Hello All,
I am facing some some problem while trying to convert bcl to fastq by using bcl2fastq-2.17 software.Partial generation of output data is the problem. R1 and R2 reads are generated for lane 4.But for Lane1,2,3, only Read2 generated and no data for other lanes.While checking the Report folder there are status report present for each lane.It will be a great help for me if any body can help me to find out the problem. Hiseq2500 is used for generating the data.
The following command I used for bcl to fastq conversion.
nohup bcl2fastq \
--runfolder-dir /data/coredata/genomics/hiseq/150827_SN1046_0229_BC6WPEACXX/ \
--output-dir /data/coredata/genomics/hiseq/150827_SN1046_0229_BC6WPEACXX/TEST/ \
--sample-sheet /data/coredata/genomics/hiseq/150827_SN1046_0229_BC6WPEACXX/SampleSheet.csv \
--use-bases-mask Y*,I8n*,Y* \
--barcode-mismatches 2 -l DEBUG &
Sample sheet Format is below:
[Data],,,,,,,,
Lane,Sample_ID,Sample_Name,Sample_Plate,Sample_Well,Index_ID,Index,Sample_Project,Description
1,DPWGS-00088,DPWGS-00088,,,,NoIndex,DatePalm_-_Date_Fruits,
2,DPWGS-00089,DPWGS-00089,,,,NoIndex,DatePalm_-_Date_Fruits,
3,DPWGS-00072,DPWGS-00072,,,,NoIndex,DatePalm_-_Date_Fruits,
4,DPWGS-00078,DPWGS-00078,,,,NoIndex,DatePalm_-_Date_Fruits,
5,DPWGS-00247,DPWGS-00247,,,,AGTACAAG,DatePalm_-_Date_Fruits,
5,DPWGS-00267,DPWGS-00267,,,,GACTAGTA,DatePalm_-_Date_Fruits,
6,DPWGS-00263,DPWGS-00263,,,,AGTCACTA,DatePalm_-_Date_Fruits,
6,DPWGS-00268,DPWGS-00268,,,,CAATGGAA,DatePalm_-_Date_Fruits,
7,32,32,,,,GACTAGTA,DatePalm_-_Date_Fruits,
7,DPWGS-00079,DPWGS-00079,,,,CTGAGCCA,DatePalm_-_Date_Fruits,
8,31,31,,,,NoIndex,DatePalm_-_Date_Fruits,
Status Report are below
Flowcell Summary
Clusters (Raw) Clusters(PF) Yield (MBases)
2,243,033,353 1,710,124,620 342,025
Lane Summary
Lane PF Clusters % of the % Perfect % One mismatch Yield (Mbases) % PF % >= Q30 Mean Quality
lane barcode barcode Clusters bases Score
1 0 46,813 74.81 75.65 33.00
2 0 40,294 64.81 72.67 32.12
3 0 46,675 91.71 87.04 35.26
4 0 13,543 26.86 53.72 27.30
5 244,751,056 100.00 97.46 1.88 48,950 84.95 79.86 33.46
6 237,309,355 100.00 72.61 25.73 47,462 91.76 87.45 35.40
7 243,656,285 100.00 92.56 6.93 48,731 90.96 86.39 35.19
8 0 49,557 83.13 80.02 33.
hello Ido Tamir,
Thank you for your reply.Yes I have removed Noindex into empty while converting the data.Report file is based on that changes.
NoIndex changed to empty while running the script
Hi All,
We have identified the problem.The above mentioned problem is happened due to File format of linux Server. Bcl2fast Version is working properly in XFS file system. But If we are using gpfs file system in Linux server,bcl2fastq V2 is generating partial out put file, missing R1 or both R1 and R2. We have contacted illumina and informed the same. They are internally checking the issue of Bcl2fast with gpfs file system.