I am download the fastq files for study GSE132802 through https://www.ebi.ac.uk/ena/browser/view/PRJNA549083. This is paired fastq file, but I only got one fastq file. I am considering split it. But I am not sure what is the best way to do it.
PRJNA* is a study identifier. There are a total of 14 samples. You will need to download each sample individually. Sample can be split correctly while it is being downloaded using sra-toolkit.
An example that downloads 1 read for one sample is shown below.
You will get three files per sample. File _1 is Illumina index. FIle _2 is cell barcode+UMI. File _3 is the RNA read.
Thank you!