Mercurial > repos > devteam > freebayes
comparison freebayes.xml @ 15:59731e950e23 draft
Fix some options.
author | soranzo |
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date | Fri, 29 Aug 2014 12:15:44 -0400 |
parents | 2dd40b601766 |
children | 6d9407020066 |
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14:443ccd9208a0 | 15:59731e950e23 |
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117 ${options_type.allele_scope.i} | 117 ${options_type.allele_scope.i} |
118 ${options_type.allele_scope.X} | 118 ${options_type.allele_scope.X} |
119 ${options_type.allele_scope.u} | 119 ${options_type.allele_scope.u} |
120 -n "${options_type.allele_scope.n}" | 120 -n "${options_type.allele_scope.n}" |
121 --haplotype-length "${options_type.allele_scope.haplotype_length}" | 121 --haplotype-length "${options_type.allele_scope.haplotype_length}" |
122 --min-repeat-length "${options_type.allele_scope.min_repeat_length}" | 122 --min-repeat-size "${options_type.allele_scope.min_repeat_length}" |
123 --min-repeat-entropy "${options_type.allele_scope.min_repeat_entropy}" | 123 --min-repeat-entropy "${options_type.allele_scope.min_repeat_entropy}" |
124 ${options_type.allele_scope.no_partial_observations} | 124 ${options_type.allele_scope.no_partial_observations} |
125 #end if | 125 #end if |
126 | 126 |
127 ## REALIGNMENT | 127 ## REALIGNMENT |
164 ## GENOTYPE LIKELIHOODS | 164 ## GENOTYPE LIKELIHOODS |
165 | 165 |
166 #if str( $options_type.genotype_likelihoods.genotype_likelihoods_selector ) == "True": | 166 #if str( $options_type.genotype_likelihoods.genotype_likelihoods_selector ) == "True": |
167 --base-quality-cap "${$options_type.genotype_likelihoods.base_quality_cap}" | 167 --base-quality-cap "${$options_type.genotype_likelihoods.base_quality_cap}" |
168 ${$options_type.genotype_likelihoods.experimental_gls} | 168 ${$options_type.genotype_likelihoods.experimental_gls} |
169 --prob_contamination "${$options_type.genotype_likelihoods.prob_contamination}" | 169 --prob-contamination "${$options_type.genotype_likelihoods.prob_contamination}" |
170 #end if | 170 #end if |
171 | 171 |
172 ## ALGORITHMIC FEATURES | 172 ## ALGORITHMIC FEATURES |
173 | 173 |
174 #if str( $options_type.algorithmic_features.algorithmic_features_selector ) == "True": | 174 #if str( $options_type.algorithmic_features.algorithmic_features_selector ) == "True": |
175 v | 175 ${options_type.algorithmic_features.report_genotype_likelihood_max} |
176 -B "${options_type.algorithmic_features.B}" | 176 -B "${options_type.algorithmic_features.B}" |
177 --genotyping-max-banddepth "${options_type.algorithmic_features.genotyping_max_banddepth}" | 177 --genotyping-max-banddepth "${options_type.algorithmic_features.genotyping_max_banddepth}" |
178 -W "${options_type.algorithmic_features.W}" | 178 -W "${options_type.algorithmic_features.W}" |
179 ${options_type.algorithmic_features.N} | 179 ${options_type.algorithmic_features.N} |
180 | 180 |
373 </conditional> | 373 </conditional> |
374 | 374 |
375 <!-- allelic scope --> | 375 <!-- allelic scope --> |
376 | 376 |
377 <conditional name="allele_scope"> | 377 <conditional name="allele_scope"> |
378 <param name="allele_scope_selector" type="boolean" truevalue="set" falsevalue="do_not_set" label="Set allelic scope?" help="Sets -I, i, -X, -u, -n, -E, --haplotype-length, --min-repeat-length, --min-repeat-entropy, and --no-partial-observations options " /> | 378 <param name="allele_scope_selector" type="boolean" truevalue="set" falsevalue="do_not_set" label="Set allelic scope?" help="Sets -I, i, -X, -u, -n, --haplotype-length, --min-repeat-size, --min-repeat-entropy, and --no-partial-observations options " /> |
379 <when value="set"> | 379 <when value="set"> |
380 <param name="I" type="boolean" truevalue="-I" falsevalue="" checked="False" label="Ignore SNP alleles" help="-I --no-snps; default=False" /> | 380 <param name="I" type="boolean" truevalue="-I" falsevalue="" checked="False" label="Ignore SNP alleles" help="-I --no-snps; default=False" /> |
381 <param name="i" type="boolean" truevalue="-i" falsevalue="" checked="False" label="Ignore indels alleles" help="-i --no-indels; default=False" /> | 381 <param name="i" type="boolean" truevalue="-i" falsevalue="" checked="False" label="Ignore indels alleles" help="-i --no-indels; default=False" /> |
382 <param name="X" type="boolean" truevalue="-X" falsevalue="" checked="False" label="Ignore multi-nucleotide polymorphisms, MNPs" help="-X --no-mnps; default=False" /> | 382 <param name="X" type="boolean" truevalue="-X" falsevalue="" checked="False" label="Ignore multi-nucleotide polymorphisms, MNPs" help="-X --no-mnps; default=False" /> |
383 <param name="u" type="boolean" truevalue="-u" falsevalue="" checked="False" label="Ignore complex events (composites of other classes)." help="-u --no-complex; default=False" /> | 383 <param name="u" type="boolean" truevalue="-u" falsevalue="" checked="False" label="Ignore complex events (composites of other classes)." help="-u --no-complex; default=False" /> |
384 <param name="n" type="integer" value="0" label="How many best SNP alleles to evaluate" help="-n --use-best-n-alleles; default=0 (all). Alleles are ranked by the sum of supporting quality scores. Set to 0 to evaluate all" /> | 384 <param name="n" type="integer" value="0" label="How many best SNP alleles to evaluate" help="-n --use-best-n-alleles; default=0 (all). Alleles are ranked by the sum of supporting quality scores. Set to 0 to evaluate all" /> |
385 <param name="haplotype_length" type="integer" value="3" label="Allow haplotype calls with contiguous embedded matches of up to (nucleotides)" help="--haplotype-length; default=3." /> | 385 <param name="haplotype_length" type="integer" value="3" label="Allow haplotype calls with contiguous embedded matches of up to (nucleotides)" help="-E --max-complex-gap --haplotype-length; default=3." /> |
386 <param name="min_repeat_length" type="integer" value="5" label="When assembling observations across repeats, require the total repeat length at least this many bp" help="--min-repeat-length; default=5." /> | 386 <param name="min_repeat_length" type="integer" value="5" label="When assembling observations across repeats, require the total repeat length at least this many bp" help="--min-repeat-size; default=5." /> |
387 <param name="min_repeat_entropy" type="integer" value="0" label="To detect interrupted repeats, build across sequence until it has entropy > (bits per bp)" help="--min-repeat-entrpy; default=0 (off)." /> | 387 <param name="min_repeat_entropy" type="integer" value="0" label="To detect interrupted repeats, build across sequence until it has entropy > (bits per bp)" help="--min-repeat-entropy; default=0 (off)." /> |
388 <param name="no_partial_observations" type="boolean" truevalue="--no-partial-observations" falsevalue="" checked="False" label="Exclude observations which do not fully span the dynamically-determined detection window" help="--no-partial-observations; default=use all observations, dividing partial support across matching haplotypes when generating haplotypes. " /> | 388 <param name="no_partial_observations" type="boolean" truevalue="--no-partial-observations" falsevalue="" checked="False" label="Exclude observations which do not fully span the dynamically-determined detection window" help="--no-partial-observations; default=use all observations, dividing partial support across matching haplotypes when generating haplotypes. " /> |
389 </when> | 389 </when> |
390 <when value="do_not_set"> | 390 <when value="do_not_set"> |
391 <!-- do nothing --> | 391 <!-- do nothing --> |
392 </when> | 392 </when> |
461 </conditional> | 461 </conditional> |
462 | 462 |
463 <!-- algorithmic features --> | 463 <!-- algorithmic features --> |
464 | 464 |
465 <conditional name="algorithmic_features"> | 465 <conditional name="algorithmic_features"> |
466 <param name="algorithmic_features_selector" type="boolean" truevalue="set" falsevalue="do_not_set" label="Tweak agrithmic features?" help="Sets --report-genotypes-likelihood-max, -B, --genotyping-max-banddepth, -W, -N, S, -j, -H, -D, -= options " /> | 466 <param name="algorithmic_features_selector" type="boolean" truevalue="set" falsevalue="do_not_set" label="Tweak algorithmic features?" help="Sets --report-genotypes-likelihood-max, -B, --genotyping-max-banddepth, -W, -N, S, -j, -H, -D, -= options " /> |
467 <when value="set"> | 467 <when value="set"> |
468 <param name="report_genotype_likelihood_max" type="boolean" truevalue="--report-genotype-likelihood-max" falsevalue="" checked="False" label="Report genotypes using the maximum-likelihood estimate provided from genotype likelihoods." help="--report-genotype-likelihood-max; default=False" /> | 468 <param name="report_genotype_likelihood_max" type="boolean" truevalue="--report-genotype-likelihood-max" falsevalue="" checked="False" label="Report genotypes using the maximum-likelihood estimate provided from genotype likelihoods." help="--report-genotype-likelihood-max; default=False" /> |
469 <param name="B" type="integer" value="1000" label="Iterate no more than N times during genotyping step" help="-B --genotyping-max-iterations; default=1000." /> | 469 <param name="B" type="integer" value="1000" label="Iterate no more than N times during genotyping step" help="-B --genotyping-max-iterations; default=1000." /> |
470 <param name="genotyping_max_banddepth" type="integer" value="6" label="Integrate no deeper than the Nth best genotype by likelihood when genotyping" help="--genotyping-max-banddepth; default=6" /> | 470 <param name="genotyping_max_banddepth" type="integer" value="6" label="Integrate no deeper than the Nth best genotype by likelihood when genotyping" help="--genotyping-max-banddepth; default=6" /> |
471 <param name="W" type="text" size="8" value="1,3" label="Integrate all genotype combinations in our posterior space which include no more than N (1) samples with their Mth (3) best data likelihood" help="-W --posterior-integration-limits; default=1,3" /> | 471 <param name="W" type="text" size="8" value="1,3" label="Integrate all genotype combinations in our posterior space which include no more than N (1) samples with their Mth (3) best data likelihood" help="-W --posterior-integration-limits; default=1,3" /> |
678 supporting quality scores. (Set to 0 to use all; default: all) | 678 supporting quality scores. (Set to 0 to use all; default: all) |
679 -E --max-complex-gap N | 679 -E --max-complex-gap N |
680 --haplotype-length N | 680 --haplotype-length N |
681 Allow haplotype calls with contiguous embedded matches of up | 681 Allow haplotype calls with contiguous embedded matches of up |
682 to this length. (default: 3) | 682 to this length. (default: 3) |
683 --min-repeat-length N | 683 --min-repeat-size N |
684 When assembling observations across repeats, require the total repeat | 684 When assembling observations across repeats, require the total repeat |
685 length at least this many bp. (default: 5) | 685 length at least this many bp. (default: 5) |
686 --min-repeat-entropy N | 686 --min-repeat-entropy N |
687 To detect interrupted repeats, build across sequence until it has | 687 To detect interrupted repeats, build across sequence until it has |
688 entropy > N bits per bp. (default: 0, off) | 688 entropy > N bits per bp. (default: 0, off) |