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The RNAseq data from GEO has multiple FASTQ files per pool. Each FASTQ file is around 14G (unzipped). Is it because of the SRA file size limit that you needed to split one FASTQ file per pool into multiple smaller ones?
When mapping with STAR, should I merge all FASTQ files within each pool?
Thank you,
Boxiang
The text was updated successfully, but these errors were encountered:
Dear Joseph, Jose, and colleagues,
The RNAseq data from GEO has multiple FASTQ files per pool. Each FASTQ file is around 14G (unzipped). Is it because of the SRA file size limit that you needed to split one FASTQ file per pool into multiple smaller ones?
When mapping with STAR, should I merge all FASTQ files within each pool?
Thank you,
Boxiang
The text was updated successfully, but these errors were encountered: