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Update tool_conf.xml.* to only use the generic python FASTQ to FASTA converter by default.
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+4
-2
@@ -52,7 +52,7 @@
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<tool file="maf/maf_to_interval.xml" />
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<tool file="maf/maf_to_fasta.xml" />
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<tool file="fasta_tools/tabular_to_fasta.xml" />
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<tool file="fastx_toolkit/fastq_to_fasta.xml" />
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<tool file="fastq/fastq_to_fasta.xml" />
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</section>
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<section name="FASTA manipulation" id="fasta_manipulation">
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<tool file="fasta_tools/fasta_compute_length.xml" />
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@@ -289,7 +289,9 @@
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<tool file="fastx_toolkit/fastx_quality_statistics.xml" />
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<tool file="fastx_toolkit/fastq_quality_boxplot.xml" />
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<tool file="fastx_toolkit/fastx_nucleotides_distribution.xml" />
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<tool file="metag_tools/split_paired_reads.xml" /> -->
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<tool file="metag_tools/split_paired_reads.xml" />
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<tool file="fastx_toolkit/fastq_to_fasta.xml" />
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-->
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<label text="Roche-454 data" id="454" />
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<tool file="metag_tools/short_reads_figure_score.xml" />
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<tool file="metag_tools/short_reads_trim_seq.xml" />
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@@ -80,7 +80,7 @@
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<tool file="maf/maf_to_interval.xml" />
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<tool file="maf/maf_to_fasta.xml" />
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<tool file="fasta_tools/tabular_to_fasta.xml" />
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<tool file="fastx_toolkit/fastq_to_fasta.xml" />
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<tool file="fastq/fastq_to_fasta.xml" />
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<tool file="filters/wiggle_to_simple.xml" />
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<tool file="filters/sff_extractor.xml" />
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<tool file="filters/gtf2bedgraph.xml" />
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@@ -212,7 +212,9 @@
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<tool file="fastx_toolkit/fastx_quality_statistics.xml" />
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<tool file="fastx_toolkit/fastq_quality_boxplot.xml" />
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<tool file="fastx_toolkit/fastx_nucleotides_distribution.xml" />
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<tool file="metag_tools/split_paired_reads.xml" /> -->
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<tool file="metag_tools/split_paired_reads.xml"
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<tool file="fastx_toolkit/fastq_to_fasta.xml" />
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-->
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<label text="Roche-454 data" id="454" />
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<tool file="metag_tools/short_reads_figure_score.xml" />
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<tool file="metag_tools/short_reads_trim_seq.xml" />
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