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  • dkrtndhkd
    Member
    • Jan 2012
    • 42

    SIFT - how recognize reference seq?

    1. when predicting nsSNV, how can the tools recognize the reference sequence? the reference file in program or input sequence i gave?

    i'm doing research about normal-tumor cancer sequence comparison,

    and i'm planning to input normal base as reference and tumor base as input data at each position where i'm interested in.

    2. is there any other good idea or tools for analyzing Normal-Tumor pair sequence?

    HELP!!!! please

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  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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  • SEQadmin2
    Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by SEQadmin2


    I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

    Here are nine questions we think about, in roughly the order they matter, before...
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