Downloading: s3://natera-platform-sandbox/pipeline-inputs/illumina_run_folders/data/20251117_LH00166_0206_A2327GFLT3/Data/Intensities/BaseCalls/L002
Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/52/68dd9122e18b73b16022014f7a02f6/.command.sh
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/RunParameters.xml
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/52/68dd9122e18b73b16022014f7a02f6/.command.run
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 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 5 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_2 --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
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
Lane 5 will be skipped because there are no tiles to convert (not listed in RunInfo.xml tile list?)
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 2 Post-run Information:
Total clusters: 1377963340
Total Genomic Reads: 2755926680
Total Genomic Input Gigabases 416.14
Minimum reads for a sample: 99693034
Maximum reads for a sample: 158117014
Average reads per sample: 133758912.75
Undetermined reads: 1685855378
Conversion Complete.