Recreating TCGA FASTQ file from BAM and unaligned files - How to randomize reads?

[methylnick]

BBmap can do that :
I haven't used it but it includes a tool to reorder reads while keeping pairs together

shuffle.sh in=R1.fastq in2=R2.fastq out=R1_rand.fastq out2=R2_rand.fastq

Thanks for that Micheal.Ante, this looks to be what I am looking for, fun times playing with it! cheers.

Nick

[methylnick]

Out of curiosity, in what context(s) does the order of reads in a FASTQ file matter? I could imagine in clustering or something like that...but most mappers treat reads independently right?

Also I was hoping to peform some saturation analysis so downsampling the FASTQ files and see what happens to the gene transcripts but also the unmapped stuff.

Good to know it does have an affect on de-novo assembly, which is also something I would like to try out.

cheers

Nick

[maubp]

Read order does matter for many de novo assemblers, and also for things like k-mer based normalisation.

[fanli]

Out of curiosity, in what context(s) does the order of reads in a FASTQ file matter? I could imagine in clustering or something like that...but most mappers treat reads independently right?

[Michael.Ante]

BBmap can do that :
I haven't used it but it includes a tool to reorder reads while keeping pairs together

shuffle.sh in=R1.fastq in2=R2.fastq out=R1_rand.fastq out2=R2_rand.fastq

[methylnick]

Hi fellow colleagues, I have been looking around the forum and google searching and it would seem my issue is a little obscure.

I am performing in-silico analysis of raw level 1 TCGA sequence reads and was hoping to generate "pseudo"-simulated FASTQ files. In the sense, that from the BAM file and unaligned FASTQ file from the same individual, I would like to recreate the full FASTQ file to replicate the TCGA pipeline and then test on some bespoke pipelines I am trying to get a handle on.

What I have done so far is:

1. use samtools bamshuf to randomise the BAM file.
2. convert the randomised BAM file to FASTQ.

This is where I am stuck because if I catenate this FASTQ file to the unaligned FASTQ files all I would get is the unaligned reads stacked right after all those within the BAM file.

Is there a tool out there that can randomize the order of sequence reads in a FASTQ file? And it would be for paired end data as well, hoping to preserve the paired ends at the same time?

Apologies if I had not refined my searches and there is something obvious available. I am hoping there is something short of learning a programming language and writing the script from scratch!!!

Cheers

Nick