Chong-Jian Chen - JoVE Visualize

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Genome Biology|December 2, 2015

HiC-Pro: an optimized and flexible pipeline for Hi-C data processingNicolas Servant, Nelle Varoquaux, Bryan R Lajoie, et al.

Bioinformatics (Oxford, England)|October 10, 2012

ncPRO-seq: a tool for annotation and profiling of ncRNAs in sRNA-seq dataChong-Jian Chen, Nicolas Servant, Joern Toedling, et al.

Nature|July 21, 2016

Structural organization of the inactive X chromosome in the mouseLuca Giorgetti, Bryan R Lajoie, Ava C Carter, et al.

Elife|February 3, 2016

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activationKatia Ancelin, Laurène Syx, Maud Borensztein, et al.

Nature Structural & Molecular Biology|January 31, 2017

Xist-dependent imprinted X inactivation and the early developmental consequences of its failureMaud Borensztein, Laurène Syx, Katia Ancelin, et al.

Genome Research|June 9, 2019

Kinetics of <i>Xist</i>-induced gene silencing can be predicted from combinations of epigenetic and genomic featuresLisa Barros de Andrade E Sousa, Iris Jonkers, Laurène Syx, et al.

Nature Communications|November 5, 2017

Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell massMaud Borensztein, Ikuhiro Okamoto, Laurène Syx, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 12, 2018

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencingHong Qi, Zhao-Ling Xuan, Yang Du, et al.

Scientific Reports|November 5, 2015

Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number VariationHan Zhang, Yang-Yu Zhao, Jing Song, et al.

Cancer Medicine|September 24, 2020

Characteristics and prognostic significance of genetic mutations in acute myeloid leukemia based on a targeted next-generation sequencing techniqueRui-Qi Wang, Chong-Jian Chen, Yu Jing, et al.

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Showing results (11-20 of 21) with videos related to

Sort By:

Pageof 3

Genome Biology|December 2, 2015

HiC-Pro: an optimized and flexible pipeline for Hi-C data processingNicolas Servant, Nelle Varoquaux, Bryan R Lajoie, et al.

Bioinformatics (Oxford, England)|October 10, 2012

ncPRO-seq: a tool for annotation and profiling of ncRNAs in sRNA-seq dataChong-Jian Chen, Nicolas Servant, Joern Toedling, et al.

Nature|July 21, 2016

Structural organization of the inactive X chromosome in the mouseLuca Giorgetti, Bryan R Lajoie, Ava C Carter, et al.

Elife|February 3, 2016

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activationKatia Ancelin, Laurène Syx, Maud Borensztein, et al.

Nature Structural & Molecular Biology|January 31, 2017

Xist-dependent imprinted X inactivation and the early developmental consequences of its failureMaud Borensztein, Laurène Syx, Katia Ancelin, et al.

Genome Research|June 9, 2019

Kinetics of <i>Xist</i>-induced gene silencing can be predicted from combinations of epigenetic and genomic featuresLisa Barros de Andrade E Sousa, Iris Jonkers, Laurène Syx, et al.

Nature Communications|November 5, 2017

Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell massMaud Borensztein, Ikuhiro Okamoto, Laurène Syx, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 12, 2018

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencingHong Qi, Zhao-Ling Xuan, Yang Du, et al.

Scientific Reports|November 5, 2015

Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number VariationHan Zhang, Yang-Yu Zhao, Jing Song, et al.

Cancer Medicine|September 24, 2020

Characteristics and prognostic significance of genetic mutations in acute myeloid leukemia based on a targeted next-generation sequencing techniqueRui-Qi Wang, Chong-Jian Chen, Yu Jing, et al.

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