glasgowm148 / Phenotype
An Open Source Web Application for Genetic Data (SNPs) Data Crawling
☆18Updated 2 years ago
Alternatives and similar repositories for Phenotype:
Users that are interested in Phenotype are comparing it to the libraries listed below
- A curated list of awesome personal genomics software, libraries, and educational resources.☆134Updated last year
- DNA-Seq pipeline☆28Updated 4 months ago
- An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies☆129Updated last year
- dbSNP☆133Updated 10 months ago
- tools for reading, writing, merging, and remapping SNPs☆108Updated last month
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆56Updated 5 years ago
- Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`☆268Updated last week
- To preprocess, quality control and prepare consumer DTC genomes for research☆14Updated 2 weeks ago
- Fetches PubMed article IDs (PMIDs) from email inbox, then crawls PubMed, Google Scholar and Sci-Hub for respective PDF files.☆34Updated 6 years ago
- Analysis of deep sequencing data for rapid and intuitive interpretation of genome editing experiments☆297Updated 3 weeks ago
- WGS Extract Developers Repository☆24Updated last year
- Python package with helper tools for the nf-core community.☆256Updated last week
- Lollipop-style mutation diagrams for annotating genetic variations.☆189Updated 7 months ago
- Explore gnomAD datasets on the web☆84Updated last week
- Easy access to human reference genome sequences☆56Updated 2 years ago
- tools for genetic genealogy and the analysis of consumer DNA test results☆167Updated last month
- The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants☆476Updated 3 weeks ago
- TransVar - multiway annotator for precision medicine☆125Updated 2 years ago
- Easy genetic ancestry predictions in Python☆65Updated last month
- The next version of bwa-mem☆750Updated 8 months ago
- fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing☆739Updated 3 months ago
- genetic variant expressions, annotation, and filtering for great good.☆259Updated last month
- Embeddable genomic visualization component based on the Integrative Genomics Viewer☆671Updated this week
- Open source engine for matching cancer patients to precision medicine clinical trials (V2).☆36Updated last year
- A Curated List of Computational Biology Datasets Suitable for Machine Learning☆171Updated last year
- PDF Downloader with SCI-HUB☆48Updated last year
- List of gene lists for genomic analyses.☆219Updated 2 years ago
- web-based analysis tool for rare disease genomics☆187Updated last week
- Tools for working with genomic and high throughput sequencing data.☆325Updated this week
- Associations of genomic features, drugs and diseases☆48Updated 2 years ago