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This repository has been archived by the owner on Jun 13, 2023. It is now read-only.

Releases: imperial-genomics-facility/igf-pipelines

Mini release 2020 Jan - Notebook runner

28 Jan 12:38
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  • Replaced Scanpy report for single cell data analysis with a notebook template

Mini release 2020 Jan - wgs

15 Jan 14:23
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List of changes

  • Added GATK BQSR and HaplotypeCaller GVCF step for alignment pipeline

Pipeline improvements 2020 Jan

13 Jan 11:13
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List of new improvements:

  • changed jobmode of cellranger pipeline from PBSpro to single node
  • fixed the remote dir permission issues and enabled UCSC cellbrowser in the primary analysis pipeline

Pipeline improvements 201906

25 Jun 13:28
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List of new improvements:

  • Optimized Ehive pipeline for resource usage and job counts
  • New Epigenome QC pipeline with PPQT and Deeptools plots
  • New RNA-Seq QC pipeline (with experimental batch effect checking)
  • Cellranger for single cell and single nuclei samples
  • Scanpy report with 3D UMAP plot for single cell and single nuclei samples
  • Bcl2Fastq mask-short-adapter-reads param reset for short read cycles
  • Updated doc template
  • Using conda yaml file for travis-ci
  • Indexing cram output before iRODS upload
  • Minor changes added to the metadata db schema
  • Fixed security issues for sqlalchemy and jinja versions
  • Added a histogram plot in analysis QC page for alignment stats

Pipeline improvements

25 Apr 10:30
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  • Python wrapper scripts moved to data-management-python repo

Single cell demultiplexing pipeline

13 Apr 15:39
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This release contains the codes required for running the demultiplexing pipeline for single cell runs.

Demultiplexing pipeline

14 Mar 10:47
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First version of the demuliplexing pipeline.

Initial release

30 Jan 11:54
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Its the first release of the pipeline codebase.