Tag Archives: NGS

BioPython musings

On my quest to improve my scripting skils I have just recently taken the Introduction to BioPython course at the VIB in Leuven. The course It was all very well organized and the Instructor,  Kristian Rother , was well prepared … Continue reading

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Calculating and plotting mapped reads – a simple R/shell script

As this is my first post I’ll start with something very simple I did recently. The problem is simple: “how many reads did does my deep-seq experiment have and how many were mapped to the genome?”. I am now dealing … Continue reading

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