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Diljot edited this page Dec 14, 2020
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The single cell pipeline performs analysis of single cell sequencing data producing:
aligned bams somatic copy number changes qc metrics SNVs, breakpoints and haplotype allele counts
The above analyses are implemented as a series of subcommands. Each subcommand takes as input an inputs yaml file describing both the location of input files and the metadata for those input files. Subcommands also take as input a directory or directories in which results will be output.
Inputs are provided as an input yaml file, with formats specific to each subcommand described below. Absolute paths are expected.