Example Sentieon pipelines implemented in shell script. You may modify these pipelines to work with your existing bioinformatics infrastructure.
See Sentieon's Argument Correspondence application note for information on how parameters in the Sentieon tools correspond to parameters in the GATK.
- Germline variant calling
- whole-genome sequencing - Standard germline variant calling suitable for whole-genome samples.
- whole-exome sequencing - Standard germline variant calling pipeline across target intervals.
- multiple input fastq - Standard germline variant calling pipeline, modified to support multiple pirrs of input FASTQ files.
- joint calling - Standard germline variant calling pipeline with joint genotyping of multiple samples.
- CCDG/functional equivalence pipeline - A Centers for Common Disease Genomics (CCDG) functional equivalent pipeline implemented in the Sentieon tools. See Sentieon's Functional Equivalent Pipeline application note for more information.
- RNAseq - Germline variant calling from aligned RNAseq data. See the Sentieon manual for more information on this pipeline.
- Somatic variant calling
- TNscope - Improved accuracy somatic variant calling.
- default - Standard somatic variant calling with TNscope.
- 50x to 100x - Somatic variant calling with TNscope. Recommended settings for 50x to 100x coverage.
- 300x or greater - Somatic variant calling with TNscope. Recommended settings for coverage over 300x.
- unique molecular identifier (UMI) - Somatic variant calling and filtering of UMI-tagged reads.
- TNseq - Pipelines matching best practice implementations for somatic variant calling.
- tumor-normal - Somatic variant calling with TNsnv and TNhaplotyper from paired tumor-normal samples.
- tumor-only - Somatic variant calling with TNsnv and TNhaplotyper from tumor-only samples.
- TNhaplotyper2 - Somatic variant calling with TNhaplotyper2.
- TNscope - Improved accuracy somatic variant calling.