Locus
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LAPD v.1.0
LAPD can estimate maximum likelihood allele. LAPD is a convenient, easy-to-use software specially designed to enable you to estimate maximum likelihood allele and two-locus haplotype frequencies, using an Expectation-Maximization algorithm,
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BayesAss v.1.0
Inference of recent migration rates between populations using multi-locus marker genotype data.
SAM tools v.0.1.9
Manage SAM files with this software. SSAM (Sequence Alignment/Map) format is a generic format for storing large nucleotide sequence alignments. SAM aims to be a format that: 1. Is flexible enough to store all the alignment information generated by
GGT (Graphical GenoTypes) v.2.0
View and edit molecular marker data with this tool. GGT (Graphical GenoTypes) is a graphical representation of molecular marker data can be an important tool in the process of selection and evaluation of plant material.
Euclide v.0.6.6
Euclide is a dynamic geometry software, which tries to be as flexible as possible. You start by placing some free points, then you create objects using these points: lines, circles, line segment, circle arcs...
FSTAT v.2.9.3.2
Gene diversities estimation made easy. FSTAT is a computer package for PCs which estimates and tests gene diversities and differentiation statistics from codominant genetic markers.
MSAnalyzer v.4.05
MSAnalyzer is a simple data analysis tool, microsatellite analyser (MSA): a platform independent analysis tool for large microsatellite data sets, can handle large microsatellite data sets. To avoid error prone reformatting,
Genevar v.2.0.1
Gene expression analysis made easy. Genevar integrate multiple datasets, and provides analysis and visualization of associations between sequence variation and gene expression in eQTL studies. Genevar allows researchers to investigate eQTL
DTscore v.1.0
DTscore is a distance based tamdem duplication tree reconstruction algorithm. It is based on a simple tandem duplication model, which assumes unequal recombination (crossover) as the only duplication mechanism.
ProtAnnot v.2.4 Build 6638
ProtAnnot is a small protein annotation viewer, displays protein annotations in the context of the genomic sequence.
SNVer v.0.0.2
Detection of rare and common variants in next generation sequencing. SNVer call common and rare variants in the analysis of pool or individual next-generation sequencing data. The software reports one single overall p-value for evaluating the