A Boolean Algebra for Genetic Variants
☆12Mar 16, 2026Updated this week
Alternatives and similar repositories for algebra
Users that are interested in algebra are comparing it to the libraries listed below
Sorting:
- multi_tbx: a simple tool for indexing VCF files and extract variant records for variant data stored in multiple VCF files.☆10Jan 7, 2022Updated 4 years ago
- Tool suite for HGVS variant descriptions☆48Feb 23, 2026Updated 3 weeks ago
- add true-negative SVs from a population callset to a truth-set.☆15Jun 17, 2022Updated 3 years ago
- HGVS variant description extractor☆11Sep 14, 2020Updated 5 years ago
- GFA insert into GenomicSQLite☆49Jun 7, 2021Updated 4 years ago
- use the noise☆15Apr 15, 2020Updated 5 years ago
- ☆59Dec 12, 2023Updated 2 years ago
- Library for manipulating genomic variants and predicting their effects☆86Feb 16, 2026Updated last month
- Software for error-tolerant coding of information into DNA sequences using finite-state transducers.☆12Jan 8, 2017Updated 9 years ago
- Transfer HiFi read mappings from their own assembly contigs to a standard reference☆38Dec 30, 2025Updated 2 months ago
- Naive PCA for genotype data☆10Jul 27, 2016Updated 9 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Feb 16, 2018Updated 8 years ago
- Library for indexing VCF files for random access searches by rsID☆17Mar 2, 2026Updated 2 weeks ago
- ProSolo, variant calling from single cell DNA-seq data, or: bulk backing vocals for single cell solos.☆21Sep 1, 2021Updated 4 years ago
- Python package for cancer early detection based on a model of cancer evolution and circulating tumor DNA (ctDNA) shedding☆13Jan 8, 2021Updated 5 years ago
- Resource of human chromosome schematics & images☆95Sep 4, 2024Updated last year
- ☆102Apr 22, 2024Updated last year
- PGR-TK: Pangenome Research Tool Kit☆22Mar 13, 2025Updated last year
- Panache is a web-based interface designed for the visualization of linearized pangenomes. It can be used to show presence/absence informa…☆47Jun 7, 2023Updated 2 years ago
- 🧬 Viral genome reference alignment☆12Jan 26, 2021Updated 5 years ago
- Bam Read Index - Extract alignments from a bam file by readname☆28Apr 22, 2024Updated last year
- find likely coding segments in DNA using composition-normalised hexamer tables☆18Oct 18, 2024Updated last year
- ziglang + htslib☆21Oct 31, 2021Updated 4 years ago
- Singular Genomics Demultiplexing Tool☆16Mar 5, 2024Updated 2 years ago
- Tool (experimental) to compute layout from overlaps with spectral algorithm☆11Nov 28, 2017Updated 8 years ago
- CRISPR/Cas9 guide RNA Design☆24Feb 20, 2024Updated 2 years ago
- The Madeline 2.0 Pedigree Drawing Engine (PDE) is a pedigree drawing program designed to handle large and complex pedigrees with an empha…