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  1. We have deep first hand experience in the area, spanning tens of thousands of reports. Technology. Our fast and nearly automated platform for small and large oncology panel reporting is based on ~10 years curation and automation. Customer Experience.

  2. We enable pharmaceutical companies with clinical data and bioinformatics solutions for target discovery, translational research and clinical research. We generate single-cell, spatial transcriptomics and genomics data from clinical samples in our India-based CAP lab.

  3. A Message FromThe CEO. Our team of 450 has over 23 years of bioinformatics experience supporting US-based genomics majors and first-hand experience in NGS-based diagnostics and clinical cohorts; we can solve your 'omics problems-rapidly and efficiently.

  4. Joining our team at Strand Life Sciences is an exciting opportunity to embark on a rewarding journey in the cutting-edge world of genetics and genomics. We pride ourselves on fostering a dynamic and collaborative work environment that encourages innovation and growth.

  5. Make Genomic Sequencing Accessible to Everyone. Our mission at Strand is to simplify the complexity of genome sequencing, thus making it accessible to everyone. We started this journey as a spin off from the Indian Institute of Science in the year 2000.

  6. Oct 25, 2024 · With streamlined workflows, powerful filtering, extensive curated content, and detailed audit logs, Strand Omics enables reliable identification of the one or two key genomic variants from the tens to hundreds of thousands found for each sample in inherited diseases cases.

  7. We leverage our expertise in omics technologies to untangle crucial insights in the fields of oncology, immunology, and drug discovery. We generate single-cell, spatial transcriptomics, and genomics data from clinical samples in our India-based CAP lab.

  8. Our mission at Strand is to simplify the complexity of genome sequencing, thus making it accessible to everyone.

  9. Mar 29, 2024 · Our mission at Strand is to simplify the complexity of genome sequencing, thus making it accessible to everyone.

  10. Like, Comment, Follow, Share & Subscribe us on our social media channels. About. Team; Journey; FAQ's; Strand Articles; Diagnostics. Genomic Wellness; Cancer Risk ...

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