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E Rodin

Showing results (111-120 of 122) with videos related to

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Nature Biotechnology|January 8, 2020
Accurate detection of mosaic variants in sequencing data without matched controlsYanmei Dou, Minseok Kwon, Rachel E Rodin, et al.
Nature Neuroscience|January 12, 2021
Large mosaic copy number variations confer autism riskMaxwell A Sherman, Rachel E Rodin, Giulio Genovese, et al.
BMC Medical Genomics|February 13, 2021
MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutationsRyan N Doan, Michael B Miller, Sonia N Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2020
Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brainAugust Yue Huang, Pengpeng Li, Rachel E Rodin, et al.
Nature Genetics|March 20, 2019
Linked-read analysis identifies mutations in single-cell DNA-sequencing dataCraig L Bohrson, Alison R Barton, Michael A Lodato, et al.
Nature Neuroscience|March 23, 2021
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Nature Neuroscience|January 12, 2021
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Nature Neuroscience|August 29, 2023
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Science (New York, N.Y.)|December 9, 2017
Aging and neurodegeneration are associated with increased mutations in single human neuronsMichael A Lodato, Rachel E Rodin, Craig L Bohrson, et al.
Genome Research|June 21, 2017
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor <i>DONSON</i> as the cause of microcephaly-micromelia syndromeGilad D Evrony, Dwight R Cordero, Jun Shen, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Nature Biotechnology|January 8, 2020
Accurate detection of mosaic variants in sequencing data without matched controlsYanmei Dou, Minseok Kwon, Rachel E Rodin, et al.
Nature Neuroscience|January 12, 2021
Large mosaic copy number variations confer autism riskMaxwell A Sherman, Rachel E Rodin, Giulio Genovese, et al.
BMC Medical Genomics|February 13, 2021
MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutationsRyan N Doan, Michael B Miller, Sonia N Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2020
Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brainAugust Yue Huang, Pengpeng Li, Rachel E Rodin, et al.
Nature Genetics|March 20, 2019
Linked-read analysis identifies mutations in single-cell DNA-sequencing dataCraig L Bohrson, Alison R Barton, Michael A Lodato, et al.
Nature Neuroscience|March 23, 2021
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Nature Neuroscience|January 12, 2021
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Nature Neuroscience|August 29, 2023
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Science (New York, N.Y.)|December 9, 2017
Aging and neurodegeneration are associated with increased mutations in single human neuronsMichael A Lodato, Rachel E Rodin, Craig L Bohrson, et al.
Genome Research|June 21, 2017
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor <i>DONSON</i> as the cause of microcephaly-micromelia syndromeGilad D Evrony, Dwight R Cordero, Jun Shen, et al.
Pageof 13