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Andrew B Sparks

Showing results (1-10 of 9) with videos related to

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Cancer Research|October 5, 2016
β-Catenin Mutations: Insights into the APC Pathway and the Power of GeneticsPatrice J Morin, Kenneth W Kinzler, Andrew B Sparks
American Journal of Obstetrics and Gynecology|April 3, 2012
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18Andrew B Sparks, Craig A Struble, Eric T Wang, et al.
Nature Biotechnology|May 1, 2002
Using the transcriptome to annotate the genomeSaurabh Saha, Andrew B Sparks, Carlo Rago, et al.
Prenatal Diagnosis|January 7, 2012
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomyAndrew B Sparks, Eric T Wang, Craig A Struble, et al.
American Journal of Obstetrics and Gynecology|June 30, 2012
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18Mary E Norton, Herb Brar, Jonathan Weiss, et al.
Nature|May 28, 2010
The mutation spectrum revealed by paired genome sequences from a lung cancer patientWilliam Lee, Zhaoshi Jiang, Jinfeng Liu, et al.
Nature|July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cellsBrock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Science (New York, N.Y.)|October 13, 2007
The genomic landscapes of human breast and colorectal cancersLaura D Wood, D Williams Parsons, Siân Jones, et al.
Science (New York, N.Y.)|November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarraysRadoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Cancer Research|October 5, 2016
β-Catenin Mutations: Insights into the APC Pathway and the Power of GeneticsPatrice J Morin, Kenneth W Kinzler, Andrew B Sparks
American Journal of Obstetrics and Gynecology|April 3, 2012
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18Andrew B Sparks, Craig A Struble, Eric T Wang, et al.
Nature Biotechnology|May 1, 2002
Using the transcriptome to annotate the genomeSaurabh Saha, Andrew B Sparks, Carlo Rago, et al.
Prenatal Diagnosis|January 7, 2012
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomyAndrew B Sparks, Eric T Wang, Craig A Struble, et al.
American Journal of Obstetrics and Gynecology|June 30, 2012
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18Mary E Norton, Herb Brar, Jonathan Weiss, et al.
Nature|May 28, 2010
The mutation spectrum revealed by paired genome sequences from a lung cancer patientWilliam Lee, Zhaoshi Jiang, Jinfeng Liu, et al.
Nature|July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cellsBrock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Science (New York, N.Y.)|October 13, 2007
The genomic landscapes of human breast and colorectal cancersLaura D Wood, D Williams Parsons, Siân Jones, et al.
Science (New York, N.Y.)|November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarraysRadoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
Pageof 1