timyers / r-learning-resources-for-genomics

Related projects ⓘ

Alternatives and complementary repositories for r-learning-resources-for-genomics

• bioinformatics-core-shared-training / Bulk_RNAseq_Course_Base
  ☆13Updated last month
• jokergoo / KeywordsEnrichment
  ☆31Updated 10 months ago
• chunjie-sam-liu / useful-scripts
  common useful script
  ☆32Updated last week
• tobiasrausch / vc
  A tutorial on structural variant calling for short read sequencing data
  ☆26Updated 3 weeks ago
• Bioconductor / Rsamtools
  Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import
  ☆27Updated 3 weeks ago
• schatzlab / scikit-ribo
  Accurate estimation and robust modelling of translation dynamics at codon resolution
  ☆18Updated 7 years ago
• sk-sahu / sig-bio-shiny
  A standalone interactive application for detecting biological significance on a set of genes
  ☆40Updated 3 years ago
• js2264 / tidyCoverage
  ☆20Updated 2 months ago
• knausb / vcfR_documentation
  Documentation for vcfR
  ☆10Updated last year
• YinLiLin / SumTool
  Tool for GWAS summary-level data analysis
  ☆26Updated 4 years ago
• abodein / timeOmics
  Time-Course Multi-Omics data integration
  ☆24Updated 7 months ago
• NBISweden / workshop-mlbiostatistics
  ☆15Updated last month
• tobiasrausch / nRex
  nRex: Germline and somatic single-nucleotide, short indel and structural variant calling
  ☆12Updated last month
• guokai8 / bioAnno
  Build Annotation package by using information from KEGG, NCBI, Ensembl
  ☆15Updated last year
• atgu / GWASpy
  GWAS QC, PCA, haplotype phasing, genotype imputation
  ☆17Updated last month
• stevekm / Bioinformatics
  Bioinformatics analysis scripts, workflows, general code examples
  ☆53Updated 3 years ago
• kevinblighe / ClinicalGradeDNAseq
  Automated next generation DNA sequencing analysis pipeline suited for clinical tests, with >99.9% sensitivity to Sanger sequencing at rea…
  ☆25Updated 4 years ago
• crazyhottommy / scripts-general-use
  ☆16Updated 7 years ago
• crazyhottommy / pyflow-RNAseq
  RNAseq pipeline based on snakemake
  ☆22Updated last year
• OSU-BMBL / IRIS
  A Shiny web server for interactive visualization and analysis of RNA-seq data
  ☆22Updated 3 years ago
• mkanai / grimon
  R package for plotting 3D graphical visualization of multi-omics data.
  ☆22Updated 2 years ago
• neurogenomics / orthogene
  🧬 o r t h o g e n e 🧬✨✨✨✨✨✨✨ Interspecies gene mapping✨✨✨✨✨ 🦠 🔁 🌱 🔁 🌳 🔁 🍎 🔁 🍊 🔁 🪱 🔁 🪰 🔁 🐟 🔁 🦎 🔁 🐓 🔁 🦇 🔁 🐄 🔁 �…
  ☆40Updated 10 months ago
• crazyhottommy / oneliner_100day_challenge
  Bioinformatics one-liner for 100 days
  ☆43Updated 7 months ago
• 123xiaochen / VCFshiny
  ☆26Updated last month
• NBISweden / workshop-ngsintro
  Workshop • Intro to Bioinformatics using NGS data • 5 days
  ☆13Updated this week
• ctb / 2019-snakemake-ucdavis
  Intro to workflows for efficient automated data analysis, using snakemake.
  ☆32Updated 5 years ago
• cxli233 / ggtraces
  A tidyverse and grammar of graphics powered line traces visualizer
  ☆26Updated 4 months ago
• PawseySC / bio-workshop-18
  Pawsey workshop: containers for bioinformatics
  ☆19Updated 5 years ago
• NBISweden / GUESSmyLT
  An efficient way to guess the library type of your RNA-Seq data.
  ☆29Updated 2 years ago
• n-mounier / bGWAS
  R package to perform Bayesian Genome-Wide Association Studies
  ☆38Updated last year
• YuLab-SMU / MicrobiomeProfiler
  A shiny package for microbiome functional enrichment analysis
  ☆36Updated 3 weeks ago