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Hanlee P Ji

Showing results (11-20 of 106) with videos related to

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Genome Medicine|October 29, 2015
The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associationsHoJoon Lee, Jennifer Palm, Susan M Grimes, et al.
BMC Biotechnology|December 16, 2011
Targeted sequencing library preparation by genomic DNA circularizationSamuel Myllykangas, Georges Natsoulis, John M Bell, et al.
Analytical Chemistry|February 4, 2014
High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCRLaura Miotke, Billy T Lau, Rowza T Rumma, et al.
Journal of Data Mining in Genomics & Proteomics|February 11, 2014
Identification of Insertion Deletion Mutations from Deep Targeted ResequencingGeorges Natsoulis, Nancy Zhang, Katrina Welch, et al.
NAR Genomics and Bioinformatics|March 3, 2020
CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index countingHoJoon Lee, Howard Y Chang, Seung Woo Cho, et al.
Analytical Chemistry|February 13, 2015
Correction to High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCRLaura Miotke, Billy T Lau, Rowza T Rumma, et al.
JCO Precision Oncology|September 11, 2020
Precision Oncology Strategy in Trastuzumab-Resistant Human Epidermal Growth Factor Receptor 2-Positive Colon Cancer: Case Report of Durable Response to Ado-Trastuzumab EmtansineDerrick S Haslem, Hanlee P Ji, James M Ford, et al.
BMC Research Notes|May 25, 2013
RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencingAnna Cushing, Patrick Flaherty, Erik Hopmans, et al.
Genome Biology|December 13, 2019
scPred: accurate supervised method for cell-type classification from single-cell RNA-seq dataJose Alquicira-Hernandez, Anuja Sathe, Hanlee P Ji, et al.
NAR Cancer|December 21, 2020
Unique <i>k</i>-mer sequences for validating cancer-related substitution, insertion and deletion mutationsHoJoon Lee, Ahmed Shuaibi, John M Bell, et al.
Pageof 11

Showing results (11-20 of 106) with videos related to

Sort By:
Pageof 11
Genome Medicine|October 29, 2015
The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associationsHoJoon Lee, Jennifer Palm, Susan M Grimes, et al.
BMC Biotechnology|December 16, 2011
Targeted sequencing library preparation by genomic DNA circularizationSamuel Myllykangas, Georges Natsoulis, John M Bell, et al.
Analytical Chemistry|February 4, 2014
High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCRLaura Miotke, Billy T Lau, Rowza T Rumma, et al.
Journal of Data Mining in Genomics & Proteomics|February 11, 2014
Identification of Insertion Deletion Mutations from Deep Targeted ResequencingGeorges Natsoulis, Nancy Zhang, Katrina Welch, et al.
NAR Genomics and Bioinformatics|March 3, 2020
CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index countingHoJoon Lee, Howard Y Chang, Seung Woo Cho, et al.
Analytical Chemistry|February 13, 2015
Correction to High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCRLaura Miotke, Billy T Lau, Rowza T Rumma, et al.
JCO Precision Oncology|September 11, 2020
Precision Oncology Strategy in Trastuzumab-Resistant Human Epidermal Growth Factor Receptor 2-Positive Colon Cancer: Case Report of Durable Response to Ado-Trastuzumab EmtansineDerrick S Haslem, Hanlee P Ji, James M Ford, et al.
BMC Research Notes|May 25, 2013
RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencingAnna Cushing, Patrick Flaherty, Erik Hopmans, et al.
Genome Biology|December 13, 2019
scPred: accurate supervised method for cell-type classification from single-cell RNA-seq dataJose Alquicira-Hernandez, Anuja Sathe, Hanlee P Ji, et al.
NAR Cancer|December 21, 2020
Unique <i>k</i>-mer sequences for validating cancer-related substitution, insertion and deletion mutationsHoJoon Lee, Ahmed Shuaibi, John M Bell, et al.
Pageof 11