PickrellLab / gwas-pw-paperLinks
☆13Updated 9 years ago
Alternatives and similar repositories for gwas-pw-paper
Users that are interested in gwas-pw-paper are comparing it to the libraries listed below
Sorting:
- materials and website for the 2016 kallisto sleuth workshop☆11Updated 9 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- My R scripts, primarily R plotting scripts + some genomics software including 16S rRNA metataxnomics and RNAseq☆12Updated 3 years ago
- Deprecated, see https://labsyspharm.github.io/rnaseq/☆12Updated 6 years ago
- ggplot2-based Manhattan plot☆12Updated 3 years ago
- Scripts for bioinformatics data processing and analysis☆12Updated 2 years ago
- ☆23Updated last month
- An R package to detect, classify, and visualize genome rearrangements☆15Updated 5 years ago
- A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient☆18Updated last month
- GenomeTools: Scripts and Classes for Working with Genomic Data☆12Updated 7 years ago
- ☆18Updated 2 years ago
- R package for 'Bayesian multivariate analysis of summary statistics' (Stephens Lab)☆10Updated 5 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Updated 4 years ago
- ☆10Updated 6 years ago
- This is a repository to help make plots similar to Figure 2 in https://www.biorxiv.org/content/10.1101/388165v3☆13Updated 6 years ago
- RNAseq analysis with Hisat2, stringtie, and ballgown☆17Updated 6 years ago
- A series of scripts to automate sequence workflows☆19Updated 7 months ago
- ☆16Updated 8 years ago
- GWAS and rare variants tests at high speed using regenie☆16Updated 2 months ago
- R Interface to the NCBI SRA metadata☆23Updated 7 years ago
- Machine learning use cases for teaching☆13Updated 8 years ago
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆16Updated 3 years ago
- Code used to process and analyze structural variants and short tandem repeat variants profiled in 719 deeply sequenced whole genomes as p…☆11Updated 6 years ago
- Tao Yan's Plot Toolkit☆12Updated 6 years ago
- mitochondrial variant analysis tools☆15Updated 4 years ago
- TOP results by CONfident efFECT Sizes.☆15Updated last year
- Data visualization with R☆12Updated 5 years ago
- RNA-seq analysis scripts☆15Updated last month
- CLI to automate Nextflow pipeline testing☆12Updated 2 weeks ago
- Bedfile perturbation tool☆17Updated 3 months ago