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T Marth

Showing results (71-80 of 104) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 7, 2011
Demographic history and rare allele sharing among human populationsSimon Gravel, Brenna M Henn, Ryan N Gutenkunst, et al.
Nature|November 7, 2012
An integrated map of genetic variation from 1,092 human genomes, Goncalo R Abecasis, Adam Auton, et al.
Blood|April 27, 2022
Subclonal evolution of CLL driver mutations is associated with relapse in ibrutinib- and acalabrutinib-treated patientsGage S Black, Xiaomeng Huang, Yi Qiao, et al.
Genome Biology and Evolution|March 25, 2010
Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogasterTimothy B Sackton, Rob J Kulathinal, Casey M Bergman, et al.
Nature Genetics|December 2, 1999
A general approach to single-nucleotide polymorphism discoveryG T Marth, I Korf, M D Yandell, et al.
Nature Methods|August 11, 2015
SpeedSeq: ultra-fast personal genome analysis and interpretationColby Chiang, Ryan M Layer, Gregory G Faust, et al.
Blood Cancer Journal|October 14, 2024
Clonal dynamics of aggressive systemic mastocytosis on avapritinib therapyXiaomeng Huang, Anthony D Pomicter, Jonathan Ahmann, et al.
Plos One|July 26, 2018
Automated size selection for short cell-free DNA fragments enriches for circulating tumor DNA and improves error correction during next generation sequencingSabine Hellwig, David A Nix, Keith M Gligorich, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Single-cell RNA sequencing in Hirschsprung's disease tissues reveals lack of neuronal differentiation in the aganglionic colon segmentSzabolcs Tarapcsak, Xiaomeng Huang, Yi Qiao, et al.
Genome Research|January 9, 2024
A Bayesian framework to study tumor subclone-specific expression by combining bulk DNA and single-cell RNA sequencing dataYi Qiao, Xiaomeng Huang, Philip J Moos, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2011
Demographic history and rare allele sharing among human populationsSimon Gravel, Brenna M Henn, Ryan N Gutenkunst, et al.
Nature|November 7, 2012
An integrated map of genetic variation from 1,092 human genomes, Goncalo R Abecasis, Adam Auton, et al.
Blood|April 27, 2022
Subclonal evolution of CLL driver mutations is associated with relapse in ibrutinib- and acalabrutinib-treated patientsGage S Black, Xiaomeng Huang, Yi Qiao, et al.
Genome Biology and Evolution|March 25, 2010
Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogasterTimothy B Sackton, Rob J Kulathinal, Casey M Bergman, et al.
Nature Genetics|December 2, 1999
A general approach to single-nucleotide polymorphism discoveryG T Marth, I Korf, M D Yandell, et al.
Nature Methods|August 11, 2015
SpeedSeq: ultra-fast personal genome analysis and interpretationColby Chiang, Ryan M Layer, Gregory G Faust, et al.
Blood Cancer Journal|October 14, 2024
Clonal dynamics of aggressive systemic mastocytosis on avapritinib therapyXiaomeng Huang, Anthony D Pomicter, Jonathan Ahmann, et al.
Plos One|July 26, 2018
Automated size selection for short cell-free DNA fragments enriches for circulating tumor DNA and improves error correction during next generation sequencingSabine Hellwig, David A Nix, Keith M Gligorich, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Single-cell RNA sequencing in Hirschsprung's disease tissues reveals lack of neuronal differentiation in the aganglionic colon segmentSzabolcs Tarapcsak, Xiaomeng Huang, Yi Qiao, et al.
Genome Research|January 9, 2024
A Bayesian framework to study tumor subclone-specific expression by combining bulk DNA and single-cell RNA sequencing dataYi Qiao, Xiaomeng Huang, Philip J Moos, et al.
Pageof 11