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Tags: RNA-seq
umi-tools extract:
Flexible removal of UMI sequences from fastq reads.
UMIs are removed and appended to the read name. Any other barcode, for example a library barcode, is left on the read. Can also filter reads by quality or against a whitelist (see above)
The remaining commands, group, dedup and count/count_tab, are used to identify PCR duplicates using the UMIs and perform different levels of analysis depending on the needs of the user. A number of different UMI deduplication schemes are enabled - The recommended method is directional.
umi-tools dedup:
Groups PCR duplicates and deduplicates reads to yield one read per group
Use this when you want to remove the PCR duplicates prior to any downstream analysis
Introducing BBSplit: Read Binning Tool for Metagenomes and Contaminated Libraries
Removal of genome contaminants (BBSplit)
Removal of ribosomal RNA
StringTie for Transcript assembly and quantification
Extensive quality control:
The preseq package is aimed at predicting and estimating the complexity of a genomic sequencing library,
Herpes-virus is double-stranded RNA.
Herpes-simplex-Viren (humane Herpesviren Typ 1 und 2) sind häufige Ursachen rezidivierender Infektionen mit Beteiligung von Haut, Mund, Lippen, Augen und ...
Salmon used expectation–maximization (EM) algorithm to assign reads if two copy of genes occurs.
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Preparing a GTF file from GenBank for bacterial RNA-seq analysis, using the example of WA
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