convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
-
Updated
Sep 16, 2019 - Go
#
dbsnp
Here are 10 public repositories matching this topic...
Methods for mapping genomic data onto 3D protein structure.
binder
genomics
protein-data-bank
protein-structure
pyspark
mutations
dbsnp
protein-protein-interaction
protein-ligand-interactions
cyverse
protein-drug-interactions
mmtf-pyspark
-
Updated
May 17, 2022 - Jupyter Notebook
An Open Source Web Application for Genetic Data (SNPs) Data Crawling
snps
genome
genetic-algorithm
dbsnp
phenotype
snpedia
clinvar
omni
23andme
genetic-data
ancestrydna
data-crawling
rsid
genetic-tests
os-genome
-
Updated
Dec 8, 2022 - JavaScript
Warehousing DbSNP's JSON Data into PostgreSQL
-
Updated
Jun 26, 2018 - Python
Identification of cancer-causing variants
bioinformatics
annotations
clinical
dbsnp
variants
cancer-genomics
clinvar
diseases
cancer-research
grch37
cancer-detection
allele-frequencies
conservation-scores
functional-prediction
pathogenic-variants
dbnsfp
gnomad
clinical-significance
hereditary-cancer-syndrome
acmg-guidelines
-
Updated
Apr 19, 2024 - Python
biopython + VCF support, based on pyVCF
-
Updated
Jul 6, 2017 - Python
ETL scripts to populate caBIO database
python
java
database
perl
dbsnp
shell-scripts
pathways
transcriptomics
uniprotkb
unigene
etl-pipeline
-
Updated
Oct 19, 2021
Non-biallelic SNPs for population genetics and forensics.
-
Updated
Mar 18, 2018 - C
Improve this page
Add a description, image, and links to the dbsnp topic page so that developers can more easily learn about it.
Add this topic to your repo
To associate your repository with the dbsnp topic, visit your repo's landing page and select "manage topics."