#
genetics
Here are 630 public repositories matching this topic...
threejs
genetics
genetic-algorithm
evolutionary-algorithms
self-driving-car
cannonjs
three-js
evolutionary-algorithm
cannon-js
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Updated
Oct 13, 2021 - TypeScript
A comprehensive tutorial about GWAS and PRS
unix
bioinformatics
gwas
r
genomics
genetics
plink
prs
population-structure
qc
population-stratification
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Updated
Jan 3, 2020
A powerful open source data warehouse system
python
java
api
open-source
clojure
opensource
bioinformatics
genomics
genetics
clojurescript
biology
perl
postgresql
lgplv3
tomcat
data-visualization
data-warehouse
data-visualisation
webservices
tomcat8
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Updated
May 18, 2022 - Java
CellRank for directed single-cell fate mapping
data-science
machine-learning
bioinformatics
genetics
trajectory-generation
markov-chains
manifold-learning
single-cell-genomics
single-cell-rna-seq
cell-fate-transitions
fuzzy-clustering-analyses
rna-velocity
cell-fate-determination
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May 18, 2022 - Python
Simulate genealogical trees and genomic sequence data using population genetic models
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May 19, 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
c-plus-plus
gwas
kernel
genetics
ngs
next-generation-sequencing
variants
meta-analysis
genotype
umich
skat
association-analysis
rare-variant
vcf-files
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Updated
Jan 26, 2022 - C++
tools for genetic genealogy and the analysis of consumer DNA test results
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Updated
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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May 18, 2022 - Java
good first issue
Good for newcomers
help wanted
Extra attention is needed
core operations
Issues related to domain-specific functionality such as LD pruning, PCA, association testing, etc.
Streamlining phylogenomic data gathering, processing and visualization
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Updated
Sep 26, 2018 - Python
Resource of human chromosome schematics & images
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Updated
Dec 17, 2020
A curated list of awesome bioinformatics software.
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Updated
May 13, 2022
dridk
commented
May 12, 2022
@SamuelNicaise
Peux tu me faire des tests pour SampleDialog et VariantDialog dans tests/gui/widgets ?
Je viens d'en mettre , tu peux t'inspirer.
python -m pytests tests/gui/widgets
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
visualization
genomics
genetics
filter
outliers
imputation
missingness
gbs
normalization
radseq
radseq-data
genomic-data-analysis
genotype-likelihoods
genomics-visualization
genotyping-by-sequencing
batch-effects
heterozygosity
artifacts-detection
paralogs
outliers-detection
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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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Updated
Jan 21, 2020 - Python
Micutio
commented
Dec 9, 2020
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.
good first issue
Good for newcomers
Fast calculations of linkage-disequilibrium in large-scale human cohorts
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Updated
Nov 9, 2019 - C++
visualization
data-science
bioinformatics
gwas
genomics
genetics
julia
julia-language
qtl
linkage
phewas
colocalization
locuszoom
fine-mapping
makie
v2f
cairomakie
multi-ethnic
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Updated
May 7, 2022 - Julia
Framework for Interpretable Neural Networks
machine-learning
deep-learning
neural-network
genetics
neural-networks
genotype
interpretable-neural-networks
gennet
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Updated
May 19, 2022 - Jupyter Notebook
Digital Expression Explorer 2 (DEE2): a repository of uniformly processed RNA-seq data
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Updated
Apr 14, 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