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.
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** Genotype_calling|Genotype calling | ** Genotype_calling|Genotype calling | ||
** SNP_calling|SNP Calling | ** SNP_calling|SNP Calling | ||
**tajima | |||
* Output | * Output | ||
** beagle_input|Beagle input files | ** beagle_input|Beagle input files | ||
Revision as of 14:17, 18 December 2012
- Pages
- Main_Page#Overview|Overview
- Download_and_installation|Installation
- Quick_start|Quick start
- Input|Input data
- change_log|Version log
- citing_angsd|Citing angsd
- authors|Authors
- Bugs | Bugs
- Summaries
- alleles_counts|Allele counts
- depth|Depth
- base_quality|Base quality
- Methods
- realSFS|SFS estimation
- Genotype_likelihoods_from_alignments|Genotypes likelihoods
- Inferring_Major_and_Minor_alleles|Major and Minor
- Error estimation|Error estimation
- Allele_Frequency_estimation|Allele frequencies
- Association|Association
- Genotype_calling|Genotype calling
- SNP_calling|SNP Calling
- tajima
- Output
- beagle_input|Beagle input files
- Glf_files|Genotype likelihood files
- filters | Filter output
- navigation
- mainpage|mainpage-description
- portal-url|portal
- currentevents-url|currentevents
- recentchanges-url|recentchanges
- randompage-url|randompage
- helppage|help
- SEARCH
- TOOLBOX
- LANGUAGES