Alternatives and similar repositories for workflow-meetup

Users that are interested in workflow-meetup are comparing it to the libraries listed below

• ddbj / human-reseq
  ☆11Updated 3 years ago
• yyoshiaki / ikra
  RNAseq pipeline centered on Salmon
  ☆29Updated 10 months ago
• pitagora-network / pitagora-cwl
  Common Workflow Language tools and workflows by Pitagora-Network
  ☆33Updated 2 years ago
• pitagora-network / DAT2-cwl
  Common Workflow Language definition files for workflows introduced in DAT2
  ☆11Updated 3 years ago
• go-gts / gts
  GTS: Genome Transformation Subprograms
  ☆14Updated 2 years ago
• MoMI-G / MoMI-G
  Modular Multi-scale Integrated Genome Graph Browser
  ☆92Updated last month
• dbcls / Togothon
  ☆33Updated 3 weeks ago
• kztakemoto / network-analysis-in-biology
  「生物ネットワーク解析」の補足資料
  ☆25Updated 7 months ago
• misshie / ngsdat2
  NGS Data Analysis Textbook Version 2 (Disease Genome Analysis)
  ☆43Updated 4 years ago
• meso-cacase / GGGenome
  塩基配列を高速に検索するウェブサービス
  ☆18Updated this week
• sapporo-wes / sapporo
  A standard implementation conforming to the Global Alliance for Genomics and Health (GA4GH) Workflow Execution Service (WES) API specific…
  ☆21Updated 2 years ago
• roryk / tiny-test-data
  Super small biological datasets for unit testing
  ☆61Updated 5 years ago
• Kan-E / RNAseqChef
  Web app for automated, systematic, and integrated RNA-seq differential expression analysis
  ☆15Updated 5 months ago
• friend1ws / SAVNet
  detection of mutations causing splicing change
  ☆13Updated 2 years ago
• Genomon-Project / paplot
  paplot creates various dynamic and interactive reports for cancer genome analysis.
  ☆25Updated 2 years ago
• J35P312 / FindSV
  Structural variant pipeline
  ☆17Updated 5 years ago
• galantelab / sandy
  A straightforward and complete next-generation sequencing read simulator
  ☆21Updated last year
• yachielab / SPADE
  ☆15Updated 2 years ago
• ocxtal / minialign
  [IMPORTANT: not for real data analysis, only for algorithm evaluation] fast and accurate alignment tool for PacBio and Nanopore long read…
  ☆124Updated 7 years ago
• yachielab / FRACTAL
  FRACTAL: framework for distributed computing to trace large accurate lineages
  ☆23Updated 3 years ago
• yuifu / millefy
  Millefy: Genome browser-like visualization of single-cell RNA-seq dataset
  ☆29Updated 5 years ago
• yyoshiaki / VIRTUS
  A bioinformatics pipeline for viral transcriptome detection and quantification considering splicing.
  ☆34Updated 3 years ago
• Genomon-Project / GenomonSV
  structure detection program
  ☆17Updated 10 months ago
• galaxy-genome-annotation / docker-jbrowse
  Docker image of JBrowse Genome Browser
  ☆15Updated 4 years ago
• rgcgithub / clamms
  CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.
  ☆30Updated 4 years ago
• mkasa / klab
  Kasahara lab. public repository.
  ☆14Updated 4 months ago
• Imamachi-n / NGS-Tutorial
  NGS Tutorial
  ☆15Updated 8 years ago
• brentp / gsort
  sort genomic data
  ☆36Updated 5 years ago
• mcfrith / last-rna
  ☆49Updated 2 years ago
• dermasugita / Viola-SV
  Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.
  ☆26Updated last year