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Copy file name to clipboardExpand all lines: docs/workflow.md
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```
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**`variants_all_sorted.vcf.gz`** - a compressed vcf file containing all variants from all samples.
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**`variants_all_sorted.vcf.gz.tbi`** - an index file for the vcf file mentioned above.
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**`samples/`** - a directory containing each of the samples to be analyzed alongside each other.
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**`Sample_1/`** - a sample directory. This will contain input data files as well as output files from RegTools.
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**`tumor_rna_alignments.bam`** - file containing aligned RNA-seq reads for the given sample.
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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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**`variants_all_sorted.vcf.gz`** - a compressed vcf file containing all variants from all samples.\
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**`variants_all_sorted.vcf.gz.tbi`** - an index file for the vcf file mentioned above.\
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**`samples/`** - a directory containing each of the samples to be analyzed alongside each other.\
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**`Sample_1/`** - a sample directory. This will contain input data files as well as output files from RegTools.\
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**`tumor_rna_alignments.bam`** - file containing aligned RNA-seq reads for the given sample.\
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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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