Mercurial > repos > jjohnson > cistrome_beta
diff beta_basic.xml @ 2:9c5241259454 draft
planemo upload for repository https://github.com/jj-umn/galaxytools/tree/master/cistrome_beta commit 76ad167e754d8254ee4e9c6d2047c84c5f2da55a-dirty
| author | jjohnson |
|---|---|
| date | Thu, 22 Mar 2018 08:33:55 -0400 |
| parents | 20453b656907 |
| children | 067573bac905 |
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--- a/beta_basic.xml Tue Sep 16 12:51:50 2014 -0500 +++ b/beta_basic.xml Thu Mar 22 08:33:55 2018 -0400 @@ -1,61 +1,61 @@ <tool id="beta_basic" name="BETA-basic: Binding and Expression Target Analysis" version="0.1.0"> - <description>Predict the factors (TFs or CRs) direct target genes by combining the binding and expression data</description> - <macros> - <import>beta_macros.xml</import> - </macros> - <expand macro="requirements" /> - <command> - BETA basic - #include source=$common_opts# - #include source=$genome_opts# - #include source=$extended_opts# - &> $log - </command> - <inputs> - <expand macro="common_params" /> - <expand macro="genome_params" /> - <expand macro="extended_params" /> - </inputs> - <expand macro="stdio" /> - <outputs> - <data format="txt" name="log" label="Log of BETA basic"/> - <data format="pdf" name="functionoutput" label="BETA functional prediction on ${peakfile.name}" from_work_dir="BETA_OUTPUT/NA_function_prediction.pdf"/> - <data format="tabular" name="uptargetsoutput" label="BETA direct targets prediction on up regulated genes" from_work_dir="BETA_OUTPUT/NA_uptarget.txt"/> - <data format="tabular" name="downtargetsoutput" label="BETA direct targets prediction on down regulated genes" from_work_dir="BETA_OUTPUT/NA_downtarget.txt"/> - <data format="bed" name="uptargetpeaks" label="BETA Uptarget associated peaks" from_work_dir="BETA_OUTPUT/NA_uptarget_associate_peaks.bed"/> - <data format="bed" name="downtargetpeaks" label="BETA Downtarget associated peaks" from_work_dir="BETA_OUTPUT/NA_downtarget_associate_peaks.bed"/> - </outputs> - <tests> - <test> - <param name='peakfile' value="peaks.bed" ftype="bed" dbkey="hg19"/> - <param name="distance" value="100000"/> - <param name="peaknumber" value="10000"/> - <param name="genomeName" value="hg19"/> - <param name='exprefile' value="diff_expr.xls" ftype="tabular" dbkey="hg19"/> - <param name="kind" value="LIM"/> - <param name="expreinfo" type="text" value="2,5,7"/> - <param name="gname2" value="Refseq"/> - <param name="diff_fdr" value="1.0"/> - <param name="diff_amount" value="0.5"/> - <param name="method" value="score"/> - <output name="log"> - <assert_contents> - <has_text_matching expression="Finished" /> - </assert_contents> - </output> - <output name="targetsoutput"> - <assert_contents> - <has_text_matching expression="chr19\t4675243\t4723855\tNM_139159\t1.1.*\t-\tDPP" /> - </assert_contents> - </output> - <output name="targetpeaks"> - <assert_contents> - <has_text_matching expression="chr19\t4723422\t4724314\tregion_9\tNM_139159\tDPP9\t13\t0.6.*" /> - </assert_contents> - </output> - </test> - </tests> - <help> + <description>Predict the factors (TFs or CRs) direct target genes by combining the binding and expression data</description> + <macros> + <import>beta_macros.xml</import> + </macros> + <expand macro="requirements" /> + <expand macro="stdio" /> + <command><![CDATA[ + BETA basic + #include source=$common_opts# + #include source=$genome_opts# + #include source=$extended_opts# + &> $log + ]]></command> + <inputs> + <expand macro="common_params" /> + <expand macro="genome_params" /> + <expand macro="extended_params" /> + </inputs> + <outputs> + <data format="txt" name="log" label="Log of BETA basic"/> + <data format="pdf" name="functionoutput" label="BETA functional prediction on ${peakfile.name}" from_work_dir="BETA_OUTPUT/NA_function_prediction.pdf"/> + <data format="tabular" name="uptargetsoutput" label="BETA direct targets prediction on up regulated genes" from_work_dir="BETA_OUTPUT/NA_uptarget.txt"/> + <data format="tabular" name="downtargetsoutput" label="BETA direct targets prediction on down regulated genes" from_work_dir="BETA_OUTPUT/NA_downtarget.txt"/> + <data format="bed" name="uptargetpeaks" label="BETA Uptarget associated peaks" from_work_dir="BETA_OUTPUT/NA_uptarget_associate_peaks.bed"/> + <data format="bed" name="downtargetpeaks" label="BETA Downtarget associated peaks" from_work_dir="BETA_OUTPUT/NA_downtarget_associate_peaks.bed"/> + </outputs> + <tests> + <test> + <param name='peakfile' value="peaks.bed" ftype="bed" dbkey="hg19"/> + <param name="distance" value="100000"/> + <param name="peaknumber" value="10000"/> + <param name="genomeName" value="hg19"/> + <param name='exprefile' value="diff_expr.xls" ftype="tabular" dbkey="hg19"/> + <param name="kind" value="LIM"/> + <param name="expreinfo" value="2,5,7"/> + <param name="gname2" value="Refseq"/> + <param name="diff_fdr" value="1.0"/> + <param name="diff_amount" value="0.5"/> + <param name="method" value="score"/> + <output name="log"> + <assert_contents> + <has_text_matching expression="Finished" /> + </assert_contents> + </output> + <output name="uptargetsoutput"> + <assert_contents> + <has_text_matching expression="chr19\t4675243\t4723855\tNM_139159\t1.1.*\t-\tDPP" /> + </assert_contents> + </output> + <output name="uptargetpeaks"> + <assert_contents> + <has_text_matching expression="chr19\t4723422\t4724314\tregion_9\tNM_139159\tDPP9\t13\t0.6.*" /> + </assert_contents> + </output> + </test> + </tests> + <help><![CDATA[ ** BETA basic ** @EXTERNAL_DOCUMENTATION@ @@ -76,36 +76,36 @@ **Parameters** - **PEAKFILE file** contains peaks for the experiment in a bed - format file. Normally, it's produced by the peak calling tool. It's - required. + format file. Normally, it's produced by the peak calling tool. It's + required. - **EXPREFILE file** contains the differentially expressed genes in a tab - delimited text file. It's required. + delimited text file. It's required. - **Kind** The kind of your expression file format, LIM for LIMMA standard - output with Microarray, CUF for Cuffdiffs standard output with RNA-seq, - BSF for BETA specific format, and O for other formats. + output with Microarray, CUF for Cuffdiffs standard output with RNA-seq, + BSF for BETA specific format, and O for other formats. - **genome** hg19 for human and mm9 for mouse. Others, don't set this parameter. - **gname2** If this switch is on, gene or transcript IDs in files given - through -e will be considered as official gene symbols, DEFAULT=FALSE + through -e will be considered as official gene symbols, DEFAULT=FALSE - **EXPREINFO** is the columns info of the geneID, up/down status and statistcal - values column of your expression data,NOTE: use a comma as an connector. - for example: 2,5,7 means geneID in the 2nd column, Tscore in 5th column - and FDR in 7 column. + values column of your expression data,NOTE: use a comma as an connector. + for example: 2,5,7 means geneID in the 2nd column, Tscore in 5th column + and FDR in 7 column. - **REFERENCE** is the refgene info file downloaded from UCSC genome browser. - It is a tab delimited text file with gene annotation with refseq and gene symbol. - Input this file only if your genome is neither hg19 nor mm9. - profiling + It is a tab delimited text file with gene annotation with refseq and gene symbol. + Input this file only if your genome is neither hg19 nor mm9. + profiling - **OUTPUT** to specify the output files directory - **bl** Whether or not to use CTCF boundary file to get the contributed peaks - **BOUNDARYFILE** is the file with reasonable boundaries if --bl is on and genome - is neither hg19 nor mm9. + is neither hg19 nor mm9. - **NAME** specify the name of the output files. - **DISTANCE** specify the distance wich peaks within it will be considered. - **DIFF_FDR** specify the differential genes by the 3rd column in file input - via -e, genes with less than this value will be considered as the differentially - changed genes. + via -e, genes with less than this value will be considered as the differentially + changed genes. - **DIFF_AMOUNT** specify the differential genes the top #(DIFF_AMOUNT) ranked by - the 3rd column in file input via -e, genes ranked in the top # will be considered - as the differentially expressed genes. + the 3rd column in file input via -e, genes ranked in the top # will be considered + as the differentially expressed genes. - **CUTOFF** specify a cutoff of ks-test in the function prediction part ----- @@ -114,75 +114,66 @@ :: - -h, --help show this help message and exit - -p PEAKFILE, --peakfile PEAKFILE - The bed format of peaks binding sites. (BETA support 3 - or 5 columns bed format, CHROM, START, END (NAME, - SCORE)) - -e EXPREFILE, --diff_expr EXPREFILE - The differential expression file get from limma for - MicroArray ddata and cuffdiff for RNAseq data - -k {LIM,CUF,BSF,O}, --kind {LIM,CUF,BSF,O} - The kind of your expression file,this is required,it - can be LIM, CUF, BSF, O. LIM for LIMMA standard - format. CUF for CUFDIFF standard format, BSF for BETA - specific format and O for other formats, if is 'O', - columns infor required via --info - -g {hg19,mm9}, --genome {hg19,mm9} - Specify your species, hg19, mm9. For other genome - assembily versions of human and mouse or other - species, ignore this parameter. - --gname2 If this switch is on, gene or transcript IDs in files - given through -e will be considered as official gene - symbols, DEFAULT=FALSE - --info EXPREINFO Specify the geneID, up/down status and statistcal - values column of your expression data,NOTE: use a - comma as an connector. for example: 2,5,7 means geneID - in the 2nd column, Tscore in 5th column and FDR in 7 - column DEFAULT:2,5,7 for LIMMA; 2,10,13 for Cuffdiff - and 1,2,3 for BETA specific format - -r REFERENCE, --reference REFERENCE - The refgene info file downloaded from UCSC genome - browser.input this file only if your genome is neither - hg19 nor mm9 - -o OUTPUT, --output OUTPUT - The directory to store all the output files, if you - don't set this, files will be output into the current - directory - --bl Whether or not use CTCF boundary to filter peaks - around a gene, DEFAULT=FALSE - --bf BOUNDARYFILE CTCF conserved peaks bed file, use this only when you - set --bl and the genome is neither hg19 nor mm9 - --pn PEAKNUMBER The number of peaks you want to consider, - DEFAULT=10000 - --method {score,distance} - Define the method to do the TF/CR function prediction, - score for regulatory potential, distance for the - distance to the proximal binding peak. DEFAULT:SCORE - -n NAME, --name NAME This argument is used to name the result file.If not - set, the peakfile name will be used instead - -d DISTANCE, --distance DISTANCE - Set a number which unit is 'base'. It will get peaks - within this distance from gene TSS. default:100000 - (100kb) - --df DIFF_FDR Input a number 0~1 as a threshold to pick out the most - significant differential expressed genes by FDR, - DEFAULT = 1, that is select all the genes - --da DIFF_AMOUNT Get the most significant differential expressed genes - by the percentage(0-1) or number(larger than 1)Input a - number between 0-1, the rank based on fdr for example, - 2000, so that the script will only consider top 2000 - genes as the differentially expressed genes. DEFAULT = - 0.5, that is select top 50 percent genes of up and - down seprately. NOTE: if you want to use diff_fdr, - please set this parameter to 1, otherwise it will get - the intersection of these two parameters - -c CUTOFF, --cutoff CUTOFF - Input a number between 0~1 as a threshold to select - the closer target gene list(up regulate or down - regulate or both) with the p value was called by one - side ks-test, DEFAULT = 0.001 + -h, --help show this help message and exit + -p PEAKFILE, --peakfile PEAKFILE The bed format of peaks binding sites. (BETA support 3 + or 5 columns bed format, CHROM, START, END (NAME, + SCORE)) + -e EXPREFILE, --diff_expr EXPREFILE The differential expression file get from limma for + MicroArray ddata and cuffdiff for RNAseq data + -k {LIM,CUF,BSF,O}, --kind {LIM,CUF,BSF,O} The kind of your expression file,this is required,it + can be LIM, CUF, BSF, O. LIM for LIMMA standard + format. CUF for CUFDIFF standard format, BSF for BETA + specific format and O for other formats, if is 'O', + columns infor required via --info + -g {hg19,mm9}, --genome {hg19,mm9} Specify your species, hg19, mm9. For other genome + assembily versions of human and mouse or other + species, ignore this parameter. + --gname2 If this switch is on, gene or transcript IDs in files + given through -e will be considered as official gene + symbols, DEFAULT=FALSE + --info EXPREINFO Specify the geneID, up/down status and statistcal + values column of your expression data,NOTE: use a + comma as an connector. for example: 2,5,7 means geneID + in the 2nd column, Tscore in 5th column and FDR in 7 + column DEFAULT:2,5,7 for LIMMA; 2,10,13 for Cuffdiff + and 1,2,3 for BETA specific format + -r REFERENCE, --reference REFERENCE The refgene info file downloaded from UCSC genome + browser.input this file only if your genome is neither + hg19 nor mm9 + -o OUTPUT, --output OUTPUT The directory to store all the output files, if you + don't set this, files will be output into the current + directory + --bl Whether or not use CTCF boundary to filter peaks + around a gene, DEFAULT=FALSE + --bf BOUNDARYFILE CTCF conserved peaks bed file, use this only when you + set --bl and the genome is neither hg19 nor mm9 + --pn PEAKNUMBER The number of peaks you want to consider, + DEFAULT=10000 + --method {score,distance} Define the method to do the TF/CR function prediction, + score for regulatory potential, distance for the + distance to the proximal binding peak. DEFAULT:SCORE + -n NAME, --name NAME This argument is used to name the result file.If not + set, the peakfile name will be used instead + -d DISTANCE, --distance DISTANCE Set a number which unit is 'base'. It will get peaks + within this distance from gene TSS. default:100000 + (100kb) + --df DIFF_FDR Input a number 0~1 as a threshold to pick out the most + significant differential expressed genes by FDR, + DEFAULT = 1, that is select all the genes + --da DIFF_AMOUNT Get the most significant differential expressed genes + by the percentage(0-1) or number(larger than 1)Input a + number between 0-1, the rank based on fdr for example, + 2000, so that the script will only consider top 2000 + genes as the differentially expressed genes. DEFAULT = + 0.5, that is select top 50 percent genes of up and + down seprately. NOTE: if you want to use diff_fdr, + please set this parameter to 1, otherwise it will get + the intersection of these two parameters + -c CUTOFF, --cutoff CUTOFF Input a number between 0~1 as a threshold to select + the closer target gene list(up regulate or down + regulate or both) with the p value was called by one + side ks-test, DEFAULT = 0.001 - </help> - + ]]></help> + <expand macro="citations" /> </tool>