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The first deep learning based Nanopore simulator which can simulate the process of Nanopore sequencing.

C 115 40 Updated Oct 20, 2020

simON-reads ("Simulate Oxford Nanopore Reads") is a simple yet powerful tool to generate fastq files containing MiniON-like long reads

Python 2 Updated Apr 8, 2024

Nanopore sequence read simulator

Python 230 56 Updated Sep 10, 2024

NanoSim-H: a simulator of Oxford Nanopore reads; a fork of NanoSim.

Python 17 6 Updated Sep 7, 2022

Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and Oxford Nanopore ultra-long reads.

Python 281 27 Updated Sep 10, 2024

Tools for plotting methylation data in various ways

Python 125 10 Updated Aug 13, 2024

Structural variant caller for real-time long-read sequencing data

Python 51 6 Updated Dec 1, 2022

GUI/CommandLine Tool Box for biologistists to utilize NGS data.

Shell 885 187 Updated Sep 1, 2024

Oxford Nanopore's Basecaller

C++ 479 59 Updated Aug 1, 2024

DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets

Python 34 2 Updated Feb 25, 2021

Haplotype aware de novo assembly of diploid genome from long reads

C++ 53 11 Updated Mar 16, 2022

Read-based phasing of genomic variants, also called haplotype assembly

Python 332 38 Updated Sep 4, 2024

Generate an interactive dot plot from mummer or minimap alignments

HTML 188 53 Updated Jan 17, 2024

Dotplot large Genomes in an Interactive, Efficient and Simple way

JavaScript 96 12 Updated Mar 20, 2024

Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing

Java 32 4 Updated Jun 28, 2024

H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)

Python 68 9 Updated Oct 28, 2020

Genome assembly evaluation tool

AMPL 394 76 Updated Jun 19, 2024

De novo assembly from Oxford Nanopore reads.

C++ 68 10 Updated Sep 10, 2024

[MOVED] Moved to paoloshasta/shasta. De novo assembly from Oxford Nanopore reads

C++ 270 58 Updated Oct 13, 2022

Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations

Java 633 379 Updated Sep 10, 2024

Toolset for SV simulation, comparison and filtering

C++ 349 46 Updated Dec 1, 2023

Long read based human genomic structural variation detection with cuteSV

Python 242 36 Updated May 31, 2024

Structural variation caller using third generation sequencing

Python 544 91 Updated Aug 13, 2024

An overview of all nanopack tools

Python 207 14 Updated Jun 2, 2023

Plotting scripts for long read sequencing data

Python 413 48 Updated Jun 19, 2024

Copy number variant detection from targeted DNA sequencing

Python 540 164 Updated Sep 4, 2024

a Shiny/R application to view and annotate copy number variations

R 28 12 Updated Mar 8, 2023

Tool for finding matches to degenerate sequence motifs in FASTA files.

Python 12 5 Updated Mar 11, 2024

A genome-scale, fast, and precise segmental duplications mapping tool

Rust 31 5 Updated Sep 6, 2024

Uniform Manifold Approximation and Projection

Python 7,352 799 Updated Aug 18, 2024
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