Closed huwenhuo closed 10 months ago
I have similar issue, I downloaded data from EBI that only have two fastq.gz files (R1 and R2), I renamed them as suggested (A1_S1_L001_R1_001.fastq.gz, A1_S1_L001_R2_001.fastq.gz), but still can not run cellranger, could anybody help me? Many thanks!
I have an error showing that FASTQ header mismatch detected
I have a similar problem, perhaps the following forum can help: https://forum.qiime2.org/t/how-to-determine-whether-fastq-files-are-already-demultiplexed/13997
I somehow got only R1 and R2 fastq files after submitted as Amplicon-Seq. How can I convert these two files of R1/R2 fastq to I1, R1, R2 three fastq files using cell ranger?