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  • peter pfand
    replied
    Is there anything similar but for microarray data?

    Thanks

    Leave a comment:


  • SquirrelSeq
    replied
    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

    Leave a comment:


  • TonyBrooks
    replied
    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?

    Leave a comment:


  • SquirrelSeq
    replied
    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)

    Leave a comment:


  • SquirrelSeq
    replied
    Thank you for your help, that was highly useful!

    Leave a comment:


  • sudhirvarma
    replied
    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

    Leave a comment:


  • 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

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  • seqadmin
    Recent Advances in Sequencing Technologies
    by seqadmin



    Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

    Long-Read Sequencing
    Long-read sequencing has seen remarkable advancements,...
    12-02-2024, 01:49 PM

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