convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
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Updated
Sep 16, 2019 - Go
convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
Methods for mapping genomic data onto 3D protein structure.
An Open Source Web Application for Genetic Data (SNPs) Data Crawling
Warehousing DbSNP's JSON Data into PostgreSQL
Identification of cancer-causing variants
biopython + VCF support, based on pyVCF
Scripts that collect dbSNP, ClinVar and OMIM variants of the human insulin signaling and tryptophan metabolism pathway genes (2018)
ETL scripts to populate caBIO database
Local-first 23andMe and DTC DNA raw data to VCF 4.2 converter with PySide6 GUI, GRCh37/GRCh38 detection, and dbSNP/FASTA REF lookup
Curated, cited per-variant genomics notes (genetics + diet/lifestyle/region evidence) built from open APIs. DNA is the source of truth; region/diet are context.
Non-biallelic SNPs for population genetics and forensics.
This folder contains R scripts for differential expression analysis and analyses of tissue-specific expression, inter-species conservation, and genetic variations of the CAPN10 gene in a bioinformatics project on PCOS and insulin resistance.
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