Output files and formats

CTAT-mutations Output Files and Formats

The primary output files generated by the pipeline include the following:

• variants.HC_init.wAnnot.vcf : the initially predicted variants
• variants.HC_hard_cutoffs_applied.vcf : variants after applying hard cutoffs to remove likely false positives.
• cancer.vcf : the subset of variants that are considered most relevant to cancer biology
• igvjs_viewer.html : self-contained web-application for interactively navigating the cancer variants.

The variant annotations and descriptions include:

Column	Description
CHROM	Chromosome
POS	The 1-based position of the variation on the given sequence.
REF	Base(s) at position in the reference genome (hg38)
ALT	Alternate base(s)
GENE	Gene name DP - combined depth across samples
QUAL	A quality score associated with the inference of the given alleles.
MQ	RMS mapping quality
RNAEDIT	A known or predicted RNA-editing site
RPT	Repeat family from UCSC Genome Browser Repeatmasker Annotations
SPLICEADJ	Variant is within specified distance of a reference exon splice boundary
FATHMM	FATHMM (Functional Analysis through Hidden Markov Models). 'Pathogenic':Cancer or damaging 'Neutral':Passanger or Tolerated.
CHASM_PVALUE	Empirical p-value (probability that passenger variant is misclassified as a driver).
CHASM_FDR	False discovery rate expected (Benjamini-Hochberg multiple testing correction).
VEST_PVALUE	Empirical p-value (probability that benign variant is misclassified as pathogenic).
VEST_FDR	Composite false discovery rate (Benjamini-Hochberg multiple testing correction) for non-silentvariants in the gene combined with Stouffer’s Z-score method.
MuPIT	MuPIT 3D structure variant link