deML. Maximum likelihood demultiplexing
52gargammel. gargammel is an ancient DNA simulator
39leeHom. Bayesian reconstruction of ancient DNA fragments
31glactools. command-line tools for the management of genotype likelihoods and allele counts
30vgan. Suite of tools for pangenomics built using vg
25schmutzi. Maximum a posteriori estimate of contamination for ancient samples
25ROHan. Joint inference of heterozygosity rates and runs of homozygosity
23freeIbis. An efficient basecaller for Illumina sequencers with calibrated quality scores
9BCL2BAM2FASTQ. C++
6SAFARI. Sensitive Alignments from a RYmer Index
6aLib. Python
3dice. Joint estimate of demography and contamination for nuclear ancient DNA
3DNA2INT. quick benchmarking to check the best way to transform DNA letters to integers
3VCFparser. C++ library for parsing VCF files
3mappability_snpable. Shell
2baselengthFilter. This program reads a BAM and produces another with a length filter applied on reads
2trieFinder. The trieFinder program is designed to rapidly map Digital Gene Expression (DGE) tags of various lengths to RefSeq, UniGene, and/or genomic sequences. It annotates the tags with information from the sequence files, providing output in a format that is amenable to both transcript quantification and the detection of novel transcripts.
2bam2prof. the subprogram in schmutzi but rewritten using htslib
2insertsize. Simple C++ program built using samtools to get the insert size from BAM files
2cinch. Python
2libgab. A C++ class of useful little functions
1GenStat. C++
1mitochondrialSimulator. A simple mitochondrial simulator
1aligneur_sequence. C++
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