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Thread: Genos Whole Exome Sequencing for $399

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    Genos Whole Exome Sequencing for $399

    Interesting business model and analytic tools.

    OWN YOUR DNA

    Purchase a DNA kit and discover your exome, which is the most revealing part of your genome. Explore your genetic variants and associated conditions. Access certified genetic counselors for personalized consultations.

    LEAD EXPLORATION

    Browse inspiring and cutting edge research being conducted on the Genos platform. For studies of interest, choose to share your data with distinguished researchers. Studies will begin in Fall 2016.

    RECEIVE COMPENSATION

    You will be fairly compensated for sharing data thatís rightly yours when researchers accept your request to participate in a study.

    https://www.genosresearch.com/genomeintro.html
    Gerard Corcoran
    R1b-DF21-S5456-S6166, H1C1

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    Anyone done this yet? The thing that puts me off whole genome or exome sequencing is that there doesn't seem to be the same wealth of analytical tools that are available to 23andme and ftdna users (Gedmatch, interpretome, DIYDodecad etc etc).So (from an ancestry standpoint), would having all of that raw DNA available be of any use at the moment?
    Last edited by tippy; 06-15-2016 at 11:58 AM.

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    It is not yet available to international customers.
    I contacted them regarding Y, mtDNA and AIM coverage although I suspect it is a health only product.
    You can see a preview of analytics here.

    https://www.genosresearch.com/genomeintro.html
    Gerard Corcoran
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    In that case hopefully they'll start offering it to internationals like 23andme did early on (hefty fedex shipping costs but never mind). I also hope that we soon get an ancestry offering too.

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    Interesting. So, do they permit one to access their results in such a way that it can be sent to third parties for further analysis?

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    Quote Originally Posted by leonardo View Post
    Interesting. So, do they permit one to access their results in such a way that it can be sent to third parties for further analysis?
    From the FAQ.

    Can I download my genomic data?

    You can download your genomic data at any point as a VCF (variant call format) file. This large file stores all your gene sequence variations. Once you’ve been sequenced through Genos, this file will be available through the Genome explorer, as part of your Variant Report. We’ve improved our capabilities since Genos Alpha. If you participated in Genos Alpha during 2015 and would like your VCF file, please email [email protected].
    Gerard Corcoran
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    Quote Originally Posted by Heber View Post
    From the FAQ.

    Can I download my genomic data?

    You can download your genomic data at any point as a VCF (variant call format) file. This large file stores all your gene sequence variations. Once you’ve been sequenced through Genos, this file will be available through the Genome explorer, as part of your Variant Report. We’ve improved our capabilities since Genos Alpha. If you participated in Genos Alpha during 2015 and would like your VCF file, please email [email protected].
    Excuse my ignorance, would this serve like the BAM file, whereby it can be submitted to a place like YFULL? Can one gather y-dna/mtdna and find comparative matches?

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    It is not available in Florida and New York. In live in Florida and wouldn't accept order.

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    This should be in the Other section:

    http://www.anthrogenica.com/forumdisplay.php?140-Other

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    Quote Originally Posted by leonardo View Post
    Excuse my ignorance, would this serve like the BAM file, whereby it can be submitted to a place like YFULL? Can one gather y-dna/mtdna and find comparative matches?
    The exome is the parts of your genome containing genes; most of the Y SNPs are outside genes although some are inside (M222 being a notable example of the latter, in the USP9Y gene).

    YFull analyse BAM or FASTQ file data. A VCF file is a report from a SNP caller run against BAM or equivalent data so I don't believe they would use it.
    YSEQ:#37; YFull: YF01405 (Y Elite 2013)
    WGS (Full Genomes Nov 2015, YSEQ Feb 2019, Dante Mar 2019, FGC-10X Linked Reads Apr 2019, Dante-Nanopore May 2019, Chronomics Jan 2020, Sano Genetics Feb 2020, Nebula Genomics June 2020)
    Ancestry GCs: Scots in central Scotland & Ulster, Ireland; English in Yorkshire & Pennines
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    FBIMatch: A------ (autosomal DNA) for segment matching DO NOT POST ADMIXTURE REPORTS USING MY KIT

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