Workflow Requirements

The app has the following workflow requirements:

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Supports samples with paired-end reads.

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Uses BAM output files from Whole Genome Sequencing v6 as inputs.

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Minimum normal sample data set size is 150 gigabases, which equates to:

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Reads for 2 × 100—Approximately 375 million

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Reads for 2 × 150—Approximately 250 million

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Minimum tumor sample data set size is 300 gigabases, which equates to:

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Reads for 2 × 100—Approximately 750 million

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Reads for 2 × 150—Approximately 5000 million

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Maximum combined (normal+tumor) data set size is 650 gigabases, which equates to:

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Reads for 2 × 100—Approximately 3.25 billion

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Reads for 2 × 150—Approximately 2.17 billion

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This app does not support mate pair or other non-forward and -reverse styles of paired-end sequencing.

For Research Use Only. Not for use in diagnostic procedures.