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DATAOPS-716 Use customized list of adapters, FastQC (#60)
* Use customized list of adapters, FastQC When hoovering over the adapter content plot in the the FastQC output displayed in the end of all seqreports the name of the adapter found is appearing. The adapters and names used are by default the ones specified in the FastQC software. However, the provided list is outdated and many of the adapters are used in several library preparation kits. A customized list can now be used as input instead to look for adapters we use at SNP&SEQ and to display relevant names when found. Files changed: - New file, adapter_list_fastqc.txt, added in config/tool_config/ to specify the adapters to look for. - The fastqc command in main.nf is now updated with the additional a-flag that is used to specify the use of the file described under the previous point. * Update config/tool_config/adapter_list_fastqc.txt Co-authored-by: Matilda Åslin <matilda.aslin@medsci.uu.se> * Update config/tool_config/adapter_list_fastqc.txt Co-authored-by: Matilda Åslin <matilda.aslin@medsci.uu.se> * Fixed indentation and permalink --------- Co-authored-by: Matilda Åslin <matilda.aslin@medsci.uu.se>
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# This file is copied and modified from | ||
# https://github.com/s-andrews/FastQC/blob/1faeea0412093224d7f6a07f777fad60a5650795/Configuration/adapter_list.txt | ||
# The file has been modified according to | ||
# https://knowledge.illumina.com/library-preparation/general/library-preparation-general-reference_material-list/000001314 | ||
# | ||
# This file contains a set of sequence fragments which will be explicitly | ||
# searched against your library. The reporting will be similar to the | ||
# Kmer plot, except that every sequence in this list will be shown so | ||
# you can use this to judge the level of adapter read-through even if those | ||
# adapter sequences aren't picked out by the Kmer module. | ||
# | ||
# Since every sequence here will be analysed and the results plotted it | ||
# doesn't make any sense to include duplicate sequences, or to add too | ||
# many sequences since your plot will end up a mess. | ||
# | ||
# You can add more sequences to the file by putting one line per entry | ||
# and specifying a name[tab]sequence. If the contaminant you add is | ||
# likely to be of use to others please consider sending it to the FastQ | ||
# authors, either via a bug report at www.bioinformatics.babraham.ac.uk/bugzilla/ | ||
# or by directly emailing simon.andrews@babraham.ac.uk so other users of | ||
# the program can benefit. | ||
# | ||
# For the time being it's going to be easier to interpret this plot if all | ||
# of the sequences provided are the same length, so we've gone with 12bp | ||
# fragments for now. | ||
|
||
Illumina TruSeq Adapter AGATCGGAAGAG | ||
Illumina TruSeq Small RNA Adapter TGGAATTCTCGG | ||
Illumina Stranded Total RNA Prep CTGTCTCTTATA | ||
PolyA AAAAAAAAAAAA | ||
PolyG GGGGGGGGGGGG |
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../../config/tool_config/adapter_list_fastqc.txt |