ANGSD: Analysis of next generation Sequencing Data
Latest tar.gz version is (0.938/0.939 on github), see Change_log for changes, and download it here.
ANGSD: Difference between revisions
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Latest version is 0. | Latest version is 0.577, see [[Change log]] for changes, and download it [[Download and installation | here]]. | ||
The program is developed on tested on a Linux system with gcc compiler. It compiles on OSX with clang, but OSX is not really that tested. | The program is developed on tested on a Linux system with gcc compiler. It compiles on OSX with clang, but OSX is not really that tested. | ||
Revision as of 13:54, 16 January 2014
Latest version is 0.577, see Change log for changes, and download it here.
The program is developed on tested on a Linux system with gcc compiler. It compiles on OSX with clang, but OSX is not really that tested.
There is a (very) short Quick Start, which contains a test data set you can download, and will contain some useful examples.
About
ANGSD is a software for analyzing next generation sequencing data. The software can handle a number of different input types from mapped reads to imputed genotype probabilities. Most methods take genotype uncertainty into account instead of basing the analysis on called genotypes. This is especially useful for low and medium depth data. The software is written in C++ and has been used on large sample sizes.
This program is not for manipulating '.bam' files, but solely a tool to perform various kinds of analysis. We recommend the excellent program SAMtools for outputting and modifying bamfiles.
Synopsis
./angsd [OPTIONS]
example of allele frequency estimated from genotype likelihoods with bam files as input using 10 threads
./angsd -out outFileName -bam bam.filelist -GL 1 -doMaf 1 -doMajorMinor 1 -nThreads 10