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probalign
|
public |
Probalign: multiple sequence alignment using partition function posterior probabilities
|
2025-03-25 |
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opal
|
public |
Opal is software for aligning multiple biological sequences.
|
2025-03-25 |
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contralign
|
public |
CONditional TRAining for Biosequence Analysis
|
2025-03-25 |
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rb-mustache
|
public |
framework-agnostic way to render logic-free views
|
2025-03-25 |
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ronn
|
public |
Builds manuals - the opposite of roff
|
2025-03-25 |
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rb-rdiscount
|
public |
Fast Implementation of Gruber's Markdown in C
|
2025-03-25 |
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rb-hpricot
|
public |
a swift, liberal HTML parser with a fantastic library
|
2025-03-25 |
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r-qrank
|
public |
A Quantile Rank-score based test for the identification of expression quantitative trait loci.
|
2025-03-25 |
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ldetect
|
public |
Package for detecting regions of linkage disequilibrium in the human genome
|
2025-03-25 |
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pup
|
public |
Parsing HTML at the command line
|
2025-03-25 |
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libsixel
|
public |
SIXEL encoder/decoder implementation
|
2025-03-25 |
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jq-lsp
|
public |
jq language server
|
2025-03-25 |
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groovy-language-server
|
public |
A language server for Groovy
|
2025-03-25 |
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git-fixup
|
public |
Fighting the copy-paste element of your rebase workflow.
|
2025-03-25 |
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colortail
|
public |
Like the tail command line utility but with colors
|
2025-03-25 |
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sda
|
public |
A program for sparse Bayesian matrix and tensor decomposition.
|
2025-03-25 |
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impute5
|
public |
IMPUTE 5 is a genotype imputation method that can scale to reference panels with millions of samples.
|
2025-03-25 |
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snptest
|
public |
SNPTEST is a program for the analysis of single SNP association in genome-wide studies.
|
2025-03-25 |
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meta
|
public |
META is a program for the meta analysis of genome-wide association studies.
|
2025-03-25 |
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gtool
|
public |
GTOOL is a program for transforming sets of genotype data for use with the programs SNPTEST and IMPUTE.
|
2025-03-25 |
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vipcca
|
public |
No Summary
|
2025-03-25 |
|
r-pqlseq
|
public |
An efficient tool designed for differential analysis of large-scale RNA sequencing (RNAseq) data and Bisulfite sequencing (BSseq) data in the presence of individual relatedness and population structure. 'PQLseq' first fits a Generalized Linear Mixed Model (GLMM) with adjusted covariates, predictor of interest and random effects to account for population structure and individual relatedness, and then performs Wald tests for each gene in RNAseq or site in BSseq.
|
2025-03-25 |
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r-viper
|
public |
The package implements a straightforward, accurate, free-of-tuning, and relatively computationally efficient scRNAseq imputation method.
|
2025-03-25 |
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r-metro
|
public |
Multi-ancEstry TRanscriptOme-wide analysis
|
2025-03-25 |
|
r-mesusie
|
public |
Multi-ancestry Sum of the Single Effects Model
|
2025-03-25 |
