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Fig. 1 | BMC Medical Genomics

Fig. 1

From: TMBur: a distributable tumor mutation burden approach for whole genome sequencing

Fig. 1

Schematic diagram of the Nextflow workflow for the singularity container used in the TMBur pipeline. TMBur is a portable software package that contains multiple individual components, including variant caller tools (Manta-Strelka2, Mutect2, and MSIsensor2) and resources (the human genome reference sequence [hg19] and reference annotations [SNPEff Ens75]), all used to provide consistent tumor mutation burden (TMB) counts. The workflow allows for the analysis of raw, whole-genome data from pairs of samples (tumor and normal) and can be conducted with multiple pairs simultaneously

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