HI, I am trying to figure out if my transcriptomic data (downloaded from ncbi) was made using strand or non strand method. This information was not provided alongside the download page. Is there a way I can do this using the fastq file? Thanks
HI, I am trying to figure out if my transcriptomic data (downloaded from ncbi) was made using strand or non strand method. This information was not provided alongside the download page. Is there a way I can do this using the fastq file? Thanks
Use infer_experiment.py
from RSeQC after you align the data : RSeQC Output from infer_experiment.py - what does it mean?
You could quantify your data against a reference transcriptome with salmon
and use the library type to automatic detection -l A
. It will tell you then the most likely library type. Did you check the publication (if there is one) towards the method section / kit they used?
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You can align it as a stranded library and look at the alignments on a genome browser. If the library was actually unstranded, you will see a roughly 50/50 split between the strands in the alignments at any given location/gene, but if the library was stranded then you will see a strong bias towards the strand that the gene is on.