libnano / primer3-pyLinks
Simple oligo analysis and primer design
☆187Updated last week
Alternatives and similar repositories for primer3-py
Users that are interested in primer3-py are comparing it to the libraries listed below
Sorting:
- a python package for fast random access to sequences from plain and gzipped FASTA/Q files☆289Updated this week
- Primer3 is a command line tool to select primers for polymerase chain reaction (PCR).☆272Updated 8 months ago
- GFF and GTF file manipulation and interconversion☆312Updated last year
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆128Updated 5 years ago
- Extension for Jupyter which integrates igv.js☆154Updated 3 years ago
- Package for fetching metadata and downloading data from SRA/ENA/GEO☆348Updated last month
- GFF and GVF specification documents☆219Updated last year
- Next generation sequencing reads de novo assembler.☆239Updated 4 months ago
- A fast Python and command-line utility for extracting simple statistics against genome positions based on sequence alignments from a SAM …☆195Updated 2 weeks ago
- Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.☆386Updated 7 months ago
- Read trimming tool for Illumina NGS data.☆150Updated 10 years ago
- Basecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files☆119Updated last month
- classify, merge, tracking and annotation of GFF files by comparing to a reference annotation GFF☆254Updated 6 months ago
- GFF/GTF utility providing format conversions, region filtering, FASTA sequence extraction and more☆451Updated last year
- PAired-eND Assembler for DNA sequences☆137Updated 5 years ago
- UCSC Genome Browser source. "beta" is released version / "master" is testing.☆250Updated this week
- Tools for manipulating biological data, particularly multiple sequence alignments☆159Updated last month
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆107Updated 7 months ago
- FASTA/FASTQ pre-processing programs☆195Updated 3 years ago
- Transcript discovery and quantification with long RNA reads (Nanopores and PacBio)☆199Updated this week
- breseq is a computational pipeline for finding mutations relative to a reference sequence using high-throughput DNA resequencing data. It…☆174Updated 2 months ago
- Windowed Adaptive Trimming for fastq files using quality☆226Updated 8 years ago
- V-pipe is a pipeline designed for analysing NGS data of short viral genomes☆144Updated 2 months ago
- ☆299Updated last month
- Sequana: a set of Snakemake NGS pipelines☆151Updated this week
- Align proteins to genomes with splicing and frameshift☆394Updated 2 weeks ago
- HiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.☆263Updated 6 months ago
- Genome browser and variant annotation☆387Updated 2 months ago
- PacBio Secondary Analysis Tools on Bioconda. Contains list of PacBio packages available via conda.☆285Updated 11 months ago
- SortMeRNA: next-generation sequence filtering and alignment tool☆282Updated 5 months ago