| Package Name | Access | Summary | Updated |
|---|---|---|---|
| pdivas | public | PDIVAS: Pathogenicity predictor of Deep-Intronic Variants causing Aberrant Splicing | 2025-04-22 |
| cpc2 | public | Coding Potential Calculator 2 (CPC2) | 2025-04-22 |
| nrpys | public | Python language bindings for nrps-rs substrate specificity predictor. | 2025-04-22 |
| annonars | public | Genome annotation based on Rust and RocksDB. | 2025-04-22 |
| matchmsextras | public | Additional network analysis functions for matchms | 2025-04-22 |
| panfeed | public | Compute gene-cluster specific k-mers over a pangenome | 2025-04-22 |
| callingcardstools | public | An API and collection of cmd line tools to work with calling cards sequencing data | 2025-04-22 |
| methphaser | public | MethPhaser: methylation-based haplotype phasing of human genomes | 2025-04-22 |
| hificnv | public | Copy number variant caller and depth visualization utility for PacBio HiFi reads | 2025-04-22 |
| r-ccqtl | public | CCQTL is a wrapper around the R/qtl2 (Broman et al, Genetics 2019 10.1534/genetics.118.301595) functions, with hard-coded parameters tailored for QTL mapping in the Collaborative Cross. | 2025-04-22 |
| quickbam | public | Parallel BAM file access API for high throughput sequence analysis informatics | 2025-04-22 |
| brawn | public | A tool for handling repetitive insertions into sequence alignments. | 2025-04-22 |
| mgems | public | mGEMS - sequencing data binning based on probabilistic classification | 2025-04-22 |
| wgd | public | wgd v2: a suite of tools to uncover and date ancient polyploidy and whole-genome duplication | 2025-04-22 |
| rmats-long | public | rMATS-long is an integrated computational workflow for long-read RNA-seq data | 2025-04-22 |
| deeplcretrainer | public | Evaluating DeepLC performance and retraining prediction models. | 2025-04-22 |
| braker3 | public | BRAKER3 is the latest pipeline in the BRAKER suite | 2025-04-22 |
| hiphase | public | Small and structural variant phasing tool for PacBio HiFi reads | 2025-04-22 |
| seqverify | public | Seqverify analyzes whole genome sequencing data for gene-editing verification. | 2025-04-22 |
| fununifrac | public | A repository to implement UniFrac, but on functional profiles of metagenomic data. | 2025-04-22 |
| spagrn | public | A comprehensive tool to infer TF-centered, spatial gene regulatory networks for the spatially resolved transcriptomics (SRT) data. | 2025-04-22 |
| crussmap | public | crussmap is a faster tool to convert genome coordinates between difference reference assemblies. | 2025-04-22 |
| minibusco | public | minibusco: a faster and more accurate reimplementation of BUSCO | 2025-04-22 |
| perl-bio-phylo-forest-dbtree | public | DBIx::Class-backed, Bio::Phylo-like API for large phylogenies. | 2025-04-22 |
| t1dgrs2 | public | Generate a Type 1 Diabetes Genetic Risk Score (T1D GRS) that accounts for interactions between HLA DR-DQ risk haplotypes. | 2025-04-22 |
