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Frontiers in Molecular Biosciences
|
September 25, 2023
A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction
Emma Bohn, Tammy T Y Lau, Omar Wagih, et al.
Scientific Reports
|
May 8, 2021
Ubiquitin-mediated DNA damage response is synthetic lethal with G-quadruplex stabilizer CX-5461
Tehmina Masud, Charles Soong, Hong Xu, et al.
Human Molecular Genetics
|
December 15, 2010
A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis
Cheryl Jacobs, Ying Huang, Tehmina Masud, et al.
Blood
|
January 8, 2009
Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation
William Giblin, Monalisa Chatterji, Gerwin Westfield, et al.
Human Molecular Genetics
|
May 31, 2012
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
Lev Prasov, Tehmina Masud, Shagufta Khaliq, et al.
Plos Computational Biology
|
September 23, 2020
Epiclomal: Probabilistic clustering of sparse single-cell DNA methylation data
Camila P E de Souza, Mirela Andronescu, Tehmina Masud, et al.
Nature
|
June 24, 2021
Clonal fitness inferred from time-series modelling of single-cell cancer genomes
Sohrab Salehi, Farhia Kabeer, Nicholas Ceglia, et al.
Nature Genetics
|
May 17, 2016
Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer
Andrew McPherson, Andrew Roth, Emma Laks, et al.
Cell
|
November 16, 2019
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Emma Laks, Andrew McPherson, Hans Zahn, et al.
Nature
|
October 26, 2022
Single-cell genomic variation induced by mutational processes in cancer
Tyler Funnell, Ciara H O'Flanagan, Marc J Williams, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Frontiers in Molecular Biosciences
|
September 25, 2023
A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction
Emma Bohn, Tammy T Y Lau, Omar Wagih, et al.
Scientific Reports
|
May 8, 2021
Ubiquitin-mediated DNA damage response is synthetic lethal with G-quadruplex stabilizer CX-5461
Tehmina Masud, Charles Soong, Hong Xu, et al.
Human Molecular Genetics
|
December 15, 2010
A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis
Cheryl Jacobs, Ying Huang, Tehmina Masud, et al.
Blood
|
January 8, 2009
Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation
William Giblin, Monalisa Chatterji, Gerwin Westfield, et al.
Human Molecular Genetics
|
May 31, 2012
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
Lev Prasov, Tehmina Masud, Shagufta Khaliq, et al.
Plos Computational Biology
|
September 23, 2020
Epiclomal: Probabilistic clustering of sparse single-cell DNA methylation data
Camila P E de Souza, Mirela Andronescu, Tehmina Masud, et al.
Nature
|
June 24, 2021
Clonal fitness inferred from time-series modelling of single-cell cancer genomes
Sohrab Salehi, Farhia Kabeer, Nicholas Ceglia, et al.
Nature Genetics
|
May 17, 2016
Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer
Andrew McPherson, Andrew Roth, Emma Laks, et al.
Cell
|
November 16, 2019
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Emma Laks, Andrew McPherson, Hans Zahn, et al.
Nature
|
October 26, 2022
Single-cell genomic variation induced by mutational processes in cancer
Tyler Funnell, Ciara H O'Flanagan, Marc J Williams, et al.
Page
of 1