AI-sandbox / archetypal-analysisLinks
☆15Updated 2 years ago
Alternatives and similar repositories for archetypal-analysis
Users that are interested in archetypal-analysis are comparing it to the libraries listed below
Sorting:
- Genome-wide scan for balancing selection using beta statistic☆29Updated 2 years ago
- Likelihood-based Selective Sweep Detection☆40Updated 2 years ago
- A module for improving the insertion sequences of structural variant calls☆33Updated 4 years ago
- ☆44Updated last year
- Pipeline to detect PAVs (presence/absence variations) in genome comparison using whole genome alignment.☆29Updated 7 years ago
- ☆31Updated 6 years ago
- Integrate multiple genome assemblies into a pangenome graph☆35Updated 3 years ago
- Invertory of TE-gene isoforms☆13Updated 2 years ago
- A software package for local ancestry inference and haplotype phasing☆43Updated 2 years ago
- Convert RepeatMasker ".out" file into a gff3 with colors!!!☆24Updated 5 years ago
- Haplotype and population structure inference using neural networks.☆27Updated last year
- Inferring natural selection by comparative population genomic analysis across species☆25Updated 2 years ago
- The GitHub for CLUES2, a method for inferring and evaluating evidence for selection.☆16Updated 8 months ago
- A pipeline to use Lep-Map3 to create linkage maps and LepAnchor for anchoring and orienting genome assemblies with said linkage maps.☆14Updated 6 months ago
- ☆16Updated 6 years ago
- This is used to achieve haplotype-resolved assembly of tetraploid genomes using gamete sequencings☆12Updated 4 years ago
- Genealogical Estimation of Variant Age (GEVA)☆32Updated 4 years ago
- R package for comparing mixture solutions to similarity data, with a focus STRUCTURE like models to ChromoPainter palettes☆29Updated 6 years ago
- TideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain☆21Updated last year
- Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact (Illumina) reads.☆32Updated 3 years ago
- Repository for pipeline code☆26Updated last year
- Split-read pipeline for the identification of non-reference TE insertions with TSDs☆25Updated 5 years ago
- A tool to calculate ploidy levels from genotype likelihoods and coverage using Hidden Markov Models☆18Updated 3 years ago
- A Hi-C scaffolding method☆22Updated 4 years ago
- use variant nesting information to flter overlapping sites from vg deconstruct output☆31Updated 6 months ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- HaploSweep is a method for detecting and categorizing soft and hard selective sweeps based on haplotype structure.☆11Updated last year
- Sampling and manipulating genome-wide ancestral recombination graphs (ARGs)☆14Updated 2 years ago
- hot_scan is a free software to detect genomic regions unusually rich (hotspot) in a given pattern via scan statistics☆10Updated 12 years ago
- A method for measuring chromosome-specific telomere length from long reads☆22Updated last year