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  • V1.20.0

    # New feature
    - New subworkflows and process for Element's data (demultiplexStat, remove merge_lanes process, use lane number to get fastq files, ...) #96
    
    # Improvements
    - FastqScreen config file in the assets folder is use by default if no one is in the demultiplexed data folder #105
    - Workflow's names have been changed : QC_ANALYSIS -> PLAGE, ILLUMINA_QC -> SHORT_READS_QC #106
    - Illumina related NGL-Bi process have been moved into CORE_ILLUMINA sub-workflow #107
    - MD5SUM process are called with the extension of file to run on
  • V1.19.0

    # New feature and improvement
    - Add direct link to NGL-Bi in final email #103
    - Add the MultiQC report to the NGL-Bi Analysis #101
    - Add 10X subworflow with file management #5
    
    # Bug fixed
    - Fastq channel now get each file once #100
  • V1.18.0

    # Improvement and new features
    - Replace local begin_nglbi subworkflow by its in shared_modules #97
    - Add NGL-Bi Analysis creation  #98
  • V1.17.0

    # New feature 
        - Add NGL-SQ Experiement Code and NGL-Bi Run Code in emails and MultiQC
    
    # Bug fixed 
        - Qualimap reconization memory in case of decimal value
        - Little error when NGL-Bi run is created again in nextflow
  • V1.16.1

    Hot fix to get ngl-biRunCode from file
  • V1.16.0

    Improvements and New features :
    - Update sortMeRNA databases #85
    - Add Qualimap to the RNA pipeline #88
    - New way to rename files before adding them in NGL-Bi (with sequence index) #91
    
    Bugs fixed :
    - Add R dependency for picard's process #86
    - Correct the column gotten to find the GC_DROPOUT value #87
  • V1.15.0

    New features and Improvements
    - Update bwa version in fastqScreen conf file
    - Improve ressources for fastQC, Sortmerna, Qualimap, 
    - Change defaut path to shared_modules, stored on genobioinfo
    - Run Qualimap in the RNA pipeline
    - DTM mode force to keep the workdir
    
    Bug fixed
    - GC_DROPOUT value is now got from report in DTM mode
  • V1.14.0

    Merges requests : !11, !12, !13, !14
    
    New features & improvements :
    - STAR's logs are now kept #80
    - Merge of fastq files by lanes for AVITI data #79
    - Keep the wordir if DTM mode is activated #81
    - New function to manage requested ressources #84
    
    Bug fixed :
    - New default value for the lane in Treatment_demux_run (because of changes in shared_modules) #83
  • V1.10.0

    New features & improvement
    - New config for NGL-Bi related shared_modules #78
    - Add GC bias analysis process in DTM mode (performe analysis and export results in the CSV) #76
    - Multipool analysis per lane is now possible (based on multiline jFlow file) #75
    
    Bug fixed
    - New config for dev mode #77
    - Remove NA in demultiplexStat for MiSeq analysis #73
  • V1.8.0

    New features and improvements :
    - Add diversity QC subworkflow for 16s/amplicon dataset #71
    - Writing of docs/usage.md #74
    - Increase memory for seqtk sample process #72
    
    Bug fixed :
    - Replace Nas by 0 in demultiplexStat #73
  • V1.6.0

    Release: V1.6.0
    merge request : !8
    Milestone : 6
  • V1.4.0

    Release: V1.4.0
    Split CORE pipeline in two.  
    The first is especially made for data from bcl2fastq.  
    The second can be ran on every fastq files.
  • V1.2.4

    Release: V1.2.4
    Little improvements from V1.2.0
  • V1.0.0

    Merge : !2
    
    The pipeline is now ready for DNA and RTL data, if the jFlow file contains only one line.
    Other condition is : one project on the lane.
    These limitations will remove soon
    
    # New features
    - Add scripts for DTM
    - Change trim sample method in the MultiQC config file
    - Add fastq subsetting step in the CORE pipeline
    - Add email sending steps 
    - Change params case
    and more...