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Home / References
QUATITATIVE DIGITAL PCR Beer NR, Wheeler EK, Lee-Houghton L,
Watkins N, Nasarabadi
S, Hebert N, Leung P, Arnold DW, Bailey CG, Colston BW.
On-chip
single-copy real-time reverse-transcription PCR in isolated picoliter
droplets.
Anal Chem. 2008 Mar 15;80(6):1854-8. Diehl F, Schmidt K, Durkee KH, Moore KJ,
Goodman SN,
Shuber AP, Kinzler KW, Vogelstein B. Analysis of mutations
in DNA
isolated from plasma and stool of colorectal cancer patients.
Gastroenterology.
2008 Aug;135(2):489-98. Epub 2008 May 15. Dube S, Qin J, Ramakrishnan R.
Mathematical
analysis of copy number variation in a DNA sample using digital PCR on
a
nanofluidic device. PLoS ONE. 2008 Aug 6;3(8):e2876. Lun FM, Chiu RW, Chan KC, Leung TY, Lau TK,
Lo YM.
Microfluidics Digital PCR Reveals a Higher than Expected Fraction of
Fetal DNA
in Maternal Plasma. Clin Chem. 2008 Aug 14. McCaughan F, Darai-Ramqvist E, Bankier A,
Konfortov B,
Foster N, George P, Rabbitts T, Kost-Alimova M, Rabbitts P, Dear P. Microdissection molecular copy-number
counting (microMCC)-unlocking cancer archives with digital PCR. J
Pathol. 2008
Jul 29. Qin J, Jones RC, Ramakrishnan R.
Studying
copy number variations using a nanofluidic platform. Nucleic Acids Res.
2008
Aug 18. Weisenberger DJ, Trinh BN, Campan M, Sharma
S, Long
TI, Ananthnarayan S, Liang G, Esteva FJ, Hortobagyi GN, McCormick F,
Jones PA,
Laird PW. DNA methylation analysis by digital bisulfite
genomic
sequencing and digital MethyLight. Nucleic Acids Res. 2008 Aug;36(14):4689-98. Diehl F, Diaz LA Jr. Digital quantification of mutant DNA in
cancer patients. Curr Opin Oncol. 2007 Jan;19(1):36-42. Rago C, Huso DL, Diehl F, Karim B, Liu G,
Papadopoulos
N, Samuels Y, Velculescu VE, Vogelstein B, Kinzler KW, Diaz LA Jr.
Serial assessment of human tumor burdens in mice by the analysis of
circulating
DNA. Cancer Res. 2007 Oct 1;67(19):9364-70. Schmidt K, Diehl F. A
blood-based DNA test
for colorectal cancer screening. Discov Med. 2007 Feb;7(37):7-12. Li M, Diehl F, Dressman D, Vogelstein B,
Kinzler KW.
BEAMing up for detection and quantification of rare sequence variants.
Nat
Methods. 2006 Feb;3(2):95-7. Ottesen EA, Hong JW, Quake SR, Leadbetter
JR.
Microfluidic digital PCR enables multigene analysis of individual
environmental
bacteria. Science. 2006 Dec 1;314(5804):1464-7. Rübben A, Bausch B, Nikkels A.
Somatic
deletion of the NF1 gene in a neurofibromatosis type 1-associated
malignant
melanoma demonstrated by digital PCR. Mol Cancer. 2006 Sep 10;5:36. Matsubara Y, Kerman K, Kobayashi M,
Yamamura S, Morita
Y, Tamiya E. Microchamber array based DNA quantification and
specific sequence detection from a single copy via PCR in nanoliter
volumes.
Biosens Bioelectron. 2005 Feb 15;20(8):1482-90. Matsubara Y, Kerman K, Kobayashi M,
Yamamura S, Morita
Y, Takamura Y, Tamiya E. On-chip nanoliter-volume multiplex
TaqMan
polymerase chain reaction from a single copy based on counting
fluorescence released
microchambers. Anal Chem. 2004 Nov
1;76(21):6434-9. Pohl G, Shih IeM. Principle and applications of digital PCR. Expert Rev Mol Diagn. 2004 Jan;4(1):41-7. Traverso G, Shuber A, Levin B, Johnson C, Olsson L, Schoetz DJ Jr, Hamilton SR, Boynton K, Kinzler KW, Vogelstein B. Detection of APC mutations in fecal DNA from patients with colorectal tumors. N Engl J Med. 2002 Jan 31;346(5):311-20. Dong SM, Traverso G, Johnson C, Geng L,
Favis R,
Boynton K, Hibi K, Goodman SN, D'Allessio M, Paty P, Hamilton SR,
Sidransky D,
Barany F, Levin B, Shuber A, Kinzler KW, Vogelstein B, Jen J.
Detecting colorectal cancer in stool with the use of multiple genetic
targets.
J Natl Cancer Inst. 2001 Jun 6;93(11):858-65. Zhou W, Galizia G, Lieto E, Goodman SN,
Romans KE,
Kinzler KW, Vogelstein B, Choti MA, Montgomery EA. Counting
alleles
reveals a connection between chromosome 18q loss and vascular invasion.
Nat
Biotechnol. 2001 Jan;19(1):78-81. Erratum in: Nat Biotechnol 2001
Mar;19(3):277. Vogelstein B, Kinzler KW.
Digital PCR. Proc
Natl Acad Sci U S A. 1999 Aug 3;96(16):9236-41.
Home /
References SECOND
GENERATION SEQUENCING Droege M, Hill B. The Genome
Sequencer
FLXtrade mark System-Longer reads, more applications, straight forward
bioinformatics and more complete data sets. J Biotechnol. 2008 Aug 31;136(1-2):3-10. Huang W, Marth G. EagleView: a
genome assembly
viewer for next-generation sequencing technologies. Genome Res. 2008
Sep;18(9):1538-43. Smith AD, Xuan Z, Zhang MQ.
Using quality
scores and longer reads improves accuracy of Solexa read mapping. BMC
Bioinformatics. 2008 Feb 28;9:128. Issued Patents Published Patent Applications Home / References
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