superbobry / snpy
A wrapper-library for reading openSNP data
☆50Updated 6 years ago
Alternatives and similar repositories for snpy:
Users that are interested in snpy are comparing it to the libraries listed below
- Quality control methods for human genomic variants.☆62Updated 2 years ago
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆69Updated last year
- Biological Graphic tool in Python☆34Updated 4 years ago
- Efficient handling of FASTQ files from Python☆51Updated 5 months ago
- Simple and efficient access to genomic data for deep learning models.☆43Updated 5 years ago
- Flexible Integration of Data with Deep LEarning☆50Updated last year
- High throughput, pain-free big data pipelines.☆30Updated 7 years ago
- Library for manipulating genomic variants and predicting their effects☆83Updated 7 months ago
- This is a short response to the 2018 RFI on NIH Strategic Plan for Data Science☆16Updated 6 years ago
- A software for the multispecies design of CRISPR/Cas9 libraries☆34Updated 2 years ago
- Prediction of the 3D structure of the genome through statistically significant Hi-C contacts.☆21Updated 6 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- DSDE Deep Learning Club☆40Updated 5 years ago
- [DEPRECATED] An R package for Google Genomics API queries.☆45Updated last year
- Python client for MyVariant.info web services.☆22Updated last month
- Python library and scripts for retrieval and storage of genomics data in HDF5 format☆26Updated 5 years ago
- A collection of well-known bioinformatics programs.☆25Updated 9 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- [Historical] Reproducible Analyses for Bioinformatics☆106Updated 5 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 11 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 2 years ago
- Deep Feature Interaction Maps (DFIM)☆53Updated 5 years ago
- Computational biology utility scripts☆19Updated 7 months ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 6 years ago
- Genevieve genome report tool☆14Updated 2 years ago
- Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆30Updated 7 years ago
- Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data☆87Updated 4 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- An open-source high-performance web-based HTML5 genome browser. Genome Maps can be customized and allow browsing user data such as BAM an…☆38Updated 6 years ago
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆73Updated 3 weeks ago