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The Journal of Molecular Diagnostics : JMD
|
December 15, 2019
Concordance of Genomic Alterations by Next-Generation Sequencing in Tumor Tissue versus Cell-Free DNA in Stage I-IV Non-Small Cell Lung Cancer
John Jiang, Hans-Peter Adams, Lijing Yao, et al.
Genome Biology
|
September 19, 2015
An ensemble approach to accurately detect somatic mutations using SomaticSeq
Li Tai Fang, Pegah Tootoonchi Afshar, Aparna Chhibber, et al.
Scientific Data
|
November 10, 2021
Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
Yongmei Zhao, Li Tai Fang, Tsai-Wei Shen, et al.
Genome Biology
|
December 13, 2022
Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
Keyur Talsania, Tsai-Wei Shen, Xiongfong Chen, et al.
Cell Genomics
|
June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature Biotechnology
|
September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Li Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Nature Biotechnology
|
September 10, 2021
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing
Wenming Xiao, Luyao Ren, Zhong Chen, et al.
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Showing results (21-30 of 27) with videos related to
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Page
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You have reached the last page of results.
This site can display upto 27 results.
The Journal of Molecular Diagnostics : JMD
|
December 15, 2019
Concordance of Genomic Alterations by Next-Generation Sequencing in Tumor Tissue versus Cell-Free DNA in Stage I-IV Non-Small Cell Lung Cancer
John Jiang, Hans-Peter Adams, Lijing Yao, et al.
Genome Biology
|
September 19, 2015
An ensemble approach to accurately detect somatic mutations using SomaticSeq
Li Tai Fang, Pegah Tootoonchi Afshar, Aparna Chhibber, et al.
Scientific Data
|
November 10, 2021
Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
Yongmei Zhao, Li Tai Fang, Tsai-Wei Shen, et al.
Genome Biology
|
December 13, 2022
Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
Keyur Talsania, Tsai-Wei Shen, Xiongfong Chen, et al.
Cell Genomics
|
June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature Biotechnology
|
September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Li Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Nature Biotechnology
|
September 10, 2021
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing
Wenming Xiao, Luyao Ren, Zhong Chen, et al.
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of 3