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The New England Journal of Medicine
|
December 25, 2015
Copy-Number Variation and False Positive Results of Prenatal Screening
Matthew W Snyder, Hilary S Gammill, Jay Shendure
Cell
|
March 23, 2019
Genomic Medicine-Progress, Pitfalls, and Promise
Jay Shendure, Gregory M Findlay, Matthew W Snyder
Nature Reviews. Genetics
|
May 8, 2015
Haplotype-resolved genome sequencing: experimental methods and applications
Matthew W Snyder, Andrew Adey, Jacob O Kitzman, et al.
NPJ Genomic Medicine
|
November 28, 2018
New insights into structural features and optimal detection of circulating tumor DNA determined by single-strand DNA analysis
Cynthia Sanchez, Matthew W Snyder, Rita Tanos, et al.
Cell
|
January 16, 2016
Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin
Matthew W Snyder, Martin Kircher, Andrew J Hill, et al.
Prenatal Diagnosis
|
April 5, 2013
Noninvasive fetal genome sequencing: a primer
Matthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
Genome Research
|
November 6, 2014
Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strains
Stephen J Salipante, David J Roach, Jacob O Kitzman, et al.
The New England Journal of Medicine
|
April 2, 2015
Copy-number variation and false positive prenatal aneuploidy screening results
Matthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
Genome Medicine
|
May 29, 2015
Whole genome prediction for preimplantation genetic diagnosis
Akash Kumar, Allison Ryan, Jacob O Kitzman, et al.
Science Translational Medicine
|
June 8, 2012
Noninvasive whole-genome sequencing of a human fetus
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, et al.
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Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
The New England Journal of Medicine
|
December 25, 2015
Copy-Number Variation and False Positive Results of Prenatal Screening
Matthew W Snyder, Hilary S Gammill, Jay Shendure
Cell
|
March 23, 2019
Genomic Medicine-Progress, Pitfalls, and Promise
Jay Shendure, Gregory M Findlay, Matthew W Snyder
Nature Reviews. Genetics
|
May 8, 2015
Haplotype-resolved genome sequencing: experimental methods and applications
Matthew W Snyder, Andrew Adey, Jacob O Kitzman, et al.
NPJ Genomic Medicine
|
November 28, 2018
New insights into structural features and optimal detection of circulating tumor DNA determined by single-strand DNA analysis
Cynthia Sanchez, Matthew W Snyder, Rita Tanos, et al.
Cell
|
January 16, 2016
Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin
Matthew W Snyder, Martin Kircher, Andrew J Hill, et al.
Prenatal Diagnosis
|
April 5, 2013
Noninvasive fetal genome sequencing: a primer
Matthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
Genome Research
|
November 6, 2014
Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strains
Stephen J Salipante, David J Roach, Jacob O Kitzman, et al.
The New England Journal of Medicine
|
April 2, 2015
Copy-number variation and false positive prenatal aneuploidy screening results
Matthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
Genome Medicine
|
May 29, 2015
Whole genome prediction for preimplantation genetic diagnosis
Akash Kumar, Allison Ryan, Jacob O Kitzman, et al.
Science Translational Medicine
|
June 8, 2012
Noninvasive whole-genome sequencing of a human fetus
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, et al.
Page
of 2