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The bioinformatics unit provides several services for obtaining NGS data.  The entire process can be divided into 2 main steps - 

  1. Sequencing to sequences - services that assist with retrieving raw fastq or demultiplexed files as well as quality control measures for each sample that was sequenced
    1. Sequencing setup

    2. Additional From samples to analyzed NGS data & UTAP#Sequencing setup

    3. From samples to analyzed NGS data & UTAP#Additional services for sequences

  2. UTAP: User-friendly Transcriptome Analysis Pipeline

    1. Analysis From samples to analyzed NGS data & UTAP#Analysis setup BEFORE sequencing completion
    2. Analysis From samples to analyzed NGS data & UTAP#Analysis setup AFTER sequencing completion
    3. Analysis From samples to analyzed NGS data & UTAP#Analysis pipeline steps and reports - an automatic pipeline for analyzing transcriptome data

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http://stefan.weizmann.ac.il/fqc/{type RUN ID here}

For example:

http://stefan.weizmann.ac.il/raw/180509_NB551168_0120_AHTKN2BGX5/

List of runs and Deleting run:

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