Alternatives and similar repositories for gwas-pw-paper

Users that are interested in gwas-pw-paper are comparing it to the libraries listed below

• raymondkiu / R-scripts-graphing-statistics
  My R scripts, primarily R plotting scripts + some genomics software including 16S rRNA metataxnomics and RNAseq
  ☆12Updated 2 years ago
• mahajrod / MAVR
  various bioinformatic instruments
  ☆8Updated 5 months ago
• genomic-medicine-sweden / tomte
  A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient
  ☆14Updated last week
• datarail / rnaseq
  Deprecated, see https://labsyspharm.github.io/rnaseq/
  ☆12Updated 6 years ago
• pachterlab / kallisto-sleuth-workshop-2016
  materials and website for the 2016 kallisto sleuth workshop
  ☆11Updated 8 years ago
• NovembreLab / eems-around-the-world
  Repo to analyze population genetic data with many different methods
  ☆15Updated 5 years ago
• MorrellLAB / sequence_handling
  A series of scripts to automate sequence workflows
  ☆19Updated last month
• ipdgc / Manhattan-Plotter
  This is a repository to help make plots similar to Figure 2 in https://www.biorxiv.org/content/10.1101/388165v3
  ☆12Updated 6 years ago
• smped / ngsReports
  ☆22Updated 3 weeks ago
• artempronozin95 / ICAnnoLncRNA-identification-classification-and-annotation-of-LncRNA
  ☆9Updated 7 months ago
• mturchin20 / bmass
  R package for 'Bayesian multivariate analysis of summary statistics' (Stephens Lab)
  ☆10Updated 4 years ago
• oeco28 / Cacao_Genomics
  This is a basic repository with all the scripts necessary to reconstruct the data analysis from our work on the 200 Genomes
  ☆11Updated 6 years ago
• databio / bedshift
  Bedfile perturbation tool
  ☆17Updated last year
• CBC-UCONN / Structural-Annotation
  ☆12Updated 2 years ago
• bio-ontology-research-group / DeepSVP
  Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity
  ☆16Updated 3 years ago
• Zilong-Li / vcfppR
  The fastest VCF/BCF parser in R https://doi.org/10.1093/bioinformatics/btae049
  ☆15Updated 2 weeks ago
• VCCRI / dv-trio
  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
• nellore / runs
  Scripts for reproducing analyses of large RNA-seq datasets
  ☆15Updated 6 years ago
• wl13 / BioScripts
  Scripts for bioinformatics data processing and analysis
  ☆12Updated last year
• mcveanlab / TreeWAS
  ☆16Updated 7 years ago
• weissmanlab / magic
  Minimal Assumption Genomic Inference of Coalescence
  ☆14Updated last year
• hakha-most / gwas_eqtl
  ☆16Updated last year
• sunnyeesl / BigLD
  ☆21Updated 3 years ago
• pandora414 / lncRNA
  lncRNA分析流程
  ☆8Updated 6 years ago
• sestaton / sesbio
  Bioinformatics scripts for genome analysis
  ☆17Updated 2 years ago
• dyerlab / applied_population_genetics
  A textbook on population genetics
  ☆18Updated 7 months ago
• mdozmorov / RNA-seq
  RNA-seq analysis scripts
  ☆15Updated 2 months ago
• Baldridge37 / RNAseq_with_Hisat2_stringtie
  RNAseq analysis with Hisat2, stringtie, and ballgown
  ☆16Updated 5 years ago
• dongwei1220 / R-Data-Visualization
  Data visualization with R
  ☆12Updated 4 years ago
• filippob / introduction_to_gwas
  https://filippob.github.io/introduction_to_gwas/
  ☆20Updated 2 weeks ago