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Documentation of the Snakemake-Workflows project

155 25 Updated Feb 2, 2022

DeepMod: a deep-learning tool for genomic-scale, strand-sensitive and single-nucleotide based detection of DNA modifications

Python 104 35 Updated Mar 8, 2023

Oxford Nanopore Technologies fast5 API software

Python 154 29 Updated Feb 27, 2024

Dotplot large Genomes in an Interactive, Efficient and Simple way

JavaScript 103 13 Updated Jan 7, 2025
C 71 18 Updated Apr 28, 2020

Tombo is a suite of tools primarily for the identification of modified nucleotides from raw nanopore sequencing data.

Python 233 54 Updated May 4, 2023

Detecting methylation using signal-level features from Nanopore sequencing reads

Python 115 21 Updated Jun 4, 2023

Synteny Mapping and Analysis Program

Java 26 7 Updated Jun 1, 2025

Pore-C support

Python 53 6 Updated Feb 22, 2023

A tool to map bisulfite converted sequence reads and determine cytosine methylation states

HTML 422 108 Updated Apr 22, 2025

A comparison of different Oxford Nanopore basecallers

Python 316 52 Updated Aug 5, 2019

A high performance and compression ratio compressor for genomic data, powered by GTXLab of Genetalks.

170 40 Updated Apr 18, 2022

Python library to facilitate genome assembly, annotation, and comparative genomics

Python 825 191 Updated Jun 5, 2025

Guided synteny alignment between duplicated genomes (within specified quota constraint)

Python 58 20 Updated Sep 5, 2017

CoGe (Comparative Genomics) Platform

Perl 44 22 Updated Dec 21, 2021

Scientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments

Scala 1,019 366 Updated Jun 4, 2025

VIM Configuration for Python / Cython / C Development

Vim Script 655 340 Updated Mar 18, 2021

A cross-platform and ultrafast toolkit for FASTA/Q file manipulation

Go 1,413 166 Updated Apr 25, 2025

Genome annotation with AUGUSTUS

C++ 304 113 Updated Jan 6, 2025

Signal-level algorithms for MinION data

C++ 586 161 Updated Aug 5, 2023

Training models for basecalling Oxford Nanopore reads

Python 115 43 Updated Jan 13, 2022

3D de novo assembly (3D DNA) pipeline

Shell 212 56 Updated Nov 29, 2023

A versatile pairwise aligner for genomic and spliced nucleotide sequences

C 1,974 435 Updated Jun 4, 2025

bedtools - the swiss army knife for genome arithmetic

C 980 292 Updated Mar 11, 2025

Long read alignment analysis. Generate a reports on sequence alignments for mappability vs read sizes, error patterns, annotations and rarefraction curve analysis. The most basic analysis only requ…

Python 47 10 Updated Aug 27, 2018

Bayesian haplotype-based genetic polymorphism discovery and genotyping.

C++ 832 265 Updated May 31, 2025

Generate an interactive dot plot from mummer or minimap alignments

HTML 202 58 Updated Jan 17, 2024

A simple and fast metassembler and assembly gap filler designed for long molecule based assemblies.

C++ 204 33 Updated Nov 18, 2022

MUMmer3

C++ 17 9 Updated Jan 12, 2022
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