arvkevi / ezancestryLinks
Easy genetic ancestry predictions in Python
☆65Updated 3 weeks ago
Alternatives and similar repositories for ezancestry
Users that are interested in ezancestry are comparing it to the libraries listed below
Sorting:
- Python-based preprocessing software for Illumina methylation arrays☆37Updated last year
- Peax is a tool for interactive visual pattern search and exploration in epigenomic data based on unsupervised representation learning wit…☆68Updated 2 years ago
- tools for reading, writing, merging, and remapping SNPs☆109Updated 3 months ago
- PRSKB is a website and command-line interface tool for calculating polygenic risk scores using GWA studies from the NHGRI-EBI Catalog.☆29Updated 10 months ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 4 years ago
- Interactive multi-omics data explorer to integrate and interactively explore transcripts, proteins and metabolites data.☆13Updated 2 months ago
- Scripts for miscelleneous bioinformatics tasks☆48Updated 5 years ago
- Universal RObust Peak Annotator☆16Updated last year
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆59Updated last week
- Get your science on a leash!☆29Updated last week
- Hail helper functions for the gnomAD project and Translational Genomics Group☆96Updated this week
- Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.☆115Updated last month
- Python Programming for Biologists☆135Updated 2 months ago
- ClinVar aggregates information about genomic variation and its relationship to human health. Contact us at 'clinvar@ncbi.nlm.nih.gov…☆81Updated 7 months ago
- ☆28Updated 3 months ago
- A declarative interactive genomics visualization library for Python.☆228Updated this week
- List of computational resources for analyzing microbial sequencing data.☆68Updated last month
- A cookiecutter template for Snakemake workflows☆59Updated 3 years ago
- Notebooks accompanying the paper "Navigating the pitfalls of applying machine learning in genomics"☆45Updated last year
- The GenePattern Server web application☆36Updated 2 months ago
- Platform for integrating genomic analysis with Jupyter Notebooks.☆44Updated 11 months ago
- Python bindings to and Jupyter Notebook+Lab integration for the HiGlass viewer☆59Updated 2 months ago
- Genome-wide imputation pipeline☆32Updated 11 months ago
- Efficient handling of FASTQ files from Python☆51Updated last month
- Monitor computational workflows in real time☆74Updated last year
- dbSNP☆137Updated last year
- ☆62Updated 8 years ago
- Germline Variant Calling Nextflow Pipeline Based On GATK4 Best Practices☆12Updated 5 years ago
- MyGene.info: A BioThings API for gene annotations☆127Updated last month
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆58Updated 5 years ago