A procedure to find Fst outliers based on an inferred distribution of neutral Fst
☆20Jun 9, 2026Updated 4 months ago
Alternatives and similar repositories for OutFLANK
Users that are interested in OutFLANK are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Multivariate vIsualisatioN and OuTlier Analysis Using R☆15Apr 8, 2023Updated 3 years ago
- ☆30Oct 14, 2022Updated 4 years ago
- ABLE - Approximate Blockwise Likelihood Estimation☆17Jul 4, 2018Updated 8 years ago
- Genetic Map Comparison☆20Nov 10, 2022Updated 3 years ago
- Process linked-read data, from raw sequences to phased haplotypes, batteries included. Works with WGS too!☆23Updated this week
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- Simple and flexible manipulation of genomic data.☆16Apr 16, 2025Updated last year
- Repository for the Data challenge about Software and Statistical Methods for Population Genetics (SSMPG 2017)☆14Sep 19, 2017Updated 9 years ago
- ☆15Jul 17, 2019Updated 7 years ago
- ☆16Aug 25, 2026Updated 2 months ago
- TEFLoN uses paired-end illumina sequence data to discover and genotype transposable elements present in your samples.☆14Mar 5, 2021Updated 5 years ago
- ☆16Mar 20, 2023Updated 3 years ago
- ☆16Jun 14, 2017Updated 9 years ago
- Tree reconstruction of ancestry using incomplete lineage sorting☆11Jan 9, 2026Updated 9 months ago
- Code and binaries related to processing haplotagging data☆16Mar 14, 2022Updated 4 years ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- Transfer coordinates across genomes☆23Jun 12, 2026Updated 4 months ago
- ☆13Aug 18, 2023Updated 3 years ago
- Calculate Hybrid Index and Heterozygosity from SNP data☆17Sep 2, 2025Updated last year
- seqqs is a C program/library for gathering quality statistics from sequencing data☆12May 12, 2014Updated 12 years ago
- Run and Analyse SLiM Population Genetics Forward Simulations from R.☆10Nov 26, 2025Updated 11 months ago
- Vignettes for Population Genetics in R☆26Aug 11, 2020Updated 6 years ago
- Population-scale detection of non-reference sequence variants using colored de Bruijn Graphs☆27Apr 29, 2024Updated 2 years ago
- ☆11Nov 22, 2024Updated last year
- Versatile tool for detecting selective sweeps with a variety of ages, strengths, starting allele frequencies, and completeness.☆15Feb 16, 2026Updated 8 months ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Obsolete!! Begin to turn to PrimerServer2☆10Jul 22, 2019Updated 7 years ago
- An R package to detect selection in biological pathways☆14Jan 19, 2024Updated 2 years ago
- microhaplotype visualizer and analyzer☆23Jun 24, 2021Updated 5 years ago
- Convert structural variants to sequence graphs [ VCF + FASTA ---> GFA ]☆11Mar 6, 2024Updated 2 years ago
- Scripts for reformatting data. Mainly from tab separated to an esoteric program specific format☆13Mar 19, 2026Updated 7 months ago
- R Package for performing Qst-Fst analyses☆21Nov 14, 2017Updated 8 years ago
- ☆11Jan 14, 2019Updated 7 years ago
- A Python package for landscape genomic simulation☆14Dec 15, 2025Updated 10 months ago
- Bioinformatics scripts for genome analysis☆17Oct 26, 2022Updated 4 years ago
- End-to-end encrypted email - Proton Mail • AdSpecial offer: 40% Off Yearly / 80% Off First Month. All Proton services are open source and independently audited for security.
- Pipeline for GTseq genotyping and quality control☆17Jan 30, 2023Updated 3 years ago
- Automated and Distributed Population Genetic Model Inference from Allele Frequency Spectra☆20Mar 31, 2026Updated 6 months ago
- mixture classification, constraint optimization, outlier detection, population structure, admixture history, and selection detection.☆91Jun 14, 2021Updated 5 years ago
- D Frequency Spectrum: Signatures of introgression across the allele frequency spectrum☆18Sep 19, 2020Updated 6 years ago
- Utilities for analyzing next generation sequencing data☆17Sep 28, 2018Updated 8 years ago
- A python framework for inferring demography from tracts of identity by state as reported in PLoS Genetics by Harris and Nielsen (2013)☆15Aug 1, 2013Updated 13 years ago
- The `awk` script to calculate population stats in VCF files: convenient, simple, flexible☆33Aug 18, 2026Updated 2 months ago