Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/b1/1e54124874a394ab205f9a5ade3ce9/.command.sh Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/RunParameters.xml Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/bclconvert_samplesheet.csv Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/Data/Intensities/s.locs Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/b1/1e54124874a394ab205f9a5ade3ce9/.command.run Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/Data/Intensities/BaseCalls/L005 Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/RunInfo.xml ==> STAGING COMPLETE (7 inputs) WARNING: skipping lane 1 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 2 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 3 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 4 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 6 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 7 because RunInfo.xml file lists no tiles for it WARNING: skipping lane 8 because RunInfo.xml file lists no tiles for it Sample sheet being processed by common lib? Yes SampleSheet Settings: FastqCompressionFormat = gzip NoLaneSplitting = FALSE OverrideCycles = Y151;I8;I8;Y151 SoftwareVersion = 4.3.6 Index Read 2 (i5): The barcode and UMI outputs will be processed and output in Reverse Complement of Sample Sheet inputs. OverrideCycles bases for this read will be interpreted in reverse. shared-thread-linux-native-asio output is disabled bcl-convert Version 4.4.6 Copyright (c) 2014-2025 Illumina, Inc. Command Line: --tiles s_5 --output-directory output --bcl-input-directory rundir --sample-sheet rundir/SampleSheet.csv Conversion Begins. Input BCL Information: Read Structure: Y151;I8;I8;Y151 RunInfo.xml file lists: 8 lanes, 3136 tiles BCL file format: cbcl Positions file format: slocs Filter file format: filter Conversion Information: Tile filtering: converting 392/3136 tiles Sample Count for Lane 1: 8 Lane 1 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 2: 8 Lane 2 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 3: 8 Lane 3 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 4: 8 Lane 4 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 5: 8 Sample Count for Lane 6: 8 Lane 6 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 7: 8 Lane 7 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Sample Count for Lane 8: 8 Lane 8 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?) Expected number of sample FASTQ files to be created: 16 # CPU hw threads available: 64 Parallel Tiles: 4. Threads Per Tile: 16 SW compressors: 64 SW decompressors: 32 SW FASTQ compression level: 1 Lane 5 Post-run Information: Total clusters: 1372655984 Total Genomic Reads: 2745311968 Total Genomic Input Gigabases 414.54 Minimum reads for a sample: 100403480 Maximum reads for a sample: 159334832 Average reads per sample: 134242134.25 Undetermined reads: 1671374894 Conversion Complete.