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DIPLOID.COM

Diploid - Diagnosing Rare Diseases

Diploid Human Genome Interpretation. Some of the world’s best hospitals and labs are using our interpretation service and software. We provide services and software. To diagnose rare diseases. Reduce your workload and improve diagnostic rates by outsourcing clinical genome interpretation. More about Diploid services. Moon is the first software to autonomously diagnose rare diseases using artificial intelligence. More about Moon software. Prof dr. Geert Mortier, MD. Chairman, Department of Medical Genetics.

http://www.diploid.com/

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Diploid Human Genome Interpretation. Some of the world’s best hospitals and labs are using our interpretation service and software. We provide services and software. To diagnose rare diseases. Reduce your workload and improve diagnostic rates by outsourcing clinical genome interpretation. More about Diploid services. Moon is the first software to autonomously diagnose rare diseases using artificial intelligence. More about Moon software. Prof dr. Geert Mortier, MD. Chairman, Department of Medical Genetics.
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Diploid - Diagnosing Rare Diseases | diploid.com Reviews

https://diploid.com

Diploid Human Genome Interpretation. Some of the world’s best hospitals and labs are using our interpretation service and software. We provide services and software. To diagnose rare diseases. Reduce your workload and improve diagnostic rates by outsourcing clinical genome interpretation. More about Diploid services. Moon is the first software to autonomously diagnose rare diseases using artificial intelligence. More about Moon software. Prof dr. Geert Mortier, MD. Chairman, Department of Medical Genetics.

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Diploid - Diagnosing Rare Diseases

http://www.diploid.com/scientificboard

Prof Dr. Koen Kas. Prof Dr. Andrea Nemeth. Mala Isrie, MD. Sign up for our newsletter.

2

Diploid - Diagnosing Rare Diseases

http://www.diploid.com/about

Diploid wants to revolutionize healthcare by bringing genome diagnostics into daily clinical practice. With a focus on rare diseases, we analyze human genomes and communicate results that are actionable for healthcare professionals and patients. To achieve this goal we bring together expertise in human genetics, software development, and design. Peter Schols, CEO. Catheleyne D'hondt, CFO. Aimé Lumaka Zola, CMO. Cyrielle Kint, CSO. Eva Sammels, CSO. Winnie Trekker, CDO. Sign up for our newsletter.

3

Diploid - Diagnosing Rare Diseases

http://www.diploid.com/press

Jul 14, 2016. InHelix integrates with Face2Gene to improve CNV analysis. InHelix is the first CNV analysis software that has been designed from the ground up to handle the large amount of data generated by genome-wide NGS-based CNV detection. This allows InHelix to offer live filtering and smart prioritisation of CNVs, quickly guiding geneticists to the most relevant CNVs for a particular patient. Website: http:/ www.diploid.com/inhelix. Http:/ www.diploid.com. 1 855-855-6501 (US toll free number). We th...

4

Diploid - Diagnosing Rare Diseases

http://www.diploid.com/jobs

In addition to joining a talented team of doers, you'll benefit from our awesome office space, free lunches and drinks, two teleworking days, and an on-site bike repair service. Most importantly, you'll get to solve problems that will save people's lives. Sign up for our newsletter.

5

Diploid - Diagnosing Rare Diseases

http://www.diploid.com/differ

Browse, search, split and. With Differ, Diploid delivers such a tool to the community, free of charge. Opening a 1.5 GB VCF file in a text editor can take a while, even on modern computers. Differ opens these VCFs in a second or two on any modern Mac*. You’ll notice the difference. SSD recommended for optimal performance. If your VCF has been annotated with SnpEff, Differ shows the SnpEff annotations in a separate table, allowing you to search variants by gene name or effect. Split VCFs in a split second.

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Get your whole genome sequenced — Genomix

https://www.genomix.co/get-your-genome-sequenced

Get your whole genome sequenced. Whole Genome Sequencing Pre-order. Data on all 3 billion base pairs of your DNA. Research use raw data to make your own discoveries on your genome. In the event sign up numbers are not met, we will inform you via email or phone and fully refund your payment to the credit card you made payment with. WHY WHOLE GENOME SEQUENCING? Small duplications, insertions, deletions, indels. Exon duplications, deletions or gene copy number changes. WHAT INFORMATION DO I GET? Step 2: If ...

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会社概要 ::フィルジェン株式会社::

http://www.filgen.jp/Profile/Profile.htm

フィルジェン株式会社 Filgen, Inc. Phone 052-624-4388 Fax 052-624-4389 http:/ www.filgen.jp. 酒井 宏 株 竹代の代表取締役会長. 浦 榮子 株 竹代の代表取締役社長. フットサルクラブ Filgen FC 男女混合. AB SCIEX Triple TOF 5600 System. ThermoFisher TSQ Quantum Ultra(MS Bioworks社設備). ThermoFisher Orbitrap Velos Pro tandem mass spectrometer MS Bioworks社設備. ThermoFisher Q Exactive hybrid quadrupole-Orbitrap mass spectrometer MS Bioworks社設備. Waters NanoAcquity liquid chromatography system(MS Bioworks社設備). MassARRAY System Feng Chi Biotech社設備. Mind the Byte社 スペイン.

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ビジネスパートナー ::フィルジェン株式会社::

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Structure Probe, Inc. Http:/ www.2spi.com/. Beijing Hanatake Science And Technology Co.,Ltd 北京華竹科技有限公司. Http:/ hanatake.com.cn/jp/index.php. Joo Won Industrial Co.,Ltd 株式会社周元. Http:/ joowon.en.ec21.com/. 101Bioのホームページ http:/ www.101bio.com/index.php. フィルジェンの該当ページ http:/ www.filgen.jp/Product/Bioscience4/101Bio/index.html. ABclonalのホームページ http:/ www.abclonal.com/. フィルジェンの該当ページ http:/ www.filgen.jp/Product/Bioscience4/ABclonal/index.html. AC Diagnostics社 アメリカ の全製品について、日本国内における販売代理店契約を締結しております。 フィルジェンの該当ページ...

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Diploid - Diagnosing Rare Diseases

Diploid Human Genome Interpretation. Some of the world’s best hospitals and labs are using our interpretation service and software. We provide services and software. To diagnose rare diseases. Reduce your workload and improve diagnostic rates by outsourcing clinical genome interpretation. More about Diploid services. Moon is the first software to autonomously diagnose rare diseases using artificial intelligence. More about Moon software. Prof dr. Geert Mortier, MD. Chairman, Department of Medical Genetics.

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