overrepresented sequences in fastqc
I got the dataset from an already published paper after doing fastqc it showed overrepresented sequences. Please suggest a command line for the same.
• 908 views
•
link
updated
by
Ram
•
written
by
lonekaisar72 •
•
written
by
lonekaisar72 •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
How to give the defined p value in MACS2 command line (peak calling)
written by lonekaisar72 •
-
mirdeep2- unable to extract files for mapping -extract_miRNAs: command not found error
written by Supernova •
-
paired end reads cutadapt
written by anna •
-
Overrepresented % different between PE reads
written by Illinu
-
Filtering rRNA contamination (indicated by GC content plots) from RNA-seq data
written by tryingmybest •
-
FastQC report: Why no error in 'Adapter content' and which sequences of 'Overrepresented sequences'…
written by salamandra
-
trim adaptors RNA-seq
written by sophialovechan •
-
trim adaptors RNA-seq
written by sophialovechan •
-
Possible adapter on the forward sequence,
written by fkm.022 •
-
Trimming paired end RNA-seq with Trimmomatic
written by samantha_jeschonek
Cannot be answered because you show nothing.
How To Ask Good Questions On Technical And Scientific Forums
also: How to give the defined p value in MACS2 command line (peak calling)