mengqvist / DNApyLinks
Code for DNA plasmid editing.
☆43Updated 6 years ago
Alternatives and similar repositories for DNApy
Users that are interested in DNApy are comparing it to the libraries listed below
Sorting:
- Biological Graphic tool in Python☆34Updated 5 years ago
- Efficient handling of FASTQ files from Python☆51Updated this week
- A software for the multispecies design of CRISPR/Cas9 libraries☆36Updated 2 years ago
- Validate FastQ Files☆36Updated 6 years ago
- http://www.combio.pl/alfree☆23Updated 3 years ago
- Library for manipulating genomic variants and predicting their effects☆84Updated last year
- Tool package to perform in-silico CRISPR analysis and assessment☆29Updated last year
- Tandem Repeat Annotation Library☆25Updated 2 years ago
- ☆37Updated 3 months ago
- Tools for next-generation sequencing analysis☆88Updated 6 years ago
- fast, memory-efficient, pythonic (and command-line) access to fasta sequence files☆87Updated 7 years ago
- A Python package for Biopython that gives feature annotations from GenBank records a new and better life☆14Updated 9 years ago
- Interactive, web-based BLAST results visualization tool. Accessible at https://kablammo.wasmuthlab.org.☆68Updated 2 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆40Updated 4 years ago
- Find common blocks and differences between DNA sequences☆42Updated 4 months ago
- What's The Function of these genes?☆22Updated 8 years ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 7 years ago
- 🧬 MSABrowser: dynamic and fast visualization of sequence alignments, variations, and annotations☆33Updated last year
- small RNA analysis from NGS data☆37Updated 11 months ago
- MIRROR OF: The European Molecular Biology Open Software Suite (from git://anonscm.debian.org/debian-med/emboss.git)☆27Updated 3 years ago
- Demonstrating best practices for bioinformatics command line tools☆26Updated 5 years ago
- A Python module to analyze Sanger sequencing results.☆25Updated last year
- ☆38Updated 5 months ago
- An easy-to-use way for running Galaxy workflows.☆20Updated 5 years ago
- Module for reading ABI Sanger sequencing trace files☆40Updated 9 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 7 months ago
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- Docker image of JBrowse Genome Browser☆16Updated 4 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆52Updated 7 years ago