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Illumina Raw sequencing data conversion to single fastq file

I was given data in two formats, one in 18 fastq files separated as each pair end, and then raw data files in .txt that look like fastq file except without the .fastq at the end. I am trying to find the best way to convert these files to fastq.gz for use with basespace.

illumina fastq raw data rna-seq

2 answers

gzip [yourfile.fastq]

yields

[yourfile.fastq].gz

So all I need to do is add .fastq to then end and then gzip it? Also what is the best tool to demultiplex the data?

So all I need to do is add .fastq to then end and then gzip it? Also what is the best tool to demultiplex the data?

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