Input and Output¶
Inputs¶
fragment file or Cell Ranger matrix directory; when using a fragment file, the workflow sorts it internally by barcode and genomic position by default
reference genome FASTA
blacklist BED file
Outputs¶
outdir/outs/result_table.tsv.gzwith the consensus Holmes+Watson CNV tableoutdir/count_matrix.h5adwith the filtered count matrix used for inferenceoutdir/parameter_configuration.txtwith the run configurationoutdir/binned_genome.csvwith the genome bins and GC annotationsoutdir/breakpoints.csvwith the detected breakpoints per celloutdir/clusters.jsonwith the inferred segment clusters per celloutdir/outs/Karyogram.pngwhen plotting is enabledoutdir/outs/integer_states.tsv.gzwith integer CNV statesoutdir/outs/continuous_scores.tsv.gzwith continuous CNV scoresoutdir/outs/result_table_holmes.tsv.gzwith Holmes-mapped CNV statesoutdir/outs/result_table_watson.tsv.gzwith Watson-mapped CNV statesoutdir/outs/scaling_factors.tsv.gzwith per-cell scaling factors