Dear all
im trying to trim paired-end RRBS illumina reads using Trim galore. as far as i understood, paired end reads must be trimmed...
6 results in 0.0021 seconds.
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trimming paired end reads using Trim galore
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5' Kmers problem with whole genome re-sequencing data
Hi all,
I am having some issues with getting rid of kmers in my sequencing data sets. We have re-sequenced several African buffalo genomes... -
Adapter_and_kmer_trimming
Hi everyone,
I am using publicly available, 51 bp paired-end RNA seq data and I have some questions concerning the quality trimming of... -
Struggling with quality trimming
Hello everybody,
this is my first try to trim Illumina (paired-end) reads on the unix command line.
If i get it correctly, de-multiplexing... -
Do I need to run trim galore even if my reads are of good quality?
Hi,
I am a beginner in the field of genomics. So I have one doubt should I use trim galore to trim my sequence even if they are of good... -
How to integrate Trim Galore in Galaxy?
Hello. I have downloaded and installed Trim Galore in my local machine. Now I want to integrate it into Galaxy. I know the procedure to add tool into...
