apierleoni / BioGraPyLinks
Biological Graphic tool in Python
☆34Updated 5 years ago
Alternatives and similar repositories for BioGraPy
Users that are interested in BioGraPy are comparing it to the libraries listed below
Sorting:
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 7 months ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 11 months ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆52Updated 7 years ago
- Malleable All-seeing Journal Of Research Artifacts☆36Updated 2 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- http://www.combio.pl/alfree☆23Updated 3 years ago
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated last year
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- python wrapper to dpryan79's bigwig library using cffi☆19Updated 9 years ago
- A flexible python program for generating figures from regions of the genome.☆13Updated 6 years ago
- ☆13Updated 7 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated 2 months ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆40Updated 4 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆51Updated 7 months ago
- Tools for next-generation sequencing analysis☆88Updated 6 years ago
- Reference-free variant discovery in large eukaryotic genomes☆41Updated 4 years ago
- Metagenomic profiling and phylogenetic distances via common kmers☆42Updated 4 years ago
- Exploration, clustering, visualization and classification of DNA damage patterns☆19Updated 4 years ago
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆23Updated 4 years ago
- Master of Pores 2☆23Updated 7 months ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- 🍶 Genome assembly with short sequence reads☆25Updated last year
- Code to reproduce analyses from the sleuth paper☆16Updated 6 years ago
- Demonstrating best practices for bioinformatics command line tools☆26Updated 4 years ago
- simple library for dealing with SAM cigar strings☆41Updated 4 years ago