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Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Robust footprinting with sample-specific Tn5 bias correction for bulk and single cell ATAC-seq
Yuxuan Lin, Hanzhi Wang, Parker C Wilson, et al.
Biometrics
|
April 1, 2018
Sensitivity analysis and power for instrumental variable studies
Xuran Wang, Yang Jiang, Nancy R Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 31, 2016
Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing
Yuchao Jiang, Yu Qiu, Andy J Minn, et al.
Nature Communications
|
June 9, 2026
Robust footprinting with sample-specific Tn5 bias correction for bulk and single cell ATAC-seq
Yuxuan Lin, Hanzhi Wang, Parker C Wilson, et al.
Nature Communications
|
January 24, 2019
Bulk tissue cell type deconvolution with multi-subject single-cell expression reference
Xuran Wang, Jihwan Park, Katalin Susztak, et al.
Bioinformatics (Oxford, England)
|
February 8, 2018
Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny
Eugene Urrutia, Hao Chen, Zilu Zhou, et al.
NPJ Breast Cancer
|
November 28, 2017
Functional germline variants as potential co-oncogenes
Divyansh Agarwal, Christoph Nowak, Nancy R Zhang, et al.
Nucleic Acids Research
|
January 26, 2015
CODEX: a normalization and copy number variation detection method for whole exome sequencing
Yuchao Jiang, Derek A Oldridge, Sharon J Diskin, et al.
Biometrika
|
July 24, 2012
Detecting simultaneous changepoints in multiple sequences
Nancy R Zhang, David O Siegmund, Hanlee Ji, et al.
Nucleic Acids Research
|
October 17, 2017
Accounting for technical noise in differential expression analysis of single-cell RNA sequencing data
Cheng Jia, Yu Hu, Derek Kelly, et al.
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of 8
Search research articles
Search
Showing results (11-20 of 78) with videos related to
Sort By:
Page
of 8
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Robust footprinting with sample-specific Tn5 bias correction for bulk and single cell ATAC-seq
Yuxuan Lin, Hanzhi Wang, Parker C Wilson, et al.
Biometrics
|
April 1, 2018
Sensitivity analysis and power for instrumental variable studies
Xuran Wang, Yang Jiang, Nancy R Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 31, 2016
Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing
Yuchao Jiang, Yu Qiu, Andy J Minn, et al.
Nature Communications
|
June 9, 2026
Robust footprinting with sample-specific Tn5 bias correction for bulk and single cell ATAC-seq
Yuxuan Lin, Hanzhi Wang, Parker C Wilson, et al.
Nature Communications
|
January 24, 2019
Bulk tissue cell type deconvolution with multi-subject single-cell expression reference
Xuran Wang, Jihwan Park, Katalin Susztak, et al.
Bioinformatics (Oxford, England)
|
February 8, 2018
Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny
Eugene Urrutia, Hao Chen, Zilu Zhou, et al.
NPJ Breast Cancer
|
November 28, 2017
Functional germline variants as potential co-oncogenes
Divyansh Agarwal, Christoph Nowak, Nancy R Zhang, et al.
Nucleic Acids Research
|
January 26, 2015
CODEX: a normalization and copy number variation detection method for whole exome sequencing
Yuchao Jiang, Derek A Oldridge, Sharon J Diskin, et al.
Biometrika
|
July 24, 2012
Detecting simultaneous changepoints in multiple sequences
Nancy R Zhang, David O Siegmund, Hanlee Ji, et al.
Nucleic Acids Research
|
October 17, 2017
Accounting for technical noise in differential expression analysis of single-cell RNA sequencing data
Cheng Jia, Yu Hu, Derek Kelly, et al.
Page
of 8