convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
☆100Aug 27, 2019Updated 6 years ago
Alternatives and similar repositories for 23andme2vcf
Users that are interested in 23andme2vcf are comparing it to the libraries listed below
Sorting:
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆60Sep 16, 2019Updated 6 years ago
- Source code for ScanGEO Shiny App☆15Apr 18, 2022Updated 3 years ago
- A genotype query interface.☆136Mar 29, 2021Updated 4 years ago
- Flexible genotype query among 30,000+ samples whole-genome☆94Sep 4, 2019Updated 6 years ago
- Tools to work with 23andMe and AncestryDNA raw files☆12Aug 5, 2017Updated 8 years ago
- Genealogy Tools☆14Jan 7, 2021Updated 5 years ago
- Normalization and difference calling for Next Generation Sequencing (NGS) data via joint multinomial modeling.☆11Oct 8, 2021Updated 4 years ago
- zero-inflated negative binomial gene expression in R☆20Jan 31, 2018Updated 8 years ago
- High-performance error correction for Illumina resequencing data☆74May 31, 2016Updated 9 years ago
- Genetic visualization application using Python/Flask, Angular, d3, and 23andMe authentication☆14Aug 5, 2016Updated 9 years ago
- Easy access to human reference genome sequences☆58Apr 6, 2023Updated 2 years ago
- Examples for the Google Genomics Pipelines API.☆50Dec 15, 2017Updated 8 years ago
- User-friendly Bioinformatics Tools☆18Mar 5, 2021Updated 5 years ago
- A flexible framework for rapid genome analysis and interpretation☆319Oct 18, 2022Updated 3 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- SVsim: a tool that generates synthetic Structural Variant calls as benchmarks to test/evaluate SV calling pipelines.☆18Dec 4, 2017Updated 8 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Feb 7, 2017Updated 9 years ago
- annotate a VCF with other VCFs/BEDs/tabixed files☆398Aug 30, 2025Updated 6 months ago
- Estimate linkage disequilibrium between unphased loci☆11Jun 9, 2015Updated 10 years ago
- method to estimate PCR duplication rate from high-throughput sequencing data☆15Sep 22, 2017Updated 8 years ago
- ALOFT, the Annotation Of Loss-of-Function Transcripts, provides extensive functional annotations to loss-of-function variants in the hum…☆19Nov 4, 2019Updated 6 years ago
- Collection of notes and scripts related to NGS☆14Feb 18, 2026Updated last month
- laSV is a software package that employs local assembly to detect structural variations from whole-genome high-throughput sequencing datas…☆12Sep 26, 2016Updated 9 years ago
- Identify cell types and pathways affected by genetic risk loci.☆36Feb 29, 2024Updated 2 years ago
- A fast 23andMe DNA parser and inferrer for Python☆123Nov 9, 2019Updated 6 years ago
- Analyse a genome file from 23andMe using the data on snpedia.com☆21Feb 7, 2017Updated 9 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Jun 4, 2024Updated last year
- SVG based genome viewer written in javascript using D3☆33Jul 12, 2015Updated 10 years ago
- Parallel Block GZIP☆50Aug 4, 2016Updated 9 years ago
- A GA4GH Draft Beacon implementation☆11Oct 23, 2015Updated 10 years ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆123Feb 6, 2026Updated last month
- A tool to examine duplicate read characteristics in a BAM file☆12Dec 8, 2017Updated 8 years ago
- Shape analysis of high-throughput data☆19Feb 24, 2016Updated 10 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11May 2, 2017Updated 8 years ago
- an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.☆73Aug 22, 2022Updated 3 years ago
- A tool set for short variant discovery in genetic sequence data.☆204May 4, 2021Updated 4 years ago
- A shell script which implements GATK pipeline for variant calling.☆15Nov 30, 2014Updated 11 years ago
- R function to plot high quality, elegant heatmap using 'ggplot2' graphics . Some of the important features of this package are, colorin…☆11Apr 19, 2016Updated 9 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Jul 10, 2017Updated 8 years ago