annovar_annotate_region | Annotate variant regions |
annovar_plink_conversion | Convert PLINK bim file to ANNOVAR input |
change_csv_locale | Changes delimiters in csv files |
check_command | Check if command exists |
compare_sets | Compare two vectors with simple set theory |
do_multirow | Combine rows with the same content |
dot-plink_fst | Internal Fst computation with PLINK |
dot-plink_pca | Internal PCA computation with PLINK |
ex2pdf | Generation of Exercise Sheets and Exams in PDF Format |
harmonize_genotypes | Genotype harmonization |
imbs | imbs. |
load_or_create_registry | Load or create a 'batchtools' registry |
manhattan_plot | Create a manhattan plot |
migrate_installed_packages | Migrate installed packages |
named_file_path | Named file path |
named_paste | Named paste |
plink_dedup | Remove duplicated variants |
plink_fst | Fst with PLINK |
plink_ld_pruning | LD pruning with PLINK |
plink_logistic | GWA (single variant logistic regression) with PLINK |
plink_marker_qc | Quality control on marker level with PLINK |
plink_merge | Merge two PLINK datasets |
plink_merge_list | Merge multiple PLINK datasets |
plink_normalize_vcf_conversion | Normalize and convert VCF files to PLINK binary files |
plink_pca | PCA with PLINK |
plink_rm_high_ld | Remove regions of high LD |
plink_rm_long_indels | Remove very long INDELS |
plink_sample_qc | Quality control on sample level with PLINK |
plink_sex_imputation | Sex imputation with PLINK |
plink_subset | Subset samples and variants using PLINK |
plink_vcf_conversion | Convert VCF files to PLINK binary files |
plink_write_ids | Write SNP or sample IDs to file |
print_3ptable | print_3ptable |
qw | Emulate Perl's 'qw' (quoted words) function |
read_sample | Read SNPTEST sample file |
system_call | Wrapper for 'system2' |
update_system2_job | update_system2_job |
vcf_normalization | Normalize VCF file to bi-allelic variants |
verbatimize | Verbatimize string |
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