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I used fastp with some RNA-seq data, and found the detected adapter sequences are identical to some rRNA or mtRNA sequences.
For example:
Detecting adapter sequence for read1...
GTTCGATTCCTTCCTTTCTTATTTTACTTTTACATAGGTTGGTTCCTCGAATGTGTGATA
Detecting adapter sequence for read2...
CAAACTCATGCATATCACATAGTTAATCCAAGTCCATGACCATTAACTGGAGCCTTTTCA
When I run blast with these sequences, it says these sequences are 100% identical to mouse mtRNA.
It's that means the RNA-seq sample contain a lot of rRNA and mtRNA? Should I trim these sequences before mapping?
The text was updated successfully, but these errors were encountered:
Hi, developer
I used fastp with some RNA-seq data, and found the detected adapter sequences are identical to some rRNA or mtRNA sequences.
For example:
Detecting adapter sequence for read1...
GTTCGATTCCTTCCTTTCTTATTTTACTTTTACATAGGTTGGTTCCTCGAATGTGTGATA
Detecting adapter sequence for read2...
CAAACTCATGCATATCACATAGTTAATCCAAGTCCATGACCATTAACTGGAGCCTTTTCA
When I run blast with these sequences, it says these sequences are 100% identical to mouse mtRNA.
It's that means the RNA-seq sample contain a lot of rRNA and mtRNA? Should I trim these sequences before mapping?
The text was updated successfully, but these errors were encountered: