This is a central and still controversial question in NGS analysis. What are duplicates and what to do about them (an introduction!) 8.1 Tools for analyzing time series RNA-Seq data ?.6.2 How much coverage do I need? - recent publications.6.1 additional Information from Wout (VIB Nucleomics core ).6 How much coverage do I need to ensure good quality results ?.5 How can I install FASTQ groomer as standalone (without installing GALAXY on my computer) ?.4 How does Illumina sequencing works on the chip ?.3.3 Which software do I use to analyze Nanopore sequences ?.3.2 Can I analyze variants with Nanopore ?.3.1 How much sample do I need for Nanopore ?.2 what is the base system used in my FastQ data (could be public data).1 what are duplicates and what to do about them (an introduction!).
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