Question: combining FASTQ files from 3 lanes
0
gravatar for Gabi
2.4 years ago by
Gabi • 0
Gabi • 0 wrote:

Hi,

I have data from multiple samples that were multiplexed and split across 3 lanes. These were demultiplexed by the sequencing facility, but I'm wondering how I can use galaxy to now merge the 3 FASTQ files that I have for each sample (ie. those that have the same barcode)?

Thanks

rna-seq multiplex galaxy • 1.6k views
ADD COMMENT • link • modified 2.4 years ago by Jennifer Hillman Jackson ♦ 25k • written 2.4 years ago by Gabi • 0
1
gravatar for Jennifer Hillman Jackson
2.4 years ago by
United States
Jennifer Hillman Jackson ♦ 25k wrote:

Hello,

Would the tool Text Manipulation: Concatenate work for you? There are other tools in the group NGS: QC and manipulation that will combine sequences together (merge first two, then merge that result with the third - in order), but if you just need to merge the files head to tail, then the first tool will do that.

Thanks, Jen, Galaxy team

ADD COMMENT • link written 2.4 years ago by Jennifer Hillman Jackson ♦ 25k
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