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Leming Shi

Showing results (211-220 of 227) with videos related to

Pageof 23
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Nature Biotechnology|August 25, 2014
The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundanceCharles Wang, Binsheng Gong, Pierre R Bushel, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
BMC Bioinformatics|September 20, 2008
The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed genes in microarray studiesLeming Shi, Wendell D Jones, Roderick V Jensen, et al.
Nature Biotechnology|September 7, 2023
Multi-omics data integration using ratio-based quantitative profiling with Quartet reference materialsYuanting Zheng, Yaqing Liu, Jingcheng Yang, et al.
Nature|October 16, 2015
Telomerase activation by genomic rearrangements in high-risk neuroblastomaMartin Peifer, Falk Hertwig, Frederik Roels, et al.
Nature Methods|September 24, 2005
The External RNA Controls Consortium: a progress reportShawn C Baker, Steven R Bauer, Richard P Beyer, et al.
Scientific Reports|March 26, 2024
Extend the benchmarking indel set by manual review using the individual cell line sequencing data from the Sequencing Quality Control 2 (SEQC2) projectBinsheng Gong, Dan Li, Yifan Zhang, et al.
Genome Biology|April 17, 2021
A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequencyWendell Jones, Binsheng Gong, Natalia Novoradovskaya, et al.
Nature Biotechnology|September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencingLi Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Genome Biology|June 26, 2015
Comparison of RNA-seq and microarray-based models for clinical endpoint predictionWenqian Zhang, Ying Yu, Falk Hertwig, et al.
Pageof 23

Showing results (211-220 of 227) with videos related to

Sort By:
Pageof 23
Nature Biotechnology|August 25, 2014
The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundanceCharles Wang, Binsheng Gong, Pierre R Bushel, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
BMC Bioinformatics|September 20, 2008
The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed genes in microarray studiesLeming Shi, Wendell D Jones, Roderick V Jensen, et al.
Nature Biotechnology|September 7, 2023
Multi-omics data integration using ratio-based quantitative profiling with Quartet reference materialsYuanting Zheng, Yaqing Liu, Jingcheng Yang, et al.
Nature|October 16, 2015
Telomerase activation by genomic rearrangements in high-risk neuroblastomaMartin Peifer, Falk Hertwig, Frederik Roels, et al.
Nature Methods|September 24, 2005
The External RNA Controls Consortium: a progress reportShawn C Baker, Steven R Bauer, Richard P Beyer, et al.
Scientific Reports|March 26, 2024
Extend the benchmarking indel set by manual review using the individual cell line sequencing data from the Sequencing Quality Control 2 (SEQC2) projectBinsheng Gong, Dan Li, Yifan Zhang, et al.
Genome Biology|April 17, 2021
A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequencyWendell Jones, Binsheng Gong, Natalia Novoradovskaya, et al.
Nature Biotechnology|September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencingLi Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Genome Biology|June 26, 2015
Comparison of RNA-seq and microarray-based models for clinical endpoint predictionWenqian Zhang, Ying Yu, Falk Hertwig, et al.
Pageof 23