nickFurlotte / pylmm
A fast and lightweight python-based linear mixed-model solver for use in genome-wide association studies.
☆43Updated 9 years ago
Alternatives and similar repositories for pylmm:
Users that are interested in pylmm are comparing it to the libraries listed below
- Functional genomics and genome-wide association studies☆67Updated 6 years ago
- A wrapper for liftOver for converting plink genotype data between different genome reference builds☆51Updated 6 years ago
- Accessing Intra-Tumor Heterogeneity and Tracking Longitudinal and Spatial Clonal Evolutionary History by Next-Generation Sequencing.☆68Updated 3 years ago
- Package to detect eQTLs jointly in multiple subgroups (e.g. tissues) via Bayesian Model Averaging.☆22Updated 7 years ago
- Get SNP proxies from the 1000 Genomes Project.☆28Updated 6 years ago
- Linear mixed model for genomic analyses.☆104Updated 3 years ago
- combining p-values using modified stouffer-liptak for spatially correlated results (probes)☆44Updated 3 years ago
- Sanity check Variant Call Format (VCF) files.☆37Updated 9 years ago
- Companion repo for ExAC paper, 2015☆33Updated 8 years ago
- ☆53Updated 2 months ago
- Exon-exon splice junctions across SRA☆40Updated 3 years ago
- An R package for import, QC and analysis of Illumina Infinium genotyping arrays☆34Updated 7 years ago
- Normalization for single cell RNA-seq data☆47Updated last year
- Report reverse and ambiguous strand SNPs in GWAS data☆32Updated 5 years ago
- Smooth quantile normalization (qsmooth) is a generalization of quantile normalization, which is an average of the two types of assumption…☆51Updated 2 years ago
- consistent quantification of external RNA-seq data sets☆58Updated last year
- Battenberg algorithm and associated implementation script☆52Updated 4 years ago
- Robust Allele Specific Quantification and quality controL☆39Updated 3 years ago
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆48Updated 5 years ago
- Generalized linear Mixed Model Association Tests☆41Updated last year
- ☆35Updated 8 years ago
- create, manage, and upload track hubs for use in the UCSC genome browser☆54Updated last year
- An archived version of the scater repository, see https://github.com/davismcc/scater for the active version.☆64Updated 7 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- ☆25Updated 11 months ago
- An R package for inferring the subclonal architecture of tumors☆117Updated last year
- Lightweight Iterative Gene set Enrichment in R☆56Updated 6 months ago
- ☆40Updated 7 years ago
- SPP - R package for analysis of ChIP-seq and other functional sequencing data☆42Updated 3 years ago
- A factor analysis package☆100Updated 12 years ago