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  • Queen Mary University of London
  • London, UK

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Starred repositories

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Snakemake workflows for performing whole genome alignment with Cactus efficiently on SLURM clusters

Python 9 2 Updated Feb 27, 2026

TOGA2: A faster, more versatile successor of Tool to infer Orthologs from Genome Alignments

C 32 2 Updated Apr 8, 2026

base-accurate DNA sequence alignments using WFA and mashmap3

C++ 214 25 Updated Mar 20, 2026

Pairwise whole genome aligner

C 234 16 Updated Mar 2, 2026

Fast Tandem Repeat Finder

C 16 2 Updated Mar 9, 2026

Portable solution to generate genome alignment chains using lastz

Python 64 16 Updated Apr 6, 2026

BUSCO_Phylogenomics | Pipeline to construct species phylogenies using BUSCO proteins

Python 98 15 Updated Mar 7, 2026

Fast genomics quality control tools for sequencing data, written in Rust.

Rust 76 3 Updated Apr 8, 2026

Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data

C++ 177 50 Updated Aug 22, 2024

Evaluate variant calls and its combination with k-mer multiplicity

C 68 7 Updated Dec 2, 2022

lumpy: a general probabilistic framework for structural variant discovery

C 342 115 Updated Feb 22, 2026

Genome Interval Arithmetic in R

R 95 24 Updated Jan 11, 2026

Collection of low-level functions for working with vctrs

R 36 7 Updated May 11, 2022

Tidy Plots for Scientific Papers

R 678 30 Updated Mar 31, 2026

The web framework for content-driven websites. ⭐️ Star to support our work!

TypeScript 58,249 3,325 Updated Apr 8, 2026

Finding Recurrent Substitutions in Multiple Sequence Alignments

Python 6 Updated Feb 6, 2026

Tool for drawing gene structures from genome annotation files.

Python 22 2 Updated Mar 5, 2026

Genome alignment and synteny plots

R 34 5 Updated Mar 24, 2026

The SYNY pipeline investigates synteny between species by reconstructing protein clusters from gene pairs.

Perl 52 3 Updated Feb 8, 2026

Structural variation and indel detection by local assembly

C++ 255 49 Updated Apr 8, 2026

A tutorial on structural variant calling for short read sequencing data

R 42 3 Updated Oct 24, 2024

High Performance GWAS Plotting and Annotation

R 8 Updated Feb 25, 2026

Runs a combination of tools to generate structural variant calls on whole-genome sequencing data

Python 49 10 Updated Jun 2, 2020

a tool for CNV discovery and genotyping from depth-of-coverage by mapped reads

C++ 234 67 Updated Feb 17, 2022
Python 35 3 Updated Aug 18, 2024

A set of ready to use Agent Skills for research, science, engineering, analysis, finance and writing.

Python 17,724 1,955 Updated Apr 3, 2026

A scientific plotting library in Rust

Rust 670 20 Updated Apr 8, 2026

Phylogenetic orthology inference for comparative genomics

Python 116 8 Updated Apr 2, 2026

Synteny and Rearrangement Identifier

Cython 458 46 Updated Mar 17, 2026
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