Files

The Files page provides access to the output files for each sample analysis.

BAM Files—Aligned sequences and quality scores in the BAM (*.bam) file format.
VCF Files—Variant calls in the VCF (*.vcf.gz) file format.
Genome VCF Files—Variants, references, and no calls for all sites in the genome VCF (gVCF) file format.
Summary File—Statistics for each sample.
Picard HSmetrics Output
Summary Statistics
Report PDF
Variant Table File
BAM Files
VCF Files
Genome VCF Files
Summary File
Picard HSmetrics Output
Summary Statistics
Report PDF
Variant Table File

The following is the complete list of output files:

File name

<SampleName>.time_metrics.csv

<SampleName>.wgs_contig_mean_cov.csv

<SampleName>.wgs_hist.csv

/Additional Files/<SampleName>.wgs_overall_mean_cov.csv

<SampleName>.wgs_ploidy.csv

appVersion.log

stdout.log

<SampleName>.wgs_fine_hist.csv

<SampleName>.wgs_coverage_metrics.csv

<SampleName>.target_bed_callability.bed

<SampleName>.target_bed_contig_mean_cov.csv

<SampleName>.target_bed_coverage_metrics.csv

<SampleName>.target_bed_fine_hist.csv

<SampleName>.target_bed_overall_mean_cov.csv

/Additional Files/<SampleName>.target_bed_hist.csv

/Additional Files/<SampleName>.target_bed_ploidy.csv

<SampleName>.qc-coverage-region-1_contig_mean_cov.csv

<SampleName>.qc-coverage-region-1_coverage_metrics.csv

<SampleName>.qc-coverage-region-1_fine_hist.csv

<SampleName>.qc-coverage-region-1_hist.csv

<SampleName>.qc-coverage-region-1_overall_mean_cov.csv

<SampleName>.qc-coverage-region-1_ploidy.csv

<SampleName>.qc-coverage-region-2_contig_mean_cov.csv

<SampleName>.qc-coverage-region-2_coverage_metrics.csv

<SampleName>.qc-coverage-region-2_fine_hist.csv

<SampleName>.qc-coverage-region-2_hist.csv

<SampleName>.qc-coverage-region-2_overall_mean_cov.csv

<SampleName>.roh.bed

<SampleName>.roh_metrics.csv

(if annotation is enabled) /Additional Files/<SampleName>.annotations.json

/Additional Files/<SampleName>.coverageHistogram.txt

/Additional Files/<SampleName>.fragmentlength.csv

/Additional Files/<SampleName>.report.pdf

(if Picard is enabled) /Additional Files/<SampleName>.HsMetrics.txt

(if Picard is enabled) /Additional Files/<SampleName>.PerTargetMetrics.txt

/Additional Files/<SampleName>.summary.csv

/Additional Files/<SampleName>.varianttable.txt

If output format is set to BAM, the following Map/Align files are generated

<SampleName>.mapping_metrics.csv

<SampleName>.bam

<SampleName>.bam.bai

<SampleName>.bam.md5sum

If somatic variant calling is enabled, the following files are generated

<SampleName>.baf.bw

<SampleName>.hard-filtered.baf.bw

<SampleName>.hard-filtered.vcf.gz

<SampleName>.hard-filtered.vcf.gz.md5sum

<SampleName>.hard-filtered.vcf.gz.tbi

<SampleName>.vc_metrics.csv

<SampleName>.vcf.gz

<SampleName>.vcf.gz.md5sum

<SampleName>.vcf.gz.tbi

If germline variant calling is enabled, the following files are generated

<SampleName>.baf.bw

<SampleName>.hard-filtered.baf.bw

<SampleName>.hard-filtered.gvcf.gz

<SampleName>.hard-filtered.gvcf.gz.mdsum

<SampleName>.hard-filtered.gvcf.gz.tbi

<SampleName>.vc_metrics.csv

<SampleName>.hard-filtered.vcf.gz

<SampleName>.hard-filtered.vcf.gz.tbi

If CNV is enabled, the following files are generated

<SampleName>.combined.counts.txt

<SampleName>.cnv.gff3

<SampleName>.cnv.vcf.gz

<SampleName>.cnv.vcf.gz.md5sum

<SampleName>.cnv.vcf.gz.tbi

<SampleName>.cnv_metrics.csv

<SampleName>.target.counts

<SampleName>.target.counts.bw

<SampleName>.target.counts.gc-corrected

<SampleName>.seg

<SampleName>.seg.bw

<SampleName>.seg.called

<SampleName>.seg.called.merged

<SampleName>.tn.bw

<SampleName>.tn.tsv

<SampleName>.improper.pairs.bw

If SV (Manta) is enabled, the following files are generated

<SampleName>.sv.vcf.gz

<SampleName>.sv.vcf.gz.tbi

<SampleName>.sv_metrics.csv