Alternatives and similar repositories for terra-ui

Users that are interested in terra-ui are comparing it to the libraries listed below

• DataBiosphere / jade-data-repo
  The Terra Data Repository built by the Jade team.
  ☆13Updated last week
• broadinstitute / cromshell
  CLI for interacting with Cromwell servers
  ☆53Updated last year
• broadinstitute / cromwell-tools
  A collection of Python clients and accessory scripts for interacting with the Cromwell
  ☆22Updated 2 years ago
• stjude / CICERO
  CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data.
  ☆38Updated 3 weeks ago
• dnanexus / dxWDL
  Workflow Description Language compiler for the DNAnexus platform
  ☆40Updated last year
• broadinstitute / fiss
  FireCloud Service Selector (FISS) -- Python bindings and CLI for FireCloud execution engine
  ☆31Updated last month
• broadinstitute / wdl-ide
  Rich IDE support for Workflow Description Language
  ☆42Updated last month
• 4dn-dcic / tibanna
  Tibanna helps you run your genomic pipelines on Amazon cloud (AWS). It is used by the 4DN DCIC (4D Nucleome Data Coordination and Integr…
  ☆69Updated last month
• stjudecloud / workflows
  Bioinformatics workflows developed for and used on the St. Jude Cloud project.
  ☆36Updated this week
• gatk-workflows / seq-format-conversion
  Workflows for converting between sequence data formats
  ☆38Updated 3 years ago
• Illumina / GraphAlignmentViewer
  ☆35Updated 3 years ago
• Wedge-lab / battenberg
  Battenberg R package for subclonal copynumber estimation
  ☆86Updated last month
• gatk-workflows / five-dollar-genome-analysis-pipeline
  Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline
  ☆57Updated 5 years ago
• lidaof / eg-react
  WashU Epigenome Browser
  ☆73Updated last month
• broadinstitute / long-read-pipelines
  Long read production pipelines
  ☆145Updated last week
• hms-dbmi / chromoscope
  Interactive multiscale visualization for structural variation in human genomes
  ☆68Updated this week
• cancerit / ascatNgs
  Somatic copy number analysis using WGS paired end wholegenome sequencing
  ☆71Updated 4 years ago
• gogetdata / ggd-recipes
  conda recipes for genomic data
  ☆85Updated 3 years ago
• SciLifeLab / TIDDIT
  TIDDIT - structural variant calling
  ☆73Updated last month
• WGLab / NanoCaller
  Variant calling tool for long-read sequencing data
  ☆109Updated last month
• FusionInspector / FusionInspector
  FusionInspector code
  ☆57Updated 6 months ago
• NCBI-Hackathons / Community_Software_Tools_for_NGS
  ☆62Updated 8 years ago
• human-pangenomics / hpp_pangenome_resources
  ☆111Updated last year
• broadinstitute / gnomad_qc
  ☆69Updated this week
• Ensembl / ensembl-analysis
  Modules to interface with tools used in Ensembl Gene Annotation Process and scripts to run pipelines
  ☆18Updated this week
• NCI-GDC / gdc-dnaseq-cwl
  CWL for GDC DNASeq workflows
  ☆22Updated last week
• gatk-workflows / gatk4-genome-processing-pipeline
  Workflows used for processing whole genome sequence data + germline variant calling. This Repository has been archived, please visit the …
  ☆28Updated 4 years ago
• human-pangenomics / HG002_Data_Freeze_v1.0
  Human Pangenome Reference Consortium - HG002 Data Freeze (v1.0)
  ☆79Updated 2 years ago
• mskilab-org / JaBbA
  MIP based joint inference of copy number and rearrangement state in cancer whole genome sequence data.
  ☆56Updated last month
• Magdoll / Cogent
  Coding Genome Reconstruction using Iso-Seq data
  ☆61Updated 3 years ago