fgvieira / ngsLDLinks
Calculation of pairwise Linkage Disequilibrium (LD) under a probabilistic framework
☆47Updated 2 years ago
Alternatives and similar repositories for ngsLD
Users that are interested in ngsLD are comparing it to the libraries listed below
Sorting:
- R Package to Estimate Variable Recombination Rates using Population Genetic Data☆43Updated 6 years ago
- Framework for analyzing low depth NGS data in heterogeneous populations using PCA.☆56Updated 5 months ago
- Read, manipulate and visualize 'Pairwise mApping Format' data in R☆76Updated 4 years ago
- Estimate recombination rates from population genetic data☆70Updated 5 years ago
- Pipelines and tools for the processing of ancient and modern HTS data.☆47Updated last month
- Methods for examining PCA locally along the genome.☆86Updated last year
- Infer demographic history with the Moran model☆50Updated 5 months ago
- A statistical framework for ploidy estimation using NGS short-read data☆62Updated 7 years ago
- Tools and Utilities for msmc and msmc2☆49Updated 4 months ago
- ☆65Updated 3 years ago
- A pipeline that accepts a VCF file to run through Admixture☆63Updated 11 months ago
- SelectionHapStats is a repository of Python scripts written to identify natural selection events in the genome and R scripts written to v…☆27Updated 7 years ago
- Population genetics analyses from NGS data☆25Updated 4 years ago
- A method for variant graph genotyping based on exact alignment of k-mers☆87Updated 6 years ago
- predicting DFE and alpha from polymorphism data☆28Updated 7 years ago
- ☆24Updated 8 years ago
- Tutorial on using popular tools for learning about population history☆52Updated 7 years ago
- findGSE is a tool for estimating size of (heterozygous diploid or homozygous) genomes by fitting k-mer frequencies iteratively with a ske…☆38Updated last year
- Genealogical Estimation of Variant Age (GEVA)☆31Updated 4 years ago
- ☆31Updated 2 years ago
- Evaluate variant calls and its combination with k-mer multiplicity☆67Updated 3 years ago
- ✏️ Genome assembly polishing & SNV detection☆71Updated 2 months ago
- QUILT: Low coverage whole genome sequence imputation with large reference panels☆65Updated last month
- Efficient program for calculating Extended Haplotype Homozygosity (EHH) and Integrated Haplotype Score (iHS)☆45Updated 6 years ago
- Sampling and inference of genealogies with recombination☆46Updated 5 months ago
- A set of workflows written in Nextflow for Genome Annotation.☆46Updated last year
- ☆44Updated 8 months ago
- Pinpoints the mutation favored by selection☆34Updated 4 years ago
- A EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment☆87Updated 4 years ago
- Scripts to estimate genome size and coverage from kmer distribution generated by jellyfish☆57Updated 2 years ago