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  • SquirrelSeq
    Member
    • May 2013
    • 10

    total RNA/transcriptome of E.coli or S.cerevisiae

    Hello everybody,

    I'm looking for a repository/archive/database, where I can download FASTQ files of NGS Deep Sequencing runs of E.coli and S.cerevisiae.

    Can anybody tell me, where I can find such data publicly available?

    Best regards,
    SquirrelSeq
  • sudhirvarma
    Junior Member
    • Jun 2012
    • 2

    #2
    SRA is the source

    Hi SquirrelSeq
    The NCBI Short Read Archive has several E. coli and S. cervisiae datasets, e.g.

    E. coli

    S. cervisiae

    They are in the "sra" format (not FASTQ) which makes the file size smaller to download. SRA has a tool that will easily convert the sra format to fastq. Use the install instructions from here. What you need is the "fastq-dump" tool

    Sudhir
    Sudhir Varma
    HiThru Analytics LLC

    Comment

    • SquirrelSeq
      Member
      • May 2013
      • 10

      #3
      Thank you for your help, that was highly useful!

      Comment

      • SquirrelSeq
        Member
        • May 2013
        • 10

        #4
        I downloaded several promising libraries.

        Some of them are documented not very detailedly. Before mapping, I normally trim adapters and primers. Are these already trimmed in the public data usually? Otherwise, how should people be able to map the sequences?
        (e.g. in 36bp short reads)

        Comment

        • TonyBrooks
          Senior Member
          • Jun 2009
          • 303

          #5
          Originally posted by SquirrelSeq View Post
          I downloaded several promising libraries.

          Some of them are documented not very detailedly. Before mapping, I normally trim adapters and primers. Are these already trimmed in the public data usually? Otherwise, how should people be able to map the sequences?
          (e.g. in 36bp short reads)
          Why not run the fastq through fastqc to check whether they even need trimming?

          Comment

          • SquirrelSeq
            Member
            • May 2013
            • 10

            #6
            That is an idea. But as far as I know, I could only see enriched sequences. Is this really enough, to identify primers/adapters? Also other sequences could be enriched, especially in specific samples, such as ribosomal RNA

            Comment

            • peter pfand
              Junior Member
              • Jan 2015
              • 1

              #7
              Is there anything similar but for microarray data?

              Thanks

              Comment

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