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Genome Medicine
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October 29, 2015
The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associations
HoJoon Lee, Jennifer Palm, Susan M Grimes, et al.
BMC Biotechnology
|
December 16, 2011
Targeted sequencing library preparation by genomic DNA circularization
Samuel 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 PCR
Laura 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 Resequencing
Georges 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 counting
HoJoon 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 PCR
Laura 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 Emtansine
Derrick 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 resequencing
Anna 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 data
Jose 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 mutations
HoJoon Lee, Ahmed Shuaibi, John M Bell, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 106) with videos related to
Sort By:
Page
of 11
Genome Medicine
|
October 29, 2015
The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associations
HoJoon Lee, Jennifer Palm, Susan M Grimes, et al.
BMC Biotechnology
|
December 16, 2011
Targeted sequencing library preparation by genomic DNA circularization
Samuel 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 PCR
Laura 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 Resequencing
Georges 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 counting
HoJoon 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 PCR
Laura 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 Emtansine
Derrick 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 resequencing
Anna 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 data
Jose 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 mutations
HoJoon Lee, Ahmed Shuaibi, John M Bell, et al.
Page
of 11