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Gabor T Marth

Showing results (51-60 of 61) with videos related to

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Nature Methods|January 22, 2008
Whole-genome sequencing and variant discovery in C. elegansLaDeana W Hillier, Gabor T Marth, Aaron R Quinlan, et al.
Plos Genetics|August 31, 2011
A comprehensive map of mobile element insertion polymorphisms in humansChip Stewart, Deniz Kural, Michael P Strömberg, et al.
Genome Research|September 9, 2008
Rapid whole-genome mutational profiling using next-generation sequencing technologiesDouglas R Smith, Aaron R Quinlan, Heather E Peckham, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read dataYoo-Jin Jiny Ha, Dominika Maziec, Julia Markowski, et al.
Nature Cancer|February 28, 2022
A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncologyKatrin P Guillen, Maihi Fujita, Andrew J Butterfield, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Nature Methods|January 22, 2008
Whole-genome sequencing and variant discovery in C. elegansLaDeana W Hillier, Gabor T Marth, Aaron R Quinlan, et al.
Plos Genetics|August 31, 2011
A comprehensive map of mobile element insertion polymorphisms in humansChip Stewart, Deniz Kural, Michael P Strömberg, et al.
Genome Research|September 9, 2008
Rapid whole-genome mutational profiling using next-generation sequencing technologiesDouglas R Smith, Aaron R Quinlan, Heather E Peckham, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read dataYoo-Jin Jiny Ha, Dominika Maziec, Julia Markowski, et al.
Nature Cancer|February 28, 2022
A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncologyKatrin P Guillen, Maihi Fujita, Andrew J Butterfield, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Pageof 7