Assuming that we have by chance a FASTQ from a library that we do not know if was done with stranded or unstranded protocol - how to check this fact?
The library was most likely done as paired end with Tru Seq - whole transcript RNAseq.
A tool for counting antisense matches probably would do - what would you suggest? Meci!
The library was most likely done as paired end with Tru Seq - whole transcript RNAseq.
A tool for counting antisense matches probably would do - what would you suggest? Meci!
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