swarris / pyPaSWASLinks
Program for DNA/RNA/protein sequence alignment, read mapping and trimming. Extended python version of PaSWAS, supporting OpenCL and CUDA devices.
☆28Updated 2 years ago
Alternatives and similar repositories for pyPaSWAS
Users that are interested in pyPaSWAS are comparing it to the libraries listed below
Sorting:
- Genetics training camp☆21Updated 4 years ago
- MerCat: python code for versatile k-mer counting and diversity estimation for database independent property analysis for meta -ome data☆18Updated 2 years ago
- Deep Feature Interaction Maps (DFIM)☆53Updated 6 years ago
- Concise: Keras extension for regulatory genomics☆35Updated 2 years ago
- Fishers Exact Test for Python (Cython)☆66Updated 4 months ago
- A repository for the GenGraph toolkit for the creation and manipulation of graph genomes☆51Updated 3 years ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- Simple and efficient access to genomic data for deep learning models.☆43Updated 5 years ago
- A Python library for reading and writing PacBio® data files☆39Updated 5 months ago
- CNN based classifier for detecting viral sequences among metagenomic contigs☆33Updated 4 years ago
- Flexible Integration of Data with Deep LEarning☆50Updated 2 years ago
- ☆79Updated last month
- A unified array job submitter for LSF, SGE/UGE and Slurm☆32Updated 9 months ago
- Haplotype, isoform and gene level expression analysis using multi-mapping RNA-seq reads☆68Updated last year
- Library for manipulating genomic variants and predicting their effects☆84Updated last year
- FFPopSim is a collection of C++ classes and a Python interface for efficient simulation of large populations, in particular when the prod…☆14Updated 2 months ago
- Efficient handling of FASTQ files from Python☆51Updated 2 months ago
- A software for the multispecies design of CRISPR/Cas9 libraries☆36Updated 2 years ago
- Code for the CRISPOR article, all data and code to create figures and analysis☆40Updated 8 years ago
- This repository contains Jupyter Notebooks containing GATK Best Practices Workflows☆26Updated 5 years ago
- sequence alignment. global, local, glocal.☆41Updated 8 years ago
- Single-Cell RNA-seq pseudo-aligner☆51Updated last year
- a python package for KEGG pathway enrichment analysis with multiple gene lists.☆36Updated 7 years ago
- Boiler: a software tool for highly efficient, lossy compression of RNA-seq alignments☆13Updated 9 years ago
- Downloader for ENCODE☆32Updated 4 years ago
- Scripts related to building major-allele references for Bowtie and Bowtie 2☆13Updated 4 years ago
- Arioc: GPU-accelerated DNA short-read alignment☆70Updated 2 months ago
- Python package to analyze DNA methylation data☆43Updated 8 months ago
- Computational pipeline for calling consensi on R2C2 nanopore data☆31Updated 3 years ago
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated last year