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Nature Communications
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August 21, 2014
Identification of genetic variants associated with alternative splicing using sQTLseekeR
Jean Monlong, Miquel Calvo, Pedro G Ferreira, et al.
Veterinary Research
|
June 26, 2024
Mapping the scientific output of organoids for animal and human modeling infectious diseases: a bibliometric assessment
Jin Yan, Jean Monlong, Céline Cougoule, et al.
BMJ (Clinical Research Ed.)
|
November 25, 2011
Overdiagnosis from non-progressive cancer detected by screening mammography: stochastic simulation study with calibration to population based registry data
Arnaud Seigneurin, Olivier François, José Labarère, et al.
Nucleic Acids Research
|
August 24, 2018
Human copy number variants are enriched in regions of low mappability
Jean Monlong, Patrick Cossette, Caroline Meloche, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 30, 2021
Inferring Copy Number from Triple-Negative Breast Cancer Patient Derived Xenograft scRNAseq Data Using scCNA
Elena Kuzmin, Jean Monlong, Constanza Martinez, et al.
Nature Biotechnology
|
May 10, 2023
Pangenome graph construction from genome alignments with Minigraph-Cactus
Glenn Hickey, Jean Monlong, Jana Ebler, et al.
Biorxiv : the Preprint Server for Biology
|
October 28, 2024
Efficient indexing and querying of annotations in a pangenome graph
Adam M Novak, Dickson Chung, Glenn Hickey, et al.
Genome Biology
|
February 14, 2020
Genotyping structural variants in pangenome graphs using the vg toolkit
Glenn Hickey, David Heller, Jean Monlong, et al.
Nature Communications
|
October 26, 2019
Genome-wide microhomologies enable precise template-free editing of biologically relevant deletion mutations
Janin Grajcarek, Jean Monlong, Yoko Nishinaka-Arai, et al.
Nature Methods
|
September 11, 2024
Personalized pangenome references
Jouni Sirén, Parsa Eskandar, Matteo Tommaso Ungaro, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 43) with videos related to
Sort By:
Page
of 5
Nature Communications
|
August 21, 2014
Identification of genetic variants associated with alternative splicing using sQTLseekeR
Jean Monlong, Miquel Calvo, Pedro G Ferreira, et al.
Veterinary Research
|
June 26, 2024
Mapping the scientific output of organoids for animal and human modeling infectious diseases: a bibliometric assessment
Jin Yan, Jean Monlong, Céline Cougoule, et al.
BMJ (Clinical Research Ed.)
|
November 25, 2011
Overdiagnosis from non-progressive cancer detected by screening mammography: stochastic simulation study with calibration to population based registry data
Arnaud Seigneurin, Olivier François, José Labarère, et al.
Nucleic Acids Research
|
August 24, 2018
Human copy number variants are enriched in regions of low mappability
Jean Monlong, Patrick Cossette, Caroline Meloche, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 30, 2021
Inferring Copy Number from Triple-Negative Breast Cancer Patient Derived Xenograft scRNAseq Data Using scCNA
Elena Kuzmin, Jean Monlong, Constanza Martinez, et al.
Nature Biotechnology
|
May 10, 2023
Pangenome graph construction from genome alignments with Minigraph-Cactus
Glenn Hickey, Jean Monlong, Jana Ebler, et al.
Biorxiv : the Preprint Server for Biology
|
October 28, 2024
Efficient indexing and querying of annotations in a pangenome graph
Adam M Novak, Dickson Chung, Glenn Hickey, et al.
Genome Biology
|
February 14, 2020
Genotyping structural variants in pangenome graphs using the vg toolkit
Glenn Hickey, David Heller, Jean Monlong, et al.
Nature Communications
|
October 26, 2019
Genome-wide microhomologies enable precise template-free editing of biologically relevant deletion mutations
Janin Grajcarek, Jean Monlong, Yoko Nishinaka-Arai, et al.
Nature Methods
|
September 11, 2024
Personalized pangenome references
Jouni Sirén, Parsa Eskandar, Matteo Tommaso Ungaro, et al.
Page
of 5