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  • I need basic help with basic questions re: analysis

    I started working on whole genome sequencing and exome sequencing with Illumina HiSeq 2000 and also with 454 sequencer. Can anybody please help me to understand the data analysis of the sequenced reads????

  • #2
    Originally posted by rd69 View Post
    I started working on whole genome sequencing and exome sequencing with Illumina HiSeq 2000 and also with 454 sequencer. Can anybody please help me to understand the data analysis of the sequenced reads????
    If you'd like answers to such a question, you should start by posting in the correct forum. Then, explain what you want to do with the reads. You're query can be condensed to "I ran an experiment; how do I analyze it?", and nobody can really help you without some real detail.

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    • #3
      Originally posted by rd69 View Post
      I started working on whole genome sequencing and exome sequencing with Illumina HiSeq 2000 and also with 454 sequencer. Can anybody please help me to understand the data analysis of the sequenced reads????
      Anyone remember the days were you just dumped 3 volumes of Maniatis on a student desk and turned around... probably not.

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      • #4
        Moved this to a new thread...and I really encourage the original poster to read the following:

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