Python library for primer-based verification of DNA assemblies: primer selection, data analyis, etc.
☆33Apr 9, 2025Updated 11 months ago
Alternatives and similar repositories for Primavera
Users that are interested in Primavera are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- 💫 Computer-aided DNA assembly validation and identification from restriction digests.☆15May 29, 2025Updated 9 months ago
- Predict DNA assembly clone validity rates - powered by Kappa☆10Jul 24, 2020Updated 5 years ago
- Batch domestication of genetic parts with Python☆16May 12, 2025Updated 10 months ago
- Find common blocks and differences between DNA sequences☆42Nov 5, 2025Updated 4 months ago
- A route planner for DNA assembly☆36May 12, 2025Updated 10 months ago
- Open source password manager - Proton Pass • AdSecurely store, share, and autofill your credentials with Proton Pass, the end-to-end encrypted password manager trusted by millions.
- Simple cloning simulator (Golden Gate etc.) for single and combinatorial assemblies☆66May 12, 2025Updated 10 months ago
- Draw genetic elements with HTML & CSS☆17Feb 8, 2017Updated 9 years ago
- 🏖️ The EGF Collection of Useful Bio Apps - Web demos of EGF software☆20Dec 10, 2022Updated 3 years ago
- 🎨 Python library to plot multi-part genetic constructs☆26Apr 9, 2025Updated 11 months ago
- 🤖 Python biolab automation library: parsers, report generators, picklist simulators, and more☆46May 29, 2025Updated 9 months ago
- DNA overhang misannealing data for Python☆13May 15, 2025Updated 10 months ago
- Short overhangs design for DNA assembly☆15Jun 8, 2022Updated 3 years ago
- Easily download genomes and build BLAST/Bowtie indexes in Python☆22Sep 30, 2022Updated 3 years ago
- Generate identicons for DNA sequences with Python☆38May 8, 2025Updated 10 months ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Toolkit for Modelling and Simulation of Gene Expressions and Metabolism☆13Jan 9, 2026Updated 2 months ago
- A versatile DNA sequence optimizer☆265Nov 5, 2025Updated 4 months ago
- abi2fastq is a small utility to convert Sanger sequencing reads in .abi (applied biosystems) format to FASTQ☆11Sep 19, 2017Updated 8 years ago
- Core library and basic plug-ins for the Amyris Genotype Specification Language (GSL) compiler.☆24Apr 5, 2023Updated 2 years ago
- An amino acid sequence annotator☆17May 15, 2025Updated 10 months ago
- Automated Sanger Analysis Pipeline (ASAP): a tool for rapidly analyzing Sanger sequencing data with minimum user interference.☆25Feb 13, 2025Updated last year
- Efficiently keep track of changes to genomes☆38Jul 22, 2024Updated last year
- Python library to plot DNA sequence features (e.g. from Genbank files)☆683Jul 2, 2025Updated 8 months ago
- ☆16Feb 19, 2026Updated last month
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Cello v2 is the continuation of the Cello genetic circuit design software.☆68May 16, 2022Updated 3 years ago
- Sequencing analysis pipeline☆15Dec 12, 2025Updated 3 months ago
- 👓 Python library to parse Snapgene *.dna files to dict or biopython seqrecord.☆30May 10, 2025Updated 10 months ago
- General low-level API☆50Jul 18, 2022Updated 3 years ago
- in silico plasmid extraction☆13Sep 18, 2017Updated 8 years ago
- Web based Registry platform for managing synthetic biological parts☆42May 16, 2024Updated last year
- This project contains simple methods to measure sample relatedness and identify potential swaps and contamination☆10Jan 8, 2016Updated 10 years ago
- Module for reading ABI Sanger sequencing trace files☆40Jun 15, 2016Updated 9 years ago
- Confirming specific taxonomic groups within your samples.☆19Dec 21, 2020Updated 5 years ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- C++ implementation of SBOL 2.3.2☆17Oct 13, 2020Updated 5 years ago
- Classify sequencing reads using MinHash.☆48Apr 6, 2020Updated 5 years ago
- Pathogenicity prediction of bacterial genomes☆17Jun 27, 2018Updated 7 years ago
- Pipeline code for creating a fully haplotype-resolved assembly from a combination of PacBio/ONT long reads and Illumina Strand-seq data☆16Apr 2, 2024Updated last year
- A visualization tool to support reviewing the scientific literature☆14Jun 2, 2018Updated 7 years ago
- A message queue for genomic surveillance☆20Oct 14, 2021Updated 4 years ago
- A collection of CSV/TSV Utilities☆13Jun 2, 2020Updated 5 years ago