comparison multiplicom_primer_trimming.xml @ 1:b2125910c8fd draft default tip

changed ref genome table name

0:fadef644b886

	<param name='inputf' type='data' format='fastq,fastqsanger' label='Forward Sequences' help='Forward Reads in fastq format' />
	<param name='inputr' type='data' format='fastq,fastqsanger' label='Reverse Sequences' help='Reverse Reads in fastq format' />
	<param name='mastr' type='data' format='bed' label='MASTR file' help='Design file of the Multiplicom MASTR assay' />
	<param name='readlength' type='integer' value='250' label='Read Length' help='Applied Readlength, per read' />
	<param name="indexes" type="select" label="Reference Genome" help="Select the correct genome build" >
		<options from_data_table="twobit" >
			<filter type="sort_by" column="2" />
			<validator type="no_options" message="No indexes are available" />
		</options>
	</param>
   </inputs>

1:b2125910c8fd

	<param name='inputf' type='data' format='fastq,fastqsanger' label='Forward Sequences' help='Forward Reads in fastq format' />
	<param name='inputr' type='data' format='fastq,fastqsanger' label='Reverse Sequences' help='Reverse Reads in fastq format' />
	<param name='mastr' type='data' format='bed' label='MASTR file' help='Design file of the Multiplicom MASTR assay' />
	<param name='readlength' type='integer' value='250' label='Read Length' help='Applied Readlength, per read' />
	<param name="indexes" type="select" label="Reference Genome" help="Select the correct genome build" >
		<options from_data_table="2bit" >
			<filter type="sort_by" column="2" />
			<validator type="no_options" message="No indexes are available" />
		</options>
	</param>
   </inputs>