The alignment of high-throughput reads is an important prerequisite for a lot of the recipes in this book, including RNAseq and SNP/INDEL calling. We looked at them in depth in Chapter 1, Performing Quantitative RNAseq, and Chapter 2, Finding Genetic Variants with HTS Data, but we didn't cover how to actually perform alignment. We wouldn't normally do this within R; the programs needed to make these alignments are powerful and run from the command line as independent processes. But R can control these external processes, so we'll look at how to run an external process so you can control them from within an R wrapper script, ultimately allowing you to develop end-to-end analysis pipelines.
Germany
Slovakia
Canada
Brazil
Singapore
Hungary
Philippines
Mexico
Thailand
Ukraine
Luxembourg
Estonia
Lithuania
Norway
Chile
United States
Great Britain
India
Spain
South Korea
Ecuador
Colombia
Taiwan
Switzerland
Indonesia
Cyprus
Denmark
Finland
Poland
Malta
Czechia
New Zealand
Austria
Turkey
France
Sweden
Italy
Egypt
Belgium
Portugal
Slovenia
Ireland
Romania
Greece
Argentina
Malaysia
South Africa
Netherlands
Bulgaria
Latvia
Australia
Japan
Russia