Radoje Drmanac

Summary

Publications

  1. doi request reprint Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
    Radoje Drmanac
    Complete Genomics, Inc, 2071 Stierlin Court, Mountain View, CA 94043, USA
    Science 327:78-81. 2010
  2. doi request reprint The advent of personal genome sequencing
    Radoje Drmanac
    Complete Genomics, Inc, Mountain View, California 94043, USA
    Genet Med 13:188-90. 2011
  3. ncbi request reprint Multiplexed SNP genotyping using nanobarcode particle technology
    Michael Y Sha
    Nanoplex Technologies Inc, 665 Clyde Avenue, Mountain View, CA 94043, USA
    Anal Bioanal Chem 384:658-66. 2006
  4. pmc Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
    Brock A Peters
    Complete Genomics, Inc, 2071 Stierlin Court, Mountain View, California 94043, USA
    Nature 487:190-5. 2012
  5. doi request reprint Computational techniques for human genome resequencing using mated gapped reads
    Paolo Carnevali
    Complete Genomics Inc, Mountain View, California 94043, USA
    J Comput Biol 19:279-92. 2012

Collaborators

  • Brock A Peters
  • Je Hyuk Lee
  • Paolo Carnevali
  • Michael Y Sha
  • Matt Morenzoni
  • Krishna P Pant
  • Jonathan Baccash
  • Anushka Brownley
  • Bruce Martin
  • Dennis G Ballinger
  • Aaron L Halpern
  • Geoffrey B Nilsen
  • Igor Nazarenko
  • Vitali Karpinchyk
  • Jessica C Ebert
  • Michael J Natan
  • Chongjun Xu
  • Adam Borcherding
  • Micah Taylor
  • Mark Yamanaka
  • Steve Huang
  • Sharron G Penn
  • Snezana Drmanac
  • Scott M Norton
  • Ian D Walton

Detail Information

Publications5

  1. doi request reprint Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
    Radoje Drmanac
    Complete Genomics, Inc, 2071 Stierlin Court, Mountain View, CA 94043, USA
    Science 327:78-81. 2010
    ..The high accuracy, affordable cost of $4400 for sequencing consumables, and scalability of this platform enable complete human genome sequencing for the detection of rare variants in large-scale genetic studies...
  2. doi request reprint The advent of personal genome sequencing
    Radoje Drmanac
    Complete Genomics, Inc, Mountain View, California 94043, USA
    Genet Med 13:188-90. 2011
    ....
  3. ncbi request reprint Multiplexed SNP genotyping using nanobarcode particle technology
    Michael Y Sha
    Nanoplex Technologies Inc, 665 Clyde Avenue, Mountain View, CA 94043, USA
    Anal Bioanal Chem 384:658-66. 2006
    ..To demonstrate applicability to real-world applications, 160 genotypes were determined from multiplex PCR products from 20 genomic DNA samples...
  4. pmc Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
    Brock A Peters
    Complete Genomics, Inc, 2071 Stierlin Court, Mountain View, California 94043, USA
    Nature 487:190-5. 2012
    ..Cost-effective and accurate genome sequencing and haplotyping from 10-20 human cells, as demonstrated here, will enable comprehensive genetic studies and diverse clinical applications...
  5. doi request reprint Computational techniques for human genome resequencing using mated gapped reads
    Paolo Carnevali
    Complete Genomics Inc, Mountain View, California 94043, USA
    J Comput Biol 19:279-92. 2012
    ..Finally, a correlation-based filter is applied to reduce the false positive rate caused by the presence of repetitive regions in the reference genome...