TrimGalore
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A wrapper around Cutadapt and FastQC to consistently apply adapter and quality trimming to FastQ files, with extra functionality for RRBS data
Hi team I know that trimgalore is a wrapper around cutadapt but I want to check what I ran is considered fine I ran trimgalore to remove adaptors and primers...
Hi! I am trying to implement the following _cutadapt_ command using TrimGalore: ``` cutadapt -m 20 -O 20 -a "polyA=A{20}" -a "QUALITY=G{20}" -n 2 fastq_extracted/sample/R1.fastq.gz | cutadapt -m 20 -O...
Wondering if trimgalore can be used to cleanup mate-paired libraries? Is yes, is there a specific flag(s)?
Hello, I used trim-galore last year to clean up a lot of fastq.gz files I received from my service provider. It worked great and I was able to use the...
Hi Felix, We've recently analysed a paired-end 150 bp RRBS dataset, which ended having insert sizes well below 100 bp. This really concerned us, because insert size is having a...
Hello, trim_galore -o output --fastqc --paired $R1_file $R2_file I have utilized trim-galore to trim illumina adapters on my PE sequencing reads. When I tried to process the output fq files...
It seems like a good idea to pass on additional parameters to Cutadapt, e.g. `--poly-a`. In the current form, this can only be done via the `-a "SEQUENCE --additional_param" workaround,...
Hello I am working with human whole-genome bisulfite sequencing data, and paired-end reads. After using Trim Galore to remove adapters, I encountered an issue with the FastQC report for R2...
Relatively new to everything that isn't Windows I'm afraid.. can anyone help me out here? ``` (kraken2) martin@martin-VirtualBox:~$ mamba install -c bioconda trim-galore Looking for: ['trim-galore'] bioconda/linux-64 Using cache bioconda/noarch...
Hey, I am trying to trim pacbio sequencing data in a fastq file using trim galore. However, in every run trim galore gets stuck on the trimming step and never...