superbobry / snpyLinks
A wrapper-library for reading openSNP data
☆49Updated 7 years ago
Alternatives and similar repositories for snpy
Users that are interested in snpy are comparing it to the libraries listed below
Sorting:
- Efficient handling of FASTQ files from Python☆51Updated last month
- Quality control methods for human genomic variants.☆62Updated 3 years ago
- Flexible Integration of Data with Deep LEarning☆50Updated 2 years ago
- High throughput, pain-free big data pipelines.☆30Updated 8 years ago
- Prediction of the 3D structure of the genome through statistically significant Hi-C contacts.☆21Updated 7 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 3 years ago
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- Recipes for bioinformatics analyses with scikit-bio☆42Updated 9 years ago
- Library for manipulating genomic variants and predicting their effects☆85Updated last year
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆71Updated 2 years ago
- Simple and efficient access to genomic data for deep learning models.☆42Updated 5 years ago
- Finding a scalable alternative to the VCF File for genomics analysis☆14Updated 8 years ago
- Vector space representation of genetic data☆36Updated 8 years ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- Examples for the Google Genomics Pipelines API.☆50Updated 7 years ago
- Yet Another Motif Discovery Algorithm☆53Updated 6 years ago
- VariantToolChest (VTC) is intended to be a powerful tool chest to analyze VCF files. I encourage anyone to contribute their tools and hel…☆25Updated 9 years ago
- Distributed execution of bioinformatics tools on Apache Spark. Apache 2 licensed.☆41Updated 6 months ago
- SevenBridges Python Api bindings☆46Updated 6 months ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆97Updated 2 years ago
- Reproducible machine learning analysis of gene expression and alternative splicing data☆126Updated 2 years ago
- A library for next generation genomics in Python 3☆18Updated 7 years ago
- Benchmarking toolkit for variant calling☆48Updated 4 years ago
- Population Stratification Analysis on Genomics Data Using Deep Learning☆26Updated 8 years ago
- ☆11Updated 8 years ago
- MyVariant.info: A BioThings API for human variant annotations☆95Updated last month
- Server wrapper that turns command line tools into web services☆60Updated 7 years ago
- A tool for running bioinformatics workflows locally or in the cloud.☆30Updated 5 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 12 years ago