tanglingfung

details:
  - files: [../input/DatasetP2_SimulatedReads_1.fastq, ../input/DatasetP2_SimulatedReads_2.fastq]
    description: 'random'
    analysis: RNA-seq
    genome_build: GRCh37
    # include a lane (run group ID) for each sample
    # lane: 1
    # to do multi-sample variant calling, assign samples the same metadata / batch
    # metadata:
    #   batch: your-arbitrary-batch-name