support usage of this argument." />

			<param name="ALLOW_MISENCOD" type="boolean" checked="true" label="allow_potentially_misencoded_quality_scores" help="Do not fail when encountering base qualities that are too high and that seemingly indicate a problem with the base quality encoding of the BAM file" />
			<param name="DISABLE_INDEL_Q" type="boolean" checked="true" label="disable_indel_quals" help="If true, disables printing of base insertion and base deletion tags (with -BQSR)" />
			<param name="EMIT_ORIG" type="boolean" checked="true" label="emit_original_quals" help="If true, enables printing of the OQ tag with the original base qualities (with -BQSR)" />
			<param name="FIX_MISENCOD" type="boolean" checked="true" label="fix_misencoded_quality_scores" help="Fix mis-encoded base quality scores" />
			<param name="KEEP_RECORDS" type="boolean" checked="true" label="keep_program_records" help="Should we override the Walker's default and keep program records from the SAM header" />
			<param name="MON_THREADS" type="boolean" checked="true" label="monitorThreadEfficiency" help="Enable GATK threading efficiency monitoring" />
			<param name="RAND_SEED" type="boolean" checked="true" label="nonDeterministicRandomSeed" help="Makes the GATK behave non deterministically, that is, the random numbers generated will be different in every run" />
			<param name="REMOVE_RECORDS" type="boolean" checked="true" label="remove_program_records" help="Should we override the Walker's default and remove program records from the SAM header" />
			<param name="ORIG_QUALS" type="boolean" checked="true" label="useOriginalQualities" help="If set, use the original base quality scores from the OQ tag when present instead of the standard scores" />
			<param name="VERSION" type="boolean" checked="true" label="version" help="Version Information" />

			<param name="MAPPING" type="data" label="sample_rename_mapping_file" help="Rename sample IDs on-the-fly at runtime using the provided mapping file. This option requires that each BAM file listed in the mapping file have only a single sample specified in its header (though there may be multiple read groups for that sample). Each line of the mapping file must contain the absolute path to a BAM file, followed by whitespace, followed by the new sample name for that BAM file." />

			<param name="ALLOW_BQSR" type="boolean" checked="true" label="allow_bqsr_on_reduced_bams_despite_repeated_warnings" help="Do not fail when running base quality score recalibration on a reduced BAM file even though we highly recommend against it" />
		</when>
	</conditional>

    <param name="log_outputs" type="select" label="Select Optional Outputs" display="checkboxes" multiple="true">
		<option value="OUTPUT_MFLOG">Makeflow Log</option>
		<option value="OUTPUT_WQLOG">Work Queue Log</option>
		<option value="OUTPUT_DBLOG">Debug Log</option>
    </param>
  </inputs>


  <outputs>
    <data format="vcf" name="VCF_File" label="Haplotype-MF VCF File">
      <actions>
        <action type="metadata" name="dbkey">
          <option type="from_param" name="REFERENCE" param_attribute="dbkey" />
        </action>
      </actions>
    </data>
    <data format="mklog" name="Makeflow_Log" label="Haplotype-MF Makeflow Log">
      <filter>"OUTPUT_MFLOG" in log_outputs</filter>
    </data>
    <data format="text" name="Work_Queue_Log" label="Haplotype-MF Work Queue Log">
      <filter>"OUTPUT_WQLOG" in log_outputs</filter>
    </data>
    <data format="text" name="Debug_Log" label="Haplotype-MF Debug Log">
      <filter>"OUTPUT_DBLOG" in log_outputs</filter>
    </data>
  </outputs>
 <help>

  Required Parameters:
    -T TYPE, --analysis_type=TYPE
                        Type of analysis to run

  Optional Inputs:
    --BQSR=BQSR         The input covariates table file which enables on-the-
                        fly base quality score recalibration (intended for use
                        with BaseRecalibrator and PrintReads)
    --excludeIntervals=EXCLUDEINTERVALS
                        One or more genomic intervals to exclude from
                        processing. Can be explicitly specified on the command
                        line or in a file (including a rod file)
    --input_file=INPUT  SAM or BAM file(s)
    --intervals=INTERVALS
                        One or more genomic intervals over which to operate.
                        Can be explicitly specified on the command line or in
                        a file (including a rod file)
    --read_group_black_list=READ_GROUP_BLACK_LIST
                        Filters out read groups matching : or a .txt file
                        containing the filter strings one per line.
    --reference_sequence=REF
                        Reference sequence file
    --reference_index=REF_INDEX
                        Reference sequence file
    --reference_dict=REF_DICT
                        Reference sequence file

  Optional Outputs:
    --log_to_file=LOG   Set the logging location
    --out=OUTPUT        Output name

  Optional Parameters:
    --baq=BAQ           Type of BAQ calculation to apply in the engine
    --baqGapOpenPenalty=BAQGAPOPENPENALTY
                        BAQ gap open penalty (Phred Scaled). Default value is
                        40. 30 is perhaps better for whole genome call sets
    --defaultBaseQualities=DEFAULTBASEQUALITIES
                        If reads are missing some or all base quality scores,
                        this value will be used for all base quality scores
    --downsample_to_coverage=DOWNSAMPLE_TO_COVERAGE
                        Coverage [integer] to downsample to. For locus-based
                        traversals (eg., LocusWalkers and
                        ActiveRegionWalkers),this controls the maximum depth
                        of coverage at each locus. For non-locus-based
                        traversals (eg., ReadWalkers), this controls the
                        maximum number of reads sharing the same alignment
                        start position. Note that this downsampling option
                        does NOT produce an unbiased random sampling from all
                        available reads at each locus: instead, the primary
                        goal of the to-coverage downsampler is to maintain an
                        even representation of reads from all alignment start
                        positions when removing excess coverage. For a true
                        across-the-board unbiased random sampling of reads,
                        use -dfrac instead. Also note that the coverage target
                        is an approximate goal that is not guaranteed to be
                        met exactly: the downsampling algorithm will under
                        some circumstances retain slightly more coverage than
                        requested.
    --downsample_to_fraction=DOWNSAMPLE_TO_FRACTION
                        Fraction [0.0-1.0] of reads to downsample to
    --downsampling_type=DOWNSAMPLING_TYPE
                        Type of reads downsampling to employ at a given locus.
                        Reads will be selected randomly to be removed from the
                        pile based on the method described here
    --gatk_key=GATK_KEY
                        GATK Key file. Required if running with -et NO_ET.
                        Please see
                        http://gatkforums.broadinstitute.org/discussion/1250
                        /what-is-phone-home-and-how-does-it-affect-me#latest
                        for details.
    --globalQScorePrior=GLOBALQSCOREPRIOR
                        The global Qscore Bayesian prior to use in the BQSR.
                        If specified, this value will be used as the prior for
                        all mismatch quality scores instead of the actual
                        reported quality score
    --interval_merging=INTERVAL_MERGING
                        Indicates the interval merging rule we should use for
                        abutting intervals
    --interval_padding=INTERVAL_PADDING
                        Indicates how many basepairs of padding to include
                        around each of the intervals specified with the
                        -L/--intervals argument
    --interval_set_rule=INTERVAL_SET_RULE
                        Indicates the set merging approach the interval parser
                        should use to combine the various -L or -XL inputs
    --logging_level=LOGGING_LEVEL
                        Set the minimum level of logging, i.e. setting INFO
                        get's you INFO up to FATAL, setting ERROR gets you
                        ERROR and FATAL level logging.
    --maxRuntime=MAXRUNTIME
                        If provided, that GATK will stop execution cleanly as
                        soon after maxRuntime has been exceeded, truncating
                        the run but not exiting with a failure. By default the
                        value is interpreted in minutes, but this can be
                        changed by maxRuntimeUnits
    --maxRuntimeUnits=MAXRUNTIMEUNITS
                        The TimeUnit for maxRuntime [MINUTES]
    --num_cpu_threads_per_data_thread=NUM_CPU_THREADS_PER_DATA_THREAD
                        How many CPU threads should be allocated per data
                        thread to running this analysis?
    --num_bam_file_handles=NUM_BAM_FILE_HANDLES
                        The total number of BAM file handles to keep open
                        simultaneously
    --num_threads=NUM_THREADS
                        How many data threads should be allocated to running
                        this analysis.
    --pedigree=PEDIGREE
                        Pedigree files for samples
    --pedigreeString=PEDIGREESTRING
                        Pedigree string for samples
    --pedigreeValidationType=PEDIGREEVALIDATIONTYPE
                        How strict should we be in validating the pedigree
                        information?
    --performanceLog=PLOG
                        If provided, a GATK runtime performance log will be
                        written to this file
    --phone_home=PHONE_HOME
                        What kind of GATK run report should we generate? AWS
                        is the default, can be NO_ET so nothing is posted to
                        the run repository. Please see
                        http://gatkforums.broadinstitute.org/discussion/1250
                        /what-is-phone-home-and-how-does-it-affect-me#latest
                        for details.
    --preserve_qscores_less_than=PRESERVE_QSCORES_LESS_THAN
                        Bases with quality scores less than this threshold
                        won't be recalibrated (with -BQSR)
    --read_buffer_size=READ_BUFFER_SIZE
                        Number of reads per SAM file to buffer in memory
    --read_filter=READ_FILTER
                        Specify filtration criteria to apply to each read
                        individually
    --tag=TAG           Arbitrary tag string to identify this GATK run as part
                        of a group of runs, for later analysis
    --unsafe=UNSAFE     If set, enables unsafe operations: nothing will be
                        checked at runtime. For expert users only who know
                        what they are doing. We do not support usage of this
                        argument.
    --validation_strictness=VALIDATION_STRICTNESS
                        How strict should we be with validation
    --heterozygosity=HETEROZYGOSITY
                        Heterozygosity value used to compute prior likelihoods
                        for any locus. See the GATKDocs for full details on
                        the meaning of this population genetics concept
    --indel_heterozygosity=INDEL_HETEROZYGOSITY
                        Heterozygosity for indel calling. See the GATKDocs for
                        heterozygosity for full details on the meaning of this
                        population genetics concept

  Optional Flags:
    --allow_potentially_misencoded_quality_scores
                        Do not fail when encountering base qualities that are
                        too high and that seemingly indicate a problem with
                        the base quality encoding of the BAM file
    --disable_indel_quals
                        If true, disables printing of base insertion and base
                        deletion tags (with -BQSR)
    --emit_original_quals
                        If true, enables printing of the OQ tag with the
                        original base qualities (with -BQSR)
    --fix_misencoded_quality_scores
                        Fix mis-encoded base quality scores
    --keep_program_records
                        Should we override the Walker's default and keep
                        program records from the SAM header
    --monitorThreadEfficiency
                        Enable GATK threading efficiency monitoring
    --nonDeterministicRandomSeed
                        Makes the GATK behave non deterministically, that is,
                        the random numbers generated will be different in
                        every run
    --remove_program_records
                        Should we override the Walker's default and remove
                        program records from the SAM header
    --useOriginalQualities
                        If set, use the original base quality scores from the
                        OQ tag when present instead of the standard scores
    --version           Output version information

  Advanced Parameters:
    --sample_rename_mapping_file=SAMPLE_RENAME_MAPPING_FILE
                        Rename sample IDs on-the-fly at runtime using the
                        provided mapping file. This option requires that each
                        BAM file listed in the mapping file have only a single
                        sample specified in its header (though there may be
                        multiple read groups for that sample). Each line of
                        the mapping file must contain the absolute path to a
                        BAM file, followed by whitespace, followed by the new
                        sample name for that BAM file.

  Advanced Flags:
    --allow_bqsr_on_reduced_bams_despite_repeated_warnings
                        Do not fail when running base quality score
                        recalibration on a reduced BAM file even though we
                        highly recommend against it


 </help>
</tool>