Inocras is offering whole genome sequencing for both somatic and germline samples using the power of Ultima Genomics's high-throughput UG 100, plus the ppmSeq application. As an experienced and exclusive Ultima Certified Service Provider, we're bringing you access to cost-effective and scalable sequencing and our add-on bioinformatics expertise so you can get the most out of your next sequencing or research project. Talk to one of our experts today: https://lnkd.in/dE7sH5am
Inocras Inc.
生物技术
San Diego,California 2,769 位关注者
Unlock the new era of precision health with Inocras
关于我们
Inocras is a company for whole genome sequencing, providing a comprehensive view of a patient's entire genetic profile through WGS analysis and interpretation. Focusing on cancer and rare diseases, we aspire to fundamentally change how the world treats genetically driven diseases with an unsurpassed WGS databank and an integrated platform for generating, collecting, and analyzing genomic data.
- 网站
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https://inocras.com/
Inocras Inc.的外部链接
- 所属行业
- 生物技术
- 规模
- 11-50 人
- 总部
- San Diego,California
- 类型
- 私人持股
- 创立
- 2020
- 领域
- Whole genome sequencing、WGS、cancer和rare disease
地点
Inocras Inc.员工
动态
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Inocras Inc.转发了
$80 a genome. $0.24 per million reads. If this got your attention - our Service Providers are offering a special 'AGBT-only' promotion on all Ultima services. At half the cost of other sequencing technologies on the market, stop wasting money and #keepthechange. ?? Who is eligible: AGBT attendees ?? Limited time only: project purchase order submitted ty April 30 ?? Maximum: 20 wafers at 10B reads per wafer ?? One use per customer lab ?? Mention promo codes when ordering (see below) University of Minnesota Genomics Center Ontario Institute for Cancer Research Novogene Inocras Inc. Psomagen #AGBTGM #UG100 #NGS #omics #SingleCell #Proteomics #WGS
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Inocras Inc.转发了
Great meeting between Inocras Inc. and Watchmaker Genomics at AGBT to continue our strategic collaboration for genomic innovations. Exciting results and expansion of whole genome based assays using Watchmaker's DNA Library Prep Kits with Fragmentation! Congrats to Inocras on the clinical validation of CancerVision and continued expansion into new markets.
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?? Drinks are on us! This evening and tomorrow evening from 8 PM to 11 PM, join us in Sirene Tower Suite 7012 for cocktails and conversation. We look forward to hosting you at #AGBT25.
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?? Find us in the in the Sirene Suite 7012 at #AGBT25! Swing by for a chat with our experts and join us in the evenings for food, drinks and fun! And don't forget to to pick up some sunscreen and a hat to enjoy your time in the Florida sunshine. If you'd like to set up a time to meet with our experts, please book a time: https://lnkd.in/gZN9JD4r We look forward to seeing you in Marco Island! ???
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?? Unlocking the Power of Whole Genome Sequencing At Inocras, we deliver highly sensitive genome-wide signatures that enhance our understanding of cancer genomics. Our CancerVision solution accurately detects genomic pattern-based markers, providing reliable homologous recombination deficiency (HRD) detection without the need for additional tests. In analyzing 688 cancer patient cases, CancerVision has demonstrated its ability to identify significant genomic alterations, paving the way for precision oncology and personalized treatment strategies. #CancerVision #WGS #CancerGenomics #PrecisionMedicine
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?? #AGBT25 is right around the corner! We're excited to present four scientific abstracts on Monday, February 24 at 1:30 p.m. to 3:30 p.m. ET in the Calusa Ballroom 8-12. If you'd like to schedule a time to meet with our experts, please book a time: https://lnkd.in/gZN9JD4r We look forward to seeing you in Marco Island! ???
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?? Introducing CancerVision: The Future of Cancer Genomics Our CLIA-certified, CAP-accredited CancerVision test is powered by whole genome sequencing (WGS). Along with an AI-driven interpretation pipeline created with thousands of samples, CancerVision delivers highly curated and actionable insights that empower researchers, providers and patients. What we offer: ● Target-enhanced whole genome sequencing: WGS backbone + 500x gene panel ● Comprehensive alteration detection: SNV, INDEL, CNV, SV, including variants in non-coding regions ● Advanced genomic signatures: Proprietary algorithms for TMB, MSI, HRD, and more Discover the power of genomics today. https://inocras.com/ #CancerVision #WholeGenomeSequencing #Genomics #PrecisionMedicine
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We use innovative machine-learning technology for FFPE correction (IP-protected) alongside wet lab expertise to ensure quality sample preparation. Our CancerVision platform integrates an FFPE correction algorithm, allowing precise WGS analysis despite historical challenges. Want to learn more? We'll be at #AGBT25! Stop by our?Sirene Tower Suite 7012 at the JW Marriot during on Tuesday, February 25th at 8 AM for?a coffee and informational poster presentation on our FFPE technology and so much more. If you'd like to talk one-on-one, please book a time. https://lnkd.in/g7arJAuw #CancerResearch #AI #MachineLearning #Diagnostics #AGBT25
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