Alternatives and similar repositories for Genome-Analysis-Tutorial:

Users that are interested in Genome-Analysis-Tutorial are comparing it to the libraries listed below

• JunKim-Worms / sequencing_for_genetics
  유전학자를 위한 시퀀싱 자료 분석
  ☆23Updated 4 years ago
• crazyhottommy / scripts-general-use
  ☆16Updated 7 years ago
• bioinformatics-ca / bioinformatics-ca.github.io
  Student website repo for 2015/2016 Canadian Bioinformatics Workshops
  ☆34Updated last year
• dvitsios / mirnovo
  Genome free discovery and classification of miRNAs from small RNA-Seq with random forests
  ☆11Updated 6 years ago
• gagneurlab / FRASER
  FRASER - Find RAre Splicing Events in RNA-seq
  ☆44Updated 3 weeks ago
• schatzlab / appliedgenomics2018
  Materials for Spring 2018 Applied Genomics Course
  ☆78Updated 6 years ago
• bioinformaticsdotca / bioinformaticsdotca.github.io
  Repo for student website
  ☆24Updated last month
• sk-sahu / sig-bio-shiny
  A standalone interactive application for detecting biological significance on a set of genes
  ☆40Updated 3 years ago
• melbournebioinformatics / variant_calling_pipeline
  A simple variant calling and annotation pipeline using BWA, GATK and ENSEMBL. This version of the pipeline uses the Rubra/Ruffus framewor…
  ☆34Updated 11 years ago
• stevekm / Bioinformatics
  Bioinformatics analysis scripts, workflows, general code examples
  ☆53Updated 4 years ago
• rkitchen / exceRpt
  Software for preprocessing, filtering, alignment, and reporting of smallRNA-seq datasets
  ☆19Updated 4 years ago
• hamidghaedi / Enrichment-Analysis
  From RNA-seq raw reads to enriched pathways by DEGs
  ☆33Updated 11 months ago
• hyeshik / poreplex
  A versatile sequenced read processor for nanopore direct RNA sequencing
  ☆79Updated 4 years ago
• bharani-lab / WES-Benchmarking-Pipeline_Manoj
  Benchmarking of aligners and variant callers for Whole Exome Sequencing data
  ☆19Updated 6 years ago
• sheynkman-lab / Long-Read-Proteogenomics
  A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
  ☆45Updated 2 years ago
• nf-core / dualrnaseq
  Analysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.
  ☆21Updated this week
• parklab / LiRA
  ☆18Updated 3 years ago
• nf-core / rnavar
  gatk4 RNA variant calling pipeline
  ☆45Updated last week
• crazyhottommy / compbio_resources_chatomics
  ☆27Updated last year
• drtamermansour / nu-ngs01
  NGS-1 Data analysis course
  ☆36Updated 3 years ago
• crazyhottommy / pyflow-RNAseq
  RNAseq pipeline based on snakemake
  ☆25Updated 2 years ago
• biocore / tcga
  Microbial analysis in TCGA data
  ☆90Updated last year
• cancerit / BRASS
  Breakpoints via assembly - Identifies breaks and attempts to assemble rearrangements in whole genome sequencing data.
  ☆57Updated 8 months ago
• davetang / learning_vcf_file
  Learning the Variant Call Format
  ☆139Updated last year
• microbiome / mia
  Microbiome analysis
  ☆51Updated this week
• griffithlab / rnaseq_tutorial_wiki
  The wiki repo, with pull request enabled, for the rnaseq_tutorial
  ☆26Updated 4 years ago
• biostars / biostar-handbook
  Issue tracker for the Biostar Handbook
  ☆62Updated 2 years ago
• drpowell / degust
  An interactive web-tool for RNA-seq analysis
  ☆68Updated last month
• raynamharris / Shell_Intro_for_Bioinformatics_STG
  Intro to Shell for Bioinformatics - with STG examples
  ☆28Updated 8 years ago
• LabTranslationalArchitectomics / riboWaltz
  optimization of ribosome P-site positioning in ribosome profiling data
  ☆50Updated last month