I am using a dataset for HiC analysis. The dataset is broken into 41 individual paired ended fastq files as the raw data.
I want to merge the 41 (x2) individual sam files after alignment but I want to do so without sorting the reads and maintaining the header intact.
Since this is HiC, the sequencing data is paired ended and I need to align each pair (_1 and _2) individually to the genome because the other end of the pair can be located anywhere else.
I am using the tool HiCexplorer to generate the contact matrices.
There is a mandatory requirement of using -reorder option for bowtie2 in this case.
If I use samtools merge, it will sort the input by default and this destroys the pair information (maintained in the order of reads in the input file in this case).
Any other ways to achieve the same ?
I could merge the fastq files before alignment by merging all the _1 files and the _2 respectively.
If I use the cat command that would presumably maintain the reads in the same order in both the _1 and _2 files individually and then proceed with the analysis. But I just want to find out if this can be achieved after alignment when I am sure that the -reorder option actually has been enforced while alignment equally on both ends of every pair of reads.