Alternatives and similar repositories for Coursera_Bioinformatics_for_Beginners

Users that are interested in Coursera_Bioinformatics_for_Beginners are comparing it to the libraries listed below

• mdozmorov / RNA-seq
  RNA-seq analysis scripts
  ☆15Updated 2 weeks ago
• epigen / open_pipelines
  Pipelines for NGS data preprocessing by the Bock lab and friends
  ☆21Updated 2 years ago
• jiujiezz / tsnad
  Detecting somatic mutations and predicting tumor-specific neo-antigens
  ☆28Updated 3 years ago
• jsh58 / DMRfinder
  Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data
  ☆27Updated last year
• gencorefacility / r-notebooks
  Gene Set Enrichment Analysis and Over Representation Analysis analysis using R
  ☆20Updated 5 years ago
• NBISweden / workshop-mlbiostatistics
  ☆16Updated last month
• dami82 / mutSignatures
  mutSignatures R package - updated (dev) version - 2.1.4
  ☆14Updated 2 years ago
• etirouthier / keras_dna
  ☆23Updated 4 years ago
• bpucker / APPLS
  Applied Python Programming for Life Scientists
  ☆25Updated 4 years ago
• SziKayLeung / Whole_Transcriptome_Paper
  ☆18Updated last year
• Kuanhao-Chao / RNASeqR
  📊 An R package of RNA-seq workflow
  ☆16Updated 3 years ago
• theislab / MetaMap
  The code and analyses accompanying the manuscript “MetaMap: An atlas of metatranscriptomic reads in human disease-related RNA-seq data”.
  ☆11Updated 6 years ago
• Shicheng-Guo / HowtoBook
  Readme
  ☆10Updated 5 years ago
• openbiox / Awesome-Bioinformatics-Workflow-Chinese
  Openbiox 翻译小组发起并维护的优秀 Workflow 翻译项目
  ☆27Updated 5 years ago
• smlmbrt / SimilarityRegression
  Predicting TF sequence-specificity similarity with weighted alignments
  ☆13Updated 5 years ago
• ashleymaeconard / TIMEOR
  TIMEOR: Trajectory Inference and Mechanism Exploration with Omics Data in R
  ☆16Updated 3 years ago
• NYU-BFX / lncRNA-screen
  lncRNA-screen
  ☆25Updated 8 years ago
• griffithlab / pmbio.org
  Website for the precision medicine workshop
  ☆45Updated 6 months ago
• rkhetani / In-depth-NGS-Data-Analysis-Course
  Materials for 12-day course on analyzing RNA-Seq, ChIP-Seq and variant calling data.
  ☆16Updated 5 years ago
• crazyhottommy / compbio_resources_chatomics
  ☆27Updated last year
• genomeannotation / bioinformatics-tools
  Awk, bash, python scripts for processing NGS data
  ☆14Updated 9 years ago
• fls-bioinformatics-core / GFFUtils
  Python module and utility programs for working with GFF files
  ☆32Updated 4 years ago
• ohlerlab / RiboseQC
  Pipeline for Quality Control of Ribo-Seq data, selection of P-site offsets, and codon usage statistics.
  ☆18Updated last year
• ngs-docs / 2016-adv-begin-shell-genomics
  Workshop content for http://dib-training.readthedocs.org/en/pub/2016-01-13-adv-beg-shell.html
  ☆12Updated 7 years ago
• zhejilab / RibORF
  Identifying genome-wide translated open reading frames using ribosome profiling
  ☆23Updated last year
• s-andrews / sradownloader
  A script to make downloading of SRA/GEO data easier
  ☆30Updated last year
• ManchesterBioinference / IntegratingATAC-RNA-HiC
  scripts for the integrating ATAC-seq, RNA-seq and CHi-C paper
  ☆24Updated 2 years ago
• zd105 / AllEnricher
  A comprehensive gene set function enrichment tool for multiple species.
  ☆13Updated 5 years ago
• schatzlab / scikit-ribo
  Accurate estimation and robust modelling of translation dynamics at codon resolution
  ☆20Updated 7 years ago
• IrinaVKuznetsova / CirGO
  ☆21Updated 11 months ago