genetics
Here are 622 public repositories matching this topic...
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Oct 13, 2021 - TypeScript
A comprehensive tutorial about GWAS and PRS
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Jan 3, 2020
A powerful open source data warehouse system
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Apr 8, 2022 - Java
CellRank for directed single-cell fate mapping
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Apr 7, 2022 - Python
Simulate genealogical trees and genomic sequence data using population genetic models
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Apr 4, 2022 - Python
Population-scale genotyping using pangenome graphs
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Feb 22, 2022 - C++
Rare variant test software for next generation sequencing data
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Jan 26, 2022 - C++
This is the code behind the www.impute.me site. It contains algorithms for personal genome analysis, including imputation and polygenic risk score calculation
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Jan 2, 2022 - R
tools for genetic genealogy and the analysis of consumer DNA test results
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Mar 12, 2022 - Python
Annotation and Ranking of Structural Variation
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Jan 25, 2022 - Tcl
MOLGENIS - for scientific data: management, exploration, integration and analysis.
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Apr 5, 2022 - Java
Streamlining phylogenomic data gathering, processing and visualization
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Sep 26, 2018 - Python
Resource of human chromosome schematics & images
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Dec 17, 2020
It looks strange to have the VQL autocompleter adding a space ..
It makes query like this :
SELECT chr ,pos , ....
Please remove the space insert after autocompletion .
A curated list of awesome bioinformatics software.
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Dec 10, 2017
VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
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Jan 25, 2022 - mupad
A minimal desktop app for easy and convenient gene annotation.
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Mar 25, 2022 - JavaScript
RADseq Data Exploration, Manipulation and Visualization using R
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Dec 22, 2021 - R
As a part of COVID-19 Host Genetics Initiative, we perform the following set of analyses to better understand the genetic basis of COVID-19 susceptibility and severity.
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May 7, 2020 - Jupyter Notebook
Create regional association plots from GWAS or meta-analysis
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Jan 21, 2020 - Python
Innit's unit tests currently only cover a small percentage of the codebase. Ideally at least all core functionalities e.g.: genetics, actions etc would be covered by automated tests.
Fast calculations of linkage-disequilibrium in large-scale human cohorts
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Nov 9, 2019 - C++
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Apr 8, 2022 - Julia
Digital Expression Explorer 2 (DEE2): a repository of uniformly processed RNA-seq data
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Apr 6, 2022 - Shell
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For association testing and PCA (at least), it may be useful to have a function that imputes dosages/allele counts. With floating point values (i.e. from bgen), this can be very simple as a user, e.g.
ds.call_genotype_probability.fillna(ds.call_genotype_probability.mean(dim="samples")). With alternate allele counts having a sentinel integer, it is a little more complicated. The best way t