Brock A Peters

Summary

Publications

  1. 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
  2. pmc Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples
    Serban Nacu
    Department of Bioinformatics and Molecular Biology, Genentech, Inc, South San Francisco, California 94080, USA
    BMC Med Genomics 4:11. 2011
  3. 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

Collaborators

Detail Information

Publications3

  1. 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...
  2. pmc Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples
    Serban Nacu
    Department of Bioinformatics and Molecular Biology, Genentech, Inc, South San Francisco, California 94080, USA
    BMC Med Genomics 4:11. 2011
    ..Deep transcriptional sequencing (RNA-Seq) now makes it possible to study the occurrence and expression levels of TICs in individual samples across the genome...
  3. 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...