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/tools/sr_mapping/bowtie_wrapper.xml

https://bitbucket.org/cistrome/cistrome-harvard/
XML | 838 lines | 766 code | 34 blank | 38 comment | 0 complexity | 449552858fd209f2ed4301bc29f8b742 MD5 | raw file
  1. <tool id="bowtie_wrapper" name="Map with Bowtie for Illumina" version="1.1.2">
  2. <requirements><requirement type='package'>bowtie</requirement></requirements>
  3. <description></description>
  4. <parallelism method="basic"></parallelism>
  5. <command interpreter="python">
  6. bowtie_wrapper.py
  7. ## Hackish setting of number of threads
  8. --threads="4"
  9. ## Outputs
  10. --output=$output
  11. #if str( $singlePaired.sPaired ) == "single"
  12. #if $output_unmapped_reads_l
  13. --output_unmapped_reads=$output_unmapped_reads_l
  14. #end if
  15. #if $output_suppressed_reads_l
  16. --output_suppressed_reads=$output_suppressed_reads_l
  17. #end if
  18. --galaxy_input_format="${singlePaired.sInput1.ext}"
  19. #else
  20. #if $output_unmapped_reads_l and $output_unmapped_reads_r
  21. --output_unmapped_reads_l=$output_unmapped_reads_l
  22. --output_unmapped_reads_r=$output_unmapped_reads_r
  23. #end if
  24. #if $output_suppressed_reads_l and $output_suppressed_reads_l
  25. --output_suppressed_reads_l=$output_suppressed_reads_l
  26. --output_suppressed_reads_r=$output_suppressed_reads_r
  27. #end if
  28. --galaxy_input_format="${singlePaired.pInput1.ext}"
  29. #end if
  30. ## Inputs
  31. --dataType="solexa" ##this indicates that nucleotide base space is used in the wrapper
  32. --suppressHeader=$suppressHeader
  33. --genomeSource=$refGenomeSource.genomeSource
  34. #if $refGenomeSource.genomeSource == "history":
  35. ##index already exists
  36. #if $refGenomeSource.ownFile.extension.startswith( 'bowtie_' ):
  37. ##user previously built
  38. --ref="${refGenomeSource.ownFile.extra_files_path}/${refGenomeSource.ownFile.metadata.base_name}"
  39. --do_not_build_index
  40. #else:
  41. ##build index on the fly
  42. --ref=$refGenomeSource.ownFile
  43. --indexSettings=$refGenomeSource.indexParams.indexSettings
  44. #if $refGenomeSource.indexParams.indexSettings == "indexFull":
  45. --iautoB=$refGenomeSource.indexParams.autoBehavior.autoB
  46. #if $refGenomeSource.indexParams.autoBehavior.autoB == "set":
  47. --ipacked=$refGenomeSource.indexParams.autoBehavior.packed
  48. --ibmax=$refGenomeSource.indexParams.autoBehavior.bmax
  49. --ibmaxdivn=$refGenomeSource.indexParams.autoBehavior.bmaxdivn
  50. --idcv=$refGenomeSource.indexParams.autoBehavior.dcv
  51. #end if
  52. --inodc=$refGenomeSource.indexParams.nodc
  53. --inoref=$refGenomeSource.indexParams.noref
  54. --ioffrate=$refGenomeSource.indexParams.offrate
  55. --iftab=$refGenomeSource.indexParams.ftab
  56. --intoa=$refGenomeSource.indexParams.ntoa
  57. --iendian=$refGenomeSource.indexParams.endian
  58. --iseed=$refGenomeSource.indexParams.seed
  59. --icutoff=$refGenomeSource.indexParams.cutoff
  60. #end if
  61. #end if
  62. #else
  63. ##use pre-built index
  64. ##--ref="${ filter( lambda x: str( x[0] ) == str( $refGenomeSource.index ), $__app__.tool_data_tables[ 'bowtie_indexes' ].get_fields() )[0][-1] }"
  65. --ref="${ refGenomeSource.index.fields.path }"
  66. #end if
  67. --paired=$singlePaired.sPaired
  68. #if $singlePaired.sPaired == "single":
  69. --input1=$singlePaired.sInput1
  70. --params=$singlePaired.sParams.sSettingsType
  71. #if $singlePaired.sParams.sSettingsType == "full":
  72. --skip=$singlePaired.sParams.sSkip
  73. --alignLimit=$singlePaired.sParams.sAlignLimit
  74. --trimH=$singlePaired.sParams.sTrimH
  75. --trimL=$singlePaired.sParams.sTrimL
  76. --mismatchSeed=$singlePaired.sParams.sMismatchSeed
  77. --mismatchQual=$singlePaired.sParams.sMismatchQual
  78. --seedLen=$singlePaired.sParams.sSeedLen
  79. --rounding=$singlePaired.sParams.sRounding
  80. --maqSoapAlign=$singlePaired.sParams.sMaqSoapAlign
  81. --tryHard=$singlePaired.sParams.sTryHard
  82. --valAlign=$singlePaired.sParams.sValAlign
  83. --allValAligns=$singlePaired.sParams.sAllValAligns
  84. --suppressAlign=$singlePaired.sParams.sSuppressAlign
  85. --best=$singlePaired.sParams.sBestOption.sBest
  86. #if $singlePaired.sParams.sBestOption.sBest == "doBest":
  87. --maxBacktracks=$singlePaired.sParams.sBestOption.sdMaxBacktracks
  88. --strata=$singlePaired.sParams.sBestOption.sdStrata
  89. #else:
  90. --maxBacktracks=$singlePaired.sParams.sBestOption.snMaxBacktracks
  91. #end if
  92. --offrate=$singlePaired.sParams.sOffrate
  93. --seed=$singlePaired.sParams.sSeed
  94. #end if
  95. #else:
  96. --input1=$singlePaired.pInput1
  97. --input2=$singlePaired.pInput2
  98. --maxInsert=$singlePaired.pMaxInsert
  99. --mateOrient=$singlePaired.pMateOrient
  100. --params=$singlePaired.pParams.pSettingsType
  101. #if $singlePaired.pParams.pSettingsType == "full":
  102. --skip=$singlePaired.pParams.pSkip
  103. --alignLimit=$singlePaired.pParams.pAlignLimit
  104. --trimH=$singlePaired.pParams.pTrimH
  105. --trimL=$singlePaired.pParams.pTrimL
  106. --mismatchSeed=$singlePaired.pParams.pMismatchSeed
  107. --mismatchQual=$singlePaired.pParams.pMismatchQual
  108. --seedLen=$singlePaired.pParams.pSeedLen
  109. --rounding=$singlePaired.pParams.pRounding
  110. --maqSoapAlign=$singlePaired.pParams.pMaqSoapAlign
  111. --minInsert=$singlePaired.pParams.pMinInsert
  112. --maxAlignAttempt=$singlePaired.pParams.pMaxAlignAttempt
  113. --forwardAlign=$singlePaired.pParams.pForwardAlign
  114. --reverseAlign=$singlePaired.pParams.pReverseAlign
  115. --tryHard=$singlePaired.pParams.pTryHard
  116. --valAlign=$singlePaired.pParams.pValAlign
  117. --allValAligns=$singlePaired.pParams.pAllValAligns
  118. --suppressAlign=$singlePaired.pParams.pSuppressAlign
  119. --best=$singlePaired.pParams.pBestOption.pBest
  120. #if $singlePaired.pParams.pBestOption.pBest == "doBest":
  121. --maxBacktracks=$singlePaired.pParams.pBestOption.pdMaxBacktracks
  122. --strata=$singlePaired.pParams.pBestOption.pdStrata
  123. #else:
  124. --maxBacktracks=$singlePaired.pParams.pBestOption.pnMaxBacktracks
  125. #end if
  126. --offrate=$singlePaired.pParams.pOffrate
  127. --seed=$singlePaired.pParams.pSeed
  128. #end if
  129. #end if
  130. </command>
  131. <inputs>
  132. <conditional name="refGenomeSource">
  133. <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options">
  134. <option value="indexed">Use a built-in index</option>
  135. <option value="history">Use one from the history</option>
  136. </param>
  137. <when value="indexed">
  138. <param name="index" type="select" label="Select a reference genome" help="if your genome of interest is not listed - contact Galaxy team">
  139. <options from_data_table="bowtie_indexes">
  140. <filter type="sort_by" column="2" />
  141. <validator type="no_options" message="No indexes are available" />
  142. </options>
  143. </param>
  144. </when>
  145. <when value="history">
  146. <param name="ownFile" type="data" format="bowtie_base_index,fasta" metadata_name="dbkey" label="Select the reference genome" />
  147. <conditional name="indexParams">
  148. <param name="indexSettings" type="select" label="Choose whether to use Default options for building indices or to Set your own" help="These settings are ignored when using a prebuilt index">
  149. <option value="indexPreSet">Default</option>
  150. <option value="indexFull">Set your own</option>
  151. </param>
  152. <when value="indexPreSet" />
  153. <when value="indexFull">
  154. <conditional name="autoBehavior">
  155. <param name="autoB" type="select" label="Choose to use automatic or specified behavior for some parameters (-a)" help="Allows you to set --packed, --bmax, --bmaxdivn, and --dcv">
  156. <option value="auto">Automatic behavior</option>
  157. <option value="set">Set values (sets --noauto and allows others to be set)</option>
  158. </param>
  159. <when value="auto" />
  160. <when value="set">
  161. <param name="packed" type="select" label="Whether or not to use a packed representation for DNA strings (--packed)">
  162. <option value="unpacked">Use regular representation</option>
  163. <option value="packed">Use packed representation</option>
  164. </param>
  165. <param name="bmax" type="integer" value="-1" label="Maximum number of suffixes allowed in a block (--bmax)" help="-1 for not specified. Must be at least 1" />
  166. <param name="bmaxdivn" type="integer" value="4" label="Maximum number of suffixes allowed in a block as a fraction of the length of the reference (--bmaxdivn)" />
  167. <param name="dcv" type="integer" value="1024" label="The period for the difference-cover sample (--dcv)" />
  168. </when>
  169. </conditional>
  170. <param name="nodc" type="select" label="Whether or not to disable the use of the difference-cover sample (--nodc)" help="Suffix sorting becomes quadratic-time in the worst case (with a very repetitive reference)">
  171. <option value="dc">Use difference-cover sample</option>
  172. <option value="nodc">Disable difference-cover sample</option>
  173. </param>
  174. <param name="noref" type="select" label="Whether or not to build the part of the reference index used only in paired-end alignment (-r)">
  175. <option value="ref">Build all index files</option>
  176. <option value="noref">Do not build paired-end alignment index files</option>
  177. </param>
  178. <param name="offrate" type="integer" value="5" label="How many rows get marked during annotation of some or all of the Burrows-Wheeler rows (-o)" />
  179. <param name="ftab" type="integer" value="10" label="The size of the lookup table used to calculate an initial Burrows-Wheeler range with respect to the first n characters of the query (-t)" help="ftab is 4^(n+1) bytes" />
  180. <param name="ntoa" type="select" label="Whether or not to convert Ns in the reference sequence to As (--ntoa)">
  181. <option value="no">Do not convert Ns</option>
  182. <option value="yes">Convert Ns to As</option>
  183. </param>
  184. <param name="endian" type="select" label="Endianness to use when serializing integers to the index file (--big/--little)" help="Little is most appropriate for Intel- and AMD-based architecture">
  185. <option value="little">Little</option>
  186. <option value="big">Big</option>
  187. </param>
  188. <param name="seed" type="integer" value="-1" label="Seed for the pseudorandom number generator (--seed)" help="Use -1 to use default" />
  189. <param name="cutoff" type="integer" value="-1" label="Number of first bases of the reference sequence to index (--cutoff)" help="Use -1 to use default" />
  190. </when> <!-- indexFull -->
  191. </conditional> <!-- indexParams -->
  192. </when> <!-- history -->
  193. </conditional> <!-- refGenomeSource -->
  194. <conditional name="singlePaired">
  195. <param name="sPaired" type="select" label="Is this library mate-paired?">
  196. <option value="single">Single-end</option>
  197. <option value="paired">Paired-end</option>
  198. </param>
  199. <when value="single">
  200. <param name="sInput1" type="data" format="fastqsanger,fastqillumina,fastqsolexa" label="FASTQ file" help="Must have ASCII encoded quality scores"/>
  201. <conditional name="sParams">
  202. <param name="sSettingsType" type="select" label="Bowtie settings to use" help="For most mapping needs use Commonly used settings. If you want full control use Full parameter list">
  203. <option value="preSet">Commonly used</option>
  204. <option value="full">Full parameter list</option>
  205. </param>
  206. <when value="preSet" />
  207. <when value="full">
  208. <param name="sSkip" type="integer" value="0" label="Skip the first n reads (-s)" />
  209. <param name="sAlignLimit" type="integer" value="-1" label="Only align the first n reads (-u)" help="-1 for off" />
  210. <param name="sTrimH" type="integer" value="0" label="Trim n bases from high-quality (left) end of each read before alignment (-5)" />
  211. <param name="sTrimL" type="integer" value="0" label="Trim n bases from low-quality (right) end of each read before alignment (-3)" />
  212. <param name="sMismatchSeed" type="integer" value="2" label="Maximum number of mismatches permitted in the seed (-n)" help="May be 0, 1, 2, or 3" />
  213. <param name="sMismatchQual" type="integer" value="70" label="Maximum permitted total of quality values at mismatched read positions (-e)" />
  214. <param name="sSeedLen" type="integer" value="28" label="Seed length (-l)" help="Minimum value is 5" />
  215. <param name="sRounding" type="select" label="Whether or not to round to the nearest 10 and saturating at 30 (--nomaqround)">
  216. <option value="round">Round to nearest 10</option>
  217. <option value="noRound">Do not round to nearest 10</option>
  218. </param>
  219. <param name="sMaqSoapAlign" type="integer" value="-1" label="Number of mismatches for SOAP-like alignment policy (-v)" help="-1 for default MAQ-like alignment policy" />
  220. <param name="sTryHard" type="select" label="Whether or not to try as hard as possible to find valid alignments when they exist (-y)" help="Tryhard mode is much slower than regular mode">
  221. <option value="noTryHard">Do not try hard</option>
  222. <option value="doTryHard">Try hard</option>
  223. </param>
  224. <param name="sValAlign" type="integer" value="1" label="Report up to n valid alignments per read (-k)" />
  225. <param name="sAllValAligns" type="select" label="Whether or not to report all valid alignments per read (-a)">
  226. <option value="noAllValAligns">Do not report all valid alignments</option>
  227. <option value="doAllValAligns">Report all valid alignments</option>
  228. </param>
  229. <param name="sSuppressAlign" type="integer" value="-1" label="Suppress all alignments for a read if more than n reportable alignments exist (-m)" help="-1 for no limit" />
  230. <param name="sMaxFile" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write all reads with a number of valid alignments exceeding the limit set with the -m option to a file (--max)" />
  231. <param name="sUnmappedFile" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write all reads that could not be aligned to a file (--un)" />
  232. <conditional name="sBestOption">
  233. <param name="sBest" type="select" label="Whether or not to make Bowtie guarantee that reported singleton alignments are 'best' in terms of stratum and in terms of the quality values at the mismatched positions (--best)" help="Removes all strand bias. Only affects which alignments are reported by Bowtie. Runs slower with best option">
  234. <option value="noBest">Do not use best</option>
  235. <option value="doBest">Use best</option>
  236. </param>
  237. <when value="noBest">
  238. <param name="snMaxBacktracks" type="integer" value="125" label="Maximum number of backtracks permitted when aligning a read (--maxbts)" />
  239. </when>
  240. <when value="doBest">
  241. <param name="sdMaxBacktracks" type="integer" value="800" label="Maximum number of backtracks permitted when aligning a read (--maxbts)" />
  242. <param name="sdStrata" type="select" label="Whether or not to report only those alignments that fall in the best stratum if many valid alignments exist and are reportable (--strata)">
  243. <option value="noStrata">Do not use strata option</option>
  244. <option value="doStrata">Use strata option</option>
  245. </param>
  246. </when>
  247. </conditional> <!-- bestOption -->
  248. <param name="sOffrate" type="integer" value="-1" label="Override the offrate of the index to n (-o)" help="-1 for default" />
  249. <param name="sSeed" type="integer" value="-1" label="Seed for pseudo-random number generator (--seed)" help="-1 for default" />
  250. </when> <!-- full -->
  251. </conditional> <!-- sParams -->
  252. </when> <!-- single -->
  253. <when value="paired">
  254. <param name="pInput1" type="data" format="fastqsanger,fastqillumina,fastqsolexa" label="Forward FASTQ file" help="Must have ASCII encoded quality scores"/>
  255. <param name="pInput2" type="data" format="fastqsanger,fastqillumina,fastqsolexa" label="Reverse FASTQ file" help="File format must match the Forward FASTQ file">
  256. <options options_filter_attribute="ext" from_parameter="tool.app.datatypes_registry.datatypes_by_extension" transform_lines="obj.keys()">>
  257. <column name="name" index="0"/>
  258. <column name="value" index="0"/>
  259. <filter type="param_value" ref="pInput1" ref_attribute="ext" column="0"/>
  260. </options>
  261. </param>
  262. <param name="pMaxInsert" type="integer" value="1000" label="Maximum insert size for valid paired-end alignments (-X)" />
  263. <param name="pMateOrient" type="select" label="The upstream/downstream mate orientation for valid paired-end alignment against the forward reference strand (--fr/--rf/--ff)">
  264. <option value="fr">FR (for Illumina)</option>
  265. <option value="rf">RF</option>
  266. <option value="ff">FF (for SOLiD)</option>
  267. </param>
  268. <conditional name="pParams">
  269. <param name="pSettingsType" type="select" label="Bowtie settings to use" help="For most mapping needs use Commonly used settings. If you want full control use Full parameter list">
  270. <option value="preSet">Commonly used</option>
  271. <option value="full">Full parameter list</option>
  272. </param>
  273. <when value="preSet" />
  274. <when value="full">
  275. <param name="pSkip" type="integer" value="0" label="Skip the first n pairs (-s)" />
  276. <param name="pAlignLimit" type="integer" value="-1" label="Only align the first n pairs (-u)" help="-1 for off" />
  277. <param name="pTrimH" type="integer" value="0" label="Trim n bases from high-quality (left) end of each read before alignment (-5)" />
  278. <param name="pTrimL" type="integer" value="0" label="Trim n bases from low-quality (right) end of each read before alignment (-3)" />
  279. <param name="pMismatchSeed" type="integer" value="2" label="Maximum number of mismatches permitted in the seed (-n)" help="May be 0, 1, 2, or 3" />
  280. <param name="pMismatchQual" type="integer" value="70" label="Maximum permitted total of quality values at mismatched read positions (-e)" />
  281. <param name="pSeedLen" type="integer" value="28" label="Seed length (-l)" help="Minimum value is 5" />
  282. <param name="pRounding" type="select" label="Whether or not to round to the nearest 10 and saturating at 30 (--nomaqround)">
  283. <option value="round">Round to nearest 10</option>
  284. <option value="noRound">Do not round to nearest 10</option>
  285. </param>
  286. <param name="pMaqSoapAlign" type="integer" value="-1" label="Number of mismatches for SOAP-like alignment policy (-v)" help="-1 for default MAQ-like alignment policy" />
  287. <param name="pMinInsert" type="integer" value="0" label="Minimum insert size for valid paired-end alignments (-I)" />
  288. <param name="pMaxAlignAttempt" type="integer" value="100" label="Maximum number of attempts Bowtie will make to match an alignment for one mate with an alignment for the opposite mate (--pairtries)" />
  289. <param name="pForwardAlign" type="select" label="Choose whether or not to attempt to align the forward reference strand (--nofw)">
  290. <option value="forward">Align against the forward reference strand</option>
  291. <option value="noForward">Do not align against the forward reference strand</option>
  292. </param>
  293. <param name="pReverseAlign" type="select" label="Choose whether or not to align against the reverse-complement reference strand (--norc)">
  294. <option value="reverse">Align against the reverse-complement reference strand</option>
  295. <option value="noReverse">Do not align against the reverse-complement reference strand</option>
  296. </param>
  297. <param name="pTryHard" type="select" label="Whether or not to try as hard as possible to find valid alignments when they exist (-y)" help="Tryhard mode is much slower than regular mode">
  298. <option value="noTryHard">Do not try hard</option>
  299. <option value="doTryHard">Try hard</option>
  300. </param>
  301. <param name="pValAlign" type="integer" value="1" label="Report up to n valid arguments per pair (-k)" />
  302. <param name="pAllValAligns" type="select" label="Whether or not to report all valid alignments per pair (-a)">
  303. <option value="noAllValAligns">Do not report all valid alignments</option>
  304. <option value="doAllValAligns">Report all valid alignments</option>
  305. </param>
  306. <param name="pSuppressAlign" type="integer" value="-1" label="Suppress all alignments for a pair if more than n reportable alignments exist (-m)" help="-1 for no limit" />
  307. <param name="pMaxFile" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write all reads with a number of valid alignments exceeding the limit set with the -m option to a file (--max)" />
  308. <param name="pUnmappedFile" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write all reads that could not be aligned to a file (--un)" />
  309. <conditional name="pBestOption">
  310. <param name="pBest" type="select" label="Whether or not to make Bowtie guarantee that reported singleton alignments are 'best' in terms of stratum and in terms of the quality values at the mismatched positions (--best)" help="Removes all strand bias. Only affects which alignments are reported by Bowtie. Runs slower with best option">
  311. <option value="noBest">Do not use best</option>
  312. <option value="doBest">Use best</option>
  313. </param>
  314. <when value="noBest">
  315. <param name="pnMaxBacktracks" type="integer" value="125" label="Maximum number of backtracks permitted when aligning a read (--maxbts)" />
  316. </when>
  317. <when value="doBest">
  318. <param name="pdMaxBacktracks" type="integer" value="800" label="Maximum number of backtracks permitted when aligning a read (--maxbts)" />
  319. <param name="pdStrata" type="select" label="Whether or not to report only those alignments that fall in the best stratum if many valid alignments exist and are reportable (--strata)">
  320. <option value="noStrata">Do not use strata option</option>
  321. <option value="doStrata">Use strata option</option>
  322. </param>
  323. </when>
  324. </conditional>
  325. <param name="pOffrate" type="integer" value="-1" label="Override the offrate of the index to n (-o)" help="-1 for default" />
  326. <param name="pSeed" type="integer" value="-1" label="Seed for pseudo-random number generator (--seed)" help="-1 for default" />
  327. </when> <!-- full -->
  328. </conditional> <!-- pParams -->
  329. </when> <!-- paired -->
  330. </conditional> <!-- singlePaired -->
  331. <param name="suppressHeader" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Suppress the header in the output SAM file" help="Bowtie produces SAM with several lines of header information by default" />
  332. </inputs>
  333. <outputs>
  334. <data format="sam" name="output" label="${tool.name} on ${on_string}: mapped reads">
  335. <actions>
  336. <conditional name="refGenomeSource.genomeSource">
  337. <when value="indexed">
  338. <action type="metadata" name="dbkey">
  339. <option type="from_data_table" name="bowtie_indexes" column="1" offset="0">
  340. <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
  341. <filter type="param_value" ref="refGenomeSource.index" column="0"/>
  342. </option>
  343. </action>
  344. </when>
  345. <when value="history">
  346. <action type="metadata" name="dbkey">
  347. <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" />
  348. </action>
  349. </when>
  350. </conditional>
  351. </actions>
  352. </data>
  353. <data format="fastq" name="output_suppressed_reads_l" label="${tool.name} on ${on_string}: suppressed reads (L)">
  354. <filter>((
  355. singlePaired['sPaired'] == "single" and
  356. singlePaired['sParams']['sSettingsType'] == "full" and
  357. singlePaired['sParams']['sMaxFile'] is True
  358. ) or (
  359. singlePaired['sPaired'] == "paired" and
  360. singlePaired['pParams']['pSettingsType'] == "full" and
  361. singlePaired['pParams']['pMaxFile'] is True
  362. ))
  363. </filter>
  364. <actions>
  365. <conditional name="singlePaired.sPaired">
  366. <when value="single">
  367. <action type="format">
  368. <option type="from_param" name="singlePaired.sInput1" param_attribute="ext" />
  369. </action>
  370. </when>
  371. <when value="paired">
  372. <action type="format">
  373. <option type="from_param" name="singlePaired.pInput1" param_attribute="ext" />
  374. </action>
  375. </when>
  376. </conditional>
  377. </actions>
  378. </data>
  379. <data format="fastq" name="output_suppressed_reads_r" label="${tool.name} on ${on_string}: suppressed reads (R)">
  380. <filter>singlePaired['sPaired'] == "paired"</filter>
  381. <filter>singlePaired['pParams']['pSettingsType'] == "full"</filter>
  382. <filter>singlePaired['pParams']['pMaxFile'] is True</filter>
  383. <actions>
  384. <conditional name="singlePaired.sPaired">
  385. <when value="single">
  386. <action type="format">
  387. <option type="from_param" name="singlePaired.sInput1" param_attribute="ext" />
  388. </action>
  389. </when>
  390. <when value="paired">
  391. <action type="format">
  392. <option type="from_param" name="singlePaired.pInput1" param_attribute="ext" />
  393. </action>
  394. </when>
  395. </conditional>
  396. </actions>
  397. </data>
  398. <data format="fastq" name="output_unmapped_reads_l" label="${tool.name} on ${on_string}: unmapped reads (L)">
  399. <filter>
  400. ((
  401. singlePaired['sPaired'] == "single" and
  402. singlePaired['sParams']['sSettingsType'] == "full" and
  403. singlePaired['sParams']['sUnmappedFile'] is True
  404. ) or (
  405. singlePaired['sPaired'] == "paired" and
  406. singlePaired['pParams']['pSettingsType'] == "full" and
  407. singlePaired['pParams']['pUnmappedFile'] is True
  408. ))
  409. </filter>
  410. <actions>
  411. <conditional name="singlePaired.sPaired">
  412. <when value="single">
  413. <action type="format">
  414. <option type="from_param" name="singlePaired.sInput1" param_attribute="ext" />
  415. </action>
  416. </when>
  417. <when value="paired">
  418. <action type="format">
  419. <option type="from_param" name="singlePaired.pInput1" param_attribute="ext" />
  420. </action>
  421. </when>
  422. </conditional>
  423. </actions>
  424. </data>
  425. <data format="fastq" name="output_unmapped_reads_r" label="${tool.name} on ${on_string}: unmapped reads (R)">
  426. <filter>singlePaired['sPaired'] == "paired"</filter>
  427. <filter>singlePaired['pParams']['pSettingsType'] == "full"</filter>
  428. <filter>singlePaired['pParams']['pUnmappedFile'] is True</filter>
  429. <actions>
  430. <conditional name="singlePaired.sPaired">
  431. <when value="single">
  432. <action type="format">
  433. <option type="from_param" name="singlePaired.sInput1" param_attribute="ext" />
  434. </action>
  435. </when>
  436. <when value="paired">
  437. <action type="format">
  438. <option type="from_param" name="singlePaired.pInput1" param_attribute="ext" />
  439. </action>
  440. </when>
  441. </conditional>
  442. </actions>
  443. </data>
  444. </outputs>
  445. <tests>
  446. <test>
  447. <!--
  448. Bowtie command:
  449. bowtie -q -p 4 -S +sam-nohead chrM_base test-data/bowtie_in2.fastqsanger > bowtie_out6_u.sam
  450. sort bowtie_out6_u.sam > bowtie_out6.sam
  451. -p is the number of threads, which is hardcoded above. You need to replace the + with 2 dashes.
  452. chrM_base needs to be the base location/name of the index files.
  453. -->
  454. <param name="genomeSource" value="indexed" />
  455. <!-- this is the backwards-compatible "unique value" for this index, not an actual path -->
  456. <param name="index" value="equCab2chrM" />
  457. <param name="sPaired" value="single" />
  458. <param name="sInput1" ftype="fastqsanger" value="bowtie_in2.fastqsanger" />
  459. <param name="sSettingsType" value="preSet" />
  460. <param name="suppressHeader" value="true" />
  461. <output name="output" ftype="sam" file="bowtie_out6.sam" sort="True" />
  462. </test>
  463. <test>
  464. <!--
  465. Bowtie command:
  466. bowtie-build -f test-data/phiX.fasta phiX_base
  467. bowtie -q -X 1000 +ff -p 4 -S +sam-nohead -n 2 -e 70 -l 28 +pairtries 100 +maxbts 800 +best +un bowtie_out8_u.fastq phiX_base -1 test-data/bowtie_in5.fastqsanger -2 test-data/bowtie_in6.fastqsanger > bowtie_out7_u.sam
  468. sort bowtie_out7_u.sam > bowtie_out7.sam
  469. sort bowtie_out8_u_1.sam > bowtie_out8_1.sam
  470. sort bowtie_out8_u_2.sam > bowtie_out8_2.sam
  471. Then also need to modify bowtie_out8_1.sam and bowtie_out8_2.sam so that all @ lines come before sequence lines.
  472. -p is the number of threads, hardcoded above. You need to replace the + with 2 dashes.
  473. The two unmapped output files will be named bowtie_out8_1.fastq and bowtie_out8_2.fastq.
  474. chrM_base is the index files' location/base name.
  475. -->
  476. <param name="genomeSource" value="history" />
  477. <param name="ownFile" value="phiX.fasta" />
  478. <param name="indexSettings" value="indexPreSet" />
  479. <param name="sPaired" value="paired" />
  480. <param name="pInput1" ftype="fastqsanger" value="bowtie_in5.fastqsanger" />
  481. <param name="pInput2" ftype="fastqsanger" value="bowtie_in6.fastqsanger" />
  482. <param name="pMaxInsert" value="1000" />
  483. <param name="pMateOrient" value="ff" />
  484. <param name="pSettingsType" value="full" />
  485. <param name="pSkip" value="0" />
  486. <param name="pAlignLimit" value="-1" />
  487. <param name="pTrimH" value="0" />
  488. <param name="pTrimL" value="0" />
  489. <param name="pMismatchSeed" value="2" />
  490. <param name="pMismatchQual" value="70" />
  491. <param name="pSeedLen" value="28" />
  492. <param name="pRounding" value="round" />
  493. <param name="pMaqSoapAlign" value="-1" />
  494. <param name="pMinInsert" value="0" />
  495. <param name="pMaxAlignAttempt" value="100" />
  496. <param name="pForwardAlign" value="forward" />
  497. <param name="pReverseAlign" value="reverse" />
  498. <param name="pTryHard" value="noTryHard" />
  499. <param name="pValAlign" value="1" />
  500. <param name="pAllValAligns" value="noAllValAligns" />
  501. <param name="pSuppressAlign" value="-1" />
  502. <param name="pUnmappedFile" value="true" />
  503. <param name="pMaxFile" value="false" />
  504. <param name="pBest" value="doBest" />
  505. <param name="pdMaxBacktracks" value="800" />
  506. <param name="pdStrata" value="noStrata" />
  507. <param name="pOffrate" value="-1" />
  508. <param name="pSeed" value="-1" />
  509. <param name="suppressHeader" value="true" />
  510. <output name="output" ftype="sam" file="bowtie_out7.sam" sort="True" />
  511. <output name="output_unmapped_reads_l" ftype="fastqsanger" file="bowtie_out8_1.fastq" sort="True" />
  512. <output name="output_unmapped_reads_r" ftype="fastqsanger" file="bowtie_out8_2.fastq" sort="True" />
  513. </test>
  514. <!-- start testing of non-sanger variant fastq reads -->
  515. <test>
  516. <param name="genomeSource" value="history" />
  517. <param name="ownFile" value="phiX.fasta" />
  518. <param name="indexSettings" value="indexPreSet" />
  519. <param name="sPaired" value="paired" />
  520. <param name="pInput1" ftype="fastqillumina" value="bowtie_in5.fastqillumina" />
  521. <param name="pInput2" ftype="fastqillumina" value="bowtie_in6.fastqillumina" />
  522. <param name="pMaxInsert" value="1000" />
  523. <param name="pMateOrient" value="ff" />
  524. <param name="pSettingsType" value="full" />
  525. <param name="pSkip" value="0" />
  526. <param name="pAlignLimit" value="-1" />
  527. <param name="pTrimH" value="0" />
  528. <param name="pTrimL" value="0" />
  529. <param name="pMismatchSeed" value="2" />
  530. <param name="pMismatchQual" value="70" />
  531. <param name="pSeedLen" value="28" />
  532. <param name="pRounding" value="round" />
  533. <param name="pMaqSoapAlign" value="-1" />
  534. <param name="pMinInsert" value="0" />
  535. <param name="pMaxAlignAttempt" value="100" />
  536. <param name="pForwardAlign" value="forward" />
  537. <param name="pReverseAlign" value="reverse" />
  538. <param name="pTryHard" value="noTryHard" />
  539. <param name="pValAlign" value="1" />
  540. <param name="pAllValAligns" value="noAllValAligns" />
  541. <param name="pSuppressAlign" value="-1" />
  542. <param name="pUnmappedFile" value="true" />
  543. <param name="pMaxFile" value="false" />
  544. <param name="pBest" value="doBest" />
  545. <param name="pdMaxBacktracks" value="800" />
  546. <param name="pdStrata" value="noStrata" />
  547. <param name="pOffrate" value="-1" />
  548. <param name="pSeed" value="-1" />
  549. <param name="suppressHeader" value="true" />
  550. <output name="output" ftype="sam" file="bowtie_out7.sam" sort="True" />
  551. <output name="output_unmapped_reads_l" ftype="fastqillumna" file="bowtie_out8_1.fastqillumina.sorted" sort="True" />
  552. <output name="output_unmapped_reads_r" ftype="fastqillumna" file="bowtie_out8_2.fastqillumina.sorted" sort="True" />
  553. </test>
  554. <test>
  555. <param name="genomeSource" value="history" />
  556. <param name="ownFile" value="phiX.fasta" />
  557. <param name="indexSettings" value="indexPreSet" />
  558. <param name="sPaired" value="paired" />
  559. <param name="pInput1" ftype="fastqsolexa" value="bowtie_in5.fastqsolexa" />
  560. <param name="pInput2" ftype="fastqsolexa" value="bowtie_in6.fastqsolexa" />
  561. <param name="pMaxInsert" value="1000" />
  562. <param name="pMateOrient" value="ff" />
  563. <param name="pSettingsType" value="full" />
  564. <param name="pSkip" value="0" />
  565. <param name="pAlignLimit" value="-1" />
  566. <param name="pTrimH" value="0" />
  567. <param name="pTrimL" value="0" />
  568. <param name="pMismatchSeed" value="2" />
  569. <param name="pMismatchQual" value="70" />
  570. <param name="pSeedLen" value="28" />
  571. <param name="pRounding" value="round" />
  572. <param name="pMaqSoapAlign" value="-1" />
  573. <param name="pMinInsert" value="0" />
  574. <param name="pMaxAlignAttempt" value="100" />
  575. <param name="pForwardAlign" value="forward" />
  576. <param name="pReverseAlign" value="reverse" />
  577. <param name="pTryHard" value="noTryHard" />
  578. <param name="pValAlign" value="1" />
  579. <param name="pAllValAligns" value="noAllValAligns" />
  580. <param name="pSuppressAlign" value="-1" />
  581. <param name="pUnmappedFile" value="true" />
  582. <param name="pMaxFile" value="false" />
  583. <param name="pBest" value="doBest" />
  584. <param name="pdMaxBacktracks" value="800" />
  585. <param name="pdStrata" value="noStrata" />
  586. <param name="pOffrate" value="-1" />
  587. <param name="pSeed" value="-1" />
  588. <param name="suppressHeader" value="true" />
  589. <output name="output" ftype="sam" file="bowtie_out7.sam" sort="True" />
  590. <output name="output_unmapped_reads_l" ftype="fastqsolexa" file="bowtie_out8_1.fastqsolexa.sorted" sort="True" />
  591. <output name="output_unmapped_reads_r" ftype="fastqsolexa" file="bowtie_out8_2.fastqsolexa.sorted" sort="True" />
  592. </test>
  593. <!-- end testing of non-sanger variant fastq reads -->
  594. <test>
  595. <!--
  596. Bowtie command:
  597. bowtie -q -p 4 -S +sam-nohead -n 2 -e 70 -l 28 +maxbts 125 -y -k 1 chrM_base test-data/bowtie_in2.fastqsanger > bowtie_out9_u.sam
  598. sort bowtie_out9_u.sam > bowtie_out9.sam
  599. -p is the number of threads, hardcoded above. You need to replace the + with 2 dashes.
  600. chrM_base is the index files' location/base name.
  601. -->
  602. <param name="genomeSource" value="indexed" />
  603. <!-- this is the backwards-compatible "unique value" for this index, not an actual path -->
  604. <param name="index" value="equCab2chrM" />
  605. <param name="sPaired" value="single" />
  606. <param name="sInput1" ftype="fastqsanger" value="bowtie_in2.fastqsanger" />
  607. <param name="sSettingsType" value="full" />
  608. <param name="sSkip" value="0" />
  609. <param name="sAlignLimit" value="-1" />
  610. <param name="sTrimH" value="0" />
  611. <param name="sTrimL" value="0" />
  612. <param name="sMismatchSeed" value="2" />
  613. <param name="sMismatchQual" value="70" />
  614. <param name="sSeedLen" value="28" />
  615. <param name="sRounding" value="round" />
  616. <param name="sMaqSoapAlign" value="-1" />
  617. <param name="sTryHard" value="doTryHard" />
  618. <param name="sValAlign" value="1" />
  619. <param name="sAllValAligns" value="noAllValAligns" />
  620. <param name="sSuppressAlign" value="-1" />
  621. <param name="sUnmappedFile" value="false" />
  622. <param name="sMaxFile" value="false" />
  623. <param name="sBest" value="noBest" />
  624. <param name="snMaxBacktracks" value="125" />
  625. <param name="sOffrate" value="-1" />
  626. <param name="sSeed" value="-1" />
  627. <param name="suppressHeader" value="true" />
  628. <output name="output" ftype="sam" file="bowtie_out9.sam" sort="True" />
  629. </test>
  630. <test>
  631. <!--
  632. Bowtie command:
  633. bowtie-build +offrate 5 +ftabchars 10 +little -f test-data/phiX.fasta phiX_base
  634. bowtie -q -X 1000 +ff -p 4 -S +sam-nohead phiX_base -1 test-data/bowtie_in5.fastqsanger -2 test-data/bowtie_in6.fastqsanger > bowtie_out10_u.sam
  635. sort bowtie_out10_u.sam > bowtie_out10.sam
  636. -p is the number of threads, hardcoded above. You need to replace the + with 2 dashes.
  637. chrM_base is the index files' location/base name.
  638. -->
  639. <param name="genomeSource" value="history" />
  640. <param name="ownFile" value="phiX.fasta" />
  641. <param name="indexSettings" value="indexFull" />
  642. <param name="autoB" value="auto" />
  643. <param name="nodc" value="dc" />
  644. <param name="noref" value="ref" />
  645. <param name="offrate" value="5" />
  646. <param name="ftab" value="10" />
  647. <param name="ntoa" value="no" />
  648. <param name="endian" value="little" />
  649. <param name="seed" value="-1" />
  650. <param name="cutoff" value="-1" />
  651. <param name="sPaired" value="paired" />
  652. <param name="pInput1" ftype="fastqsanger" value="bowtie_in5.fastqsanger" />
  653. <param name="pInput2" ftype="fastqsanger" value="bowtie_in6.fastqsanger" />
  654. <param name="pMaxInsert" value="1000" />
  655. <param name="pMateOrient" value="ff" />
  656. <param name="pSettingsType" value="preSet" />
  657. <param name="suppressHeader" value="true" />
  658. <output name="output" ftype="sam" file="bowtie_out10.sam" sort="True" />
  659. </test>
  660. </tests>
  661. <help>
  662. **What it does**
  663. Bowtie_ is a short read aligner designed to be ultrafast and memory-efficient. It is developed by Ben Langmead and Cole Trapnell. Please cite: Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biology 10:R25.
  664. .. _Bowtie: http://bowtie-bio.sourceforge.net/index.shtml
  665. ------
  666. **Know what you are doing**
  667. .. class:: warningmark
  668. There is no such thing (yet) as an automated gearshift in short read mapping. It is all like stick-shift driving in San Francisco. In other words = running this tool with default parameters will probably not give you meaningful results. A way to deal with this is to **understand** the parameters by carefully reading the `documentation`__ and experimenting. Fortunately, Galaxy makes experimenting easy.
  669. .. __: http://bowtie-bio.sourceforge.net/index.shtml
  670. ------
  671. **Input formats**
  672. Bowtie accepts files in Sanger FASTQ format. Use the FASTQ Groomer to prepare your files.
  673. ------
  674. **A Note on Built-in Reference Genomes**
  675. Some genomes have multiple variants. If only one "type" of genome is listed, it is the Full version, which means that everything that came in the original genome data download (possibly with mitochondrial and plasmid DNA added if it wasn't already included). The Full version is available for every genome. Some genomes also come in the Canonical variant, which contains only the "canonical" (well-defined) chromosomes or segments, such as chr1-chr22, chrX, chrY, and chrM for human. Other variations include gender. These will come in the canonical form only, so the general Canonical variant is actually Canonical Female and the other is Canonical Male (identical to female excluding chrX).
  676. ------
  677. **Outputs**
  678. The output is in SAM format, and has the following columns::
  679. Column Description
  680. -------- --------------------------------------------------------
  681. 1 QNAME Query (pair) NAME
  682. 2 FLAG bitwise FLAG
  683. 3 RNAME Reference sequence NAME
  684. 4 POS 1-based leftmost POSition/coordinate of clipped sequence
  685. 5 MAPQ MAPping Quality (Phred-scaled)
  686. 6 CIGAR extended CIGAR string
  687. 7 MRNM Mate Reference sequence NaMe ('=' if same as RNAME)
  688. 8 MPOS 1-based Mate POSition
  689. 9 ISIZE Inferred insert SIZE
  690. 10 SEQ query SEQuence on the same strand as the reference
  691. 11 QUAL query QUALity (ASCII-33 gives the Phred base quality)
  692. 12 OPT variable OPTional fields in the format TAG:VTYPE:VALUE
  693. The flags are as follows::
  694. Flag Description
  695. ------ -------------------------------------
  696. 0x0001 the read is paired in sequencing
  697. 0x0002 the read is mapped in a proper pair
  698. 0x0004 the query sequence itself is unmapped
  699. 0x0008 the mate is unmapped
  700. 0x0010 strand of the query (1 for reverse)
  701. 0x0020 strand of the mate
  702. 0x0040 the read is the first read in a pair
  703. 0x0080 the read is the second read in a pair
  704. 0x0100 the alignment is not primary
  705. It looks like this (scroll sideways to see the entire example)::
  706. QNAME FLAG RNAME POS MAPQ CIAGR MRNM MPOS ISIZE SEQ QUAL OPT
  707. HWI-EAS91_1_30788AAXX:1:1:1761:343 4 * 0 0 * * 0 0 AAAAAAANNAAAAAAAAAAAAAAAAAAAAAAAAAAACNNANNGAGTNGNNNNNNNGCTTCCCACAGNNCTGG hhhhhhh;;hhhhhhhhhhh^hOhhhhghhhfhhhgh;;h;;hhhh;h;;;;;;;hhhhhhghhhh;;Phhh
  708. HWI-EAS91_1_30788AAXX:1:1:1578:331 4 * 0 0 * * 0 0 GTATAGANNAATAAGAAAAAAAAAAATGAAGACTTTCNNANNTCTGNANNNNNNNTCTTTTTTCAGNNGTAG hhhhhhh;;hhhhhhhhhhhhhhhhhhhhhhhhhhhh;;h;;hhhh;h;;;;;;;hhhhhhhhhhh;;hhVh
  709. -------
  710. **Bowtie settings**
  711. All of the options have a default value. You can change any of them. Most of the options in Bowtie have been implemented here.
  712. ------
  713. **Bowtie parameter list**
  714. This is an exhaustive list of Bowtie options:
  715. For indexing (bowtie-build)::
  716. -a No auto behavior. Disable the default behavior where bowtie automatically
  717. selects values for --bmax/--bmaxdivn/--dcv/--packed parameters according
  718. to the memory available. [off]
  719. --packed Packing. Use a packed representation for DNA strings. [auto]
  720. --bmax INT Suffix maximum. The maximum number of suffixes allowed in a block. [auto]
  721. --bmaxdivn INT Suffix maximum fraction. The maximum number of suffixes allowed in a block
  722. expressed as a fraction of the length of the reference. [4]
  723. --dcv INT Difference-cover sample. Use INT as the period for the difference-cover
  724. sample. [1024]
  725. --nodc INT No difference-cover sample. Disable the difference-cover sample. [off]
  726. -r No reference indexes. Do not build the NAME.3.ebwt and NAME.4.ebwt portions
  727. of the index. Used only for paired-end alignment. [off]
  728. -o Offrate. How many Burrows-Wheeler rows get marked by the indexer. The
  729. indexer will mark every 2^INT rows. The marked rows correspond to rows on
  730. the genome. [5]
  731. -t INT Ftab. The lookup table used to calculate an initial Burrows-Wheeler range
  732. with respect to the first INT characters of the query. Ftab is 4^INT+1
  733. bytes. [10]
  734. --ntoa N conversion. Convert Ns to As before building the index. Otherwise, Ns are
  735. simply excluded from the index and Bowtie will not find alignments that
  736. overlap them. [off]
  737. --big Endianness. Endianness to use when serializing integers to the index file. [off]
  738. --little Endianness. [--little]
  739. --seed INT Random seed. Use INT as the seed for the pseudo-random number generator. [off]
  740. --cutoff INT Cutoff. Index only the first INT bases of the reference sequences (cumulative
  741. across sequences) and ignore the rest. [off]
  742. For aligning (bowtie)::
  743. -s INT Skip. Do not align the first INT reads or pairs in the input. [off]
  744. -u INT Align limit. Only align the first INT reads/pairs from the input. [no limit]
  745. -5 INT High-quality trim. Trim INT bases from the high-quality (left) end of each
  746. read before alignment. [0]
  747. -3 INT Low-quality trim. Trim INT bases from the low-quality (right) end of each
  748. read before alignment. [0]
  749. -n INT Mismatch seed. Maximum number of mismatches permitted in the seed (defined
  750. with seed length option). Can be 0, 1, 2, or 3. [2]
  751. -e INT Mismatch quality. Maximum permitted total of quality values at mismatched
  752. read positions. Bowtie rounds quality values to the nearest 10 and saturates
  753. at 30. [70]
  754. -l INT Seed length. The number of bases on the high-quality end of the read to
  755. which the -n ceiling applies. Must be at least 5. [28]
  756. --nomaqround Suppress MAQ rounding. Values are internally rounded to the nearest 10 and
  757. saturate at 30. This options turns off that rounding. [off]
  758. -v INT MAQ- or SOAP-like alignment policy. This option turns off the default
  759. MAQ-like alignment policy in favor of a SOAP-like one. End-to-end alignments
  760. with at most INT mismatches. [off]
  761. -I INT Minimum insert. The minimum insert size for valid paired-end alignments.
  762. Does checking on untrimmed reads if -5 or -3 is used. [0]
  763. -X INT Maximum insert. The maximum insert size for valid paired-end alignments.
  764. Does checking on untrimmed reads if -5 or -3 is used. [250]
  765. --fr Mate orientation. The upstream/downstream mate orientations for a valid
  766. paired-end alignment against the forward reference strand. [--fr]
  767. --rf Mate orientation. [off]
  768. --ff Mate orientation. [off]
  769. --pairtries INT Maximum alignment attempts for paired-end data. [100]
  770. --nofw No forward aligning. Choosing this option means that Bowtie will not attempt
  771. to align against the forward reference strand. [off]
  772. --norc No reverse-complement aligning. Setting this will mean that Bowtie will not
  773. attempt to align against the reverse-complement reference strand. [off]
  774. --un FILENAME Write all reads that could not be aligned to file [off]
  775. --max FILENAME Write all reads with a number of valid alignments exceeding the limit
  776. set with the -m option to file [off]
  777. --maxbts INT Maximum backtracks. The maximum number of backtracks permitted when aligning
  778. a read in -n 2 or -n 3 mode. [125 without --best] [800 with --best]
  779. -y Try hard. Try as hard as possible to find valid alignments when they exist,
  780. including paired-end alignments. [off]
  781. --chunkmbs INT Thread memory. The number of megabytes of memory a given thread is given to
  782. store path descriptors in --best mode. [32]
  783. -k INT Valid alignments. The number of valid alignments per read or pair. [off]
  784. -a All valid alignments. Choosing this means that all valid alignments per read
  785. or pair will be reported. [off]
  786. -m INT Suppress alignments. Suppress all alignments for a particular read or pair
  787. if more than INT reportable alignments exist for it. [no limit]
  788. --best Best mode. Make Bowtie guarantee that reported singleton alignments are
  789. "best" in terms of stratum (the number of mismatches) and quality values at
  790. mismatched position. [off]
  791. --strata Best strata. When running in best mode, report alignments that fall into the
  792. best stratum if there are ones falling into more than one. [off]
  793. -o INT Offrate override. Override the offrate of the index with INT. Some row
  794. markings are discarded when index read into memory. INT must be greater than
  795. the value used to build the index (default: 5). [off]
  796. --seed INT Random seed. Use INT as the seed for the pseudo-random number generator. [off]
  797. --snpphred INT Use INT as the SNP penalty for decoding colorspace alignments. True ratio of
  798. SNPs per base in the subject genome. [see --snpfrac]
  799. --snpfrac DEC Use DEC as the estimated ratio of SNPs per base when decoding colorspace
  800. alignments. [0.001]
  801. --col-keepends Keep the extreme-end nucleotides and qualities when decoding colorspace
  802. alignments. [off]
  803. </help>
  804. </tool>