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Copy file name to clipboardExpand all lines: docs/workflow.md
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**`tumor_rna_alignments.bam.bai`** - index file for the above RNA-seq alignment file.\
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**`variants.vcf.gz`** - a compressed vcf file containing all variants from a given samples.\
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**`variants.vcf.gz.tbi`** - an index file for the vcf file mentioned above.\
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**`logs/`** - directory containing log or error files for a given sample.
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**`output/`** - directory containing RegTools output files for a given sample.
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**`cse_identify_filtered_*`** - RegTools output files from the initial RegTools run for a given sample. This will contain results for this sample's variants only.
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**`cse_identify_filtered_compare_*`** - RegTools output files from the second RegTools run for a given sample. This will contain results for all samples' variants.
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**`variants*.bed`** - a bedfile containing the variants considered to be splicing relevant for a given RegTools parameter. This is used later to make `all_splicing_variants*.bed`.
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**`compare_junctions/hist/`** - directory containing output from the statistics script analyze all variants across all samples.
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**`logs/`** - directory containing log or error files for a given sample.\
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**`output/`** - directory containing RegTools output files for a given sample.\
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**`cse_identify_filtered_*`** - RegTools output files from the initial RegTools run for a given sample. This will contain results for this sample's variants only.\
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**`cse_identify_filtered_compare_*`** - RegTools output files from the second RegTools run for a given sample. This will contain results for all samples' variants.\
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**`variants*.bed`** - a bedfile containing the variants considered to be splicing relevant for a given RegTools parameter. This is used later to make `all_splicing_variants*.bed`.\
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**`compare_junctions/hist/`** - directory containing output from the statistics script analyze all variants across all samples.\
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**`junction_pvalues_*.tsv`** - a file containing the output from the statistic analysis script.
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