glasgowm148 / PhenotypeLinks
An Open Source Web Application for Genetic Data (SNPs) Data Crawling
☆19Updated 2 years ago
Alternatives and similar repositories for Phenotype
Users that are interested in Phenotype are comparing it to the libraries listed below
Sorting:
- A curated list of awesome personal genomics software, libraries, and educational resources.☆138Updated last year
- An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies☆135Updated last year
- tools for genetic genealogy and the analysis of consumer DNA test results☆169Updated last month
- tools for reading, writing, merging, and remapping SNPs☆109Updated 5 months ago
- Fetches PubMed article IDs (PMIDs) from email inbox, then crawls PubMed, Google Scholar and Sci-Hub for respective PDF files.☆35Updated 6 years ago
- A fast 23andMe DNA parser and inferrer for Python☆121Updated 5 years ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆58Updated 5 years ago
- Genome-scale metabolic model of Methylococcus capsulatus.☆12Updated 6 years ago
- Easy genetic ancestry predictions in Python☆65Updated 2 months ago
- DNA-Seq pipeline☆28Updated 8 months ago
- NCBI Datasets is a new resource that lets you easily gather data from across NCBI databases.☆448Updated last week
- Genomics Extension for SQLite☆166Updated 11 months ago
- Quickly search, compare, and analyze genomic and metagenomic data sets.☆519Updated this week
- A box containing all necessary components to play with ultrasound.☆10Updated 4 years ago
- ☆23Updated 6 years ago
- Analyse a genome file from 23andMe using the data on snpedia.com☆21Updated 8 years ago
- Download books from a 📚 Goodreads shelf using ⛵ Library Genesis.☆88Updated 5 years ago
- PDF Downloader with SCI-HUB☆49Updated 2 years ago
- python Circos☆361Updated last year
- Python library to plot DNA sequence features (e.g. from Genbank files)☆649Updated 2 months ago
- To preprocess, quality control and prepare consumer DTC genomes for research☆14Updated 4 months ago
- Wetlab Calculator☆14Updated 8 months ago
- Schema and generated objects for biolink data model and upper ontology☆201Updated last week
- Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`☆273Updated last week
- ☆118Updated 2 months ago
- A curated list of resources for learning bioinformatics.☆488Updated 3 years ago
- A Tool to Annotate and Prioritize Exome Variants☆226Updated this week
- This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.gith…☆798Updated last week
- Code and data for GeneGPT.☆411Updated 3 months ago
- Ultra-deep search for novel viruses☆273Updated 2 years ago