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John DiCarlo

Showing results (1-10 of 9) with videos related to

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BMC Genomics|December 7, 2014
Edge effects in calling variants from targeted amplicon sequencingRavi Vijaya Satya, John DiCarlo
BMC Bioinformatics|January 29, 2015
Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controlsFrank Reinecke, Ravi Vijaya Satya, John DiCarlo
BMC Genomics|April 1, 2014
Comparison of somatic mutation calling methods in amplicon and whole exome sequence dataHuilei Xu, John DiCarlo, Ravi Vijaya Satya, et al.
BMC Genomics|January 5, 2017
Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant callerChang Xu, Mohammad R Nezami Ranjbar, Zhong Wu, et al.
Scientific Reports|March 20, 2019
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMIQuan Peng, Chang Xu, Daniel Kim, et al.
Bioinformatics (Oxford, England)|September 8, 2018
smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiersChang Xu, Xiujing Gu, Raghavendra Padmanabhan, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 11, 2021
Development of a Smart Sleep Mask with Multiple SensorsBing Dang, John Dicarlo, Stanislav Lukashov, et al.
Bioinformatics (Oxford, England)|September 19, 2025
UMI-nea: a fast, robust tool for reference-free UMI deduplication and accurate quantificationJixin Deng, Jingxiao Zhang, Song Tian, et al.
JAMA|June 21, 2018
Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic CancerChunling Hu, Steven N Hart, Eric C Polley, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
BMC Genomics|December 7, 2014
Edge effects in calling variants from targeted amplicon sequencingRavi Vijaya Satya, John DiCarlo
BMC Bioinformatics|January 29, 2015
Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controlsFrank Reinecke, Ravi Vijaya Satya, John DiCarlo
BMC Genomics|April 1, 2014
Comparison of somatic mutation calling methods in amplicon and whole exome sequence dataHuilei Xu, John DiCarlo, Ravi Vijaya Satya, et al.
BMC Genomics|January 5, 2017
Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant callerChang Xu, Mohammad R Nezami Ranjbar, Zhong Wu, et al.
Scientific Reports|March 20, 2019
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMIQuan Peng, Chang Xu, Daniel Kim, et al.
Bioinformatics (Oxford, England)|September 8, 2018
smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiersChang Xu, Xiujing Gu, Raghavendra Padmanabhan, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 11, 2021
Development of a Smart Sleep Mask with Multiple SensorsBing Dang, John Dicarlo, Stanislav Lukashov, et al.
Bioinformatics (Oxford, England)|September 19, 2025
UMI-nea: a fast, robust tool for reference-free UMI deduplication and accurate quantificationJixin Deng, Jingxiao Zhang, Song Tian, et al.
JAMA|June 21, 2018
Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic CancerChunling Hu, Steven N Hart, Eric C Polley, et al.
Pageof 1