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Human Mutation
|
March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing
Zirui Dong, Lupin Jiang, Chuanchun Yang, et al.
Nucleic Acids Research
|
January 17, 2020
Haplotyping by CRISPR-mediated DNA circularization (CRISPR-hapC) broadens allele-specific gene editing
Jiaying Yu, Xi Xiang, Jinrong Huang, et al.
Human Mutation
|
June 28, 2013
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism
Marialuisa Quadri, Mingyan Fang, Marina Picillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2017
Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics
Zirui Dong, Huilin Wang, Haixiao Chen, et al.
Transboundary and Emerging Diseases
|
April 30, 2025
Tracing the Origin of Genotype II African Swine Fever Virus in China by Genomic Epidemiology Analysis
Yong Zhang, Qinghua Wang, Zhongyi Zhu, et al.
Nature Communications
|
May 29, 2021
Enhancing CRISPR-Cas9 gRNA efficiency prediction by data integration and deep learning
Xi Xiang, Giulia I Corsi, Christian Anthon, et al.
Gigascience
|
April 11, 2018
Genome-wide determination of on-target and off-target characteristics for RNA-guided DNA methylation by dCas9 methyltransferases
Lin Lin, Yong Liu, Fengping Xu, et al.
Nature Communications
|
July 13, 2022
Massively targeted evaluation of therapeutic CRISPR off-targets in cells
Xiaoguang Pan, Kunli Qu, Hao Yuan, et al.
BMC Biology
|
January 25, 2022
Genome-wide annotation of protein-coding genes in pig
Max Karlsson, Evelina Sjöstedt, Per Oksvold, et al.
Stem Cell Reports
|
February 21, 2017
Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B
Yu Zhang, Benjamin Schmid, Nanett K Nikolaisen, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
Human Mutation
|
March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing
Zirui Dong, Lupin Jiang, Chuanchun Yang, et al.
Nucleic Acids Research
|
January 17, 2020
Haplotyping by CRISPR-mediated DNA circularization (CRISPR-hapC) broadens allele-specific gene editing
Jiaying Yu, Xi Xiang, Jinrong Huang, et al.
Human Mutation
|
June 28, 2013
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism
Marialuisa Quadri, Mingyan Fang, Marina Picillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2017
Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics
Zirui Dong, Huilin Wang, Haixiao Chen, et al.
Transboundary and Emerging Diseases
|
April 30, 2025
Tracing the Origin of Genotype II African Swine Fever Virus in China by Genomic Epidemiology Analysis
Yong Zhang, Qinghua Wang, Zhongyi Zhu, et al.
Nature Communications
|
May 29, 2021
Enhancing CRISPR-Cas9 gRNA efficiency prediction by data integration and deep learning
Xi Xiang, Giulia I Corsi, Christian Anthon, et al.
Gigascience
|
April 11, 2018
Genome-wide determination of on-target and off-target characteristics for RNA-guided DNA methylation by dCas9 methyltransferases
Lin Lin, Yong Liu, Fengping Xu, et al.
Nature Communications
|
July 13, 2022
Massively targeted evaluation of therapeutic CRISPR off-targets in cells
Xiaoguang Pan, Kunli Qu, Hao Yuan, et al.
BMC Biology
|
January 25, 2022
Genome-wide annotation of protein-coding genes in pig
Max Karlsson, Evelina Sjöstedt, Per Oksvold, et al.
Stem Cell Reports
|
February 21, 2017
Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B
Yu Zhang, Benjamin Schmid, Nanett K Nikolaisen, et al.
Page
of 5