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International Journal of Epidemiology
|
January 31, 2012
Epigenetics, epidemiology and mitochondrial DNA diseases
Patrick F Chinnery, Hannah R Elliott, Gavin Hudson, et al.
Thescientificworldjournal
|
March 12, 2013
Evaluation of allele frequency estimation using pooled sequencing data simulation
Yan Guo, David C Samuels, Jiang Li, et al.
BMC Genomics
|
November 27, 2012
The effect of strand bias in Illumina short-read sequencing data
Yan Guo, Jiang Li, Chung-I Li, et al.
Briefings in Functional Genomics
|
January 1, 2019
Corrigendum to: Single-nucleotide variants in human RNA: RNA editing and beyond
Yan Guo, Hui Yu, David C Samuels, et al.
Antimicrobial Agents and Chemotherapy
|
April 2, 2014
High proportion of heteroresistance in gyrA and gyrB in fluoroquinolone-resistant Mycobacterium tuberculosis clinical isolates
Brandon Eilertson, Fernanda Maruri, Amondrea Blackman, et al.
Briefings in Functional Genomics
|
October 13, 2018
Single-nucleotide variants in human RNA: RNA editing and beyond
Yan Guo, Hui Yu, David C Samuels, et al.
Trends in Genetics : TIG
|
August 11, 2020
Alternative Applications of Genotyping Array Data Using Multivariant Methods
David C Samuels, Jennifer E Below, Scott Ness, et al.
American Journal of Human Genetics
|
August 5, 2008
Pathogenic mitochondrial DNA mutations are common in the general population
Hannah R Elliott, David C Samuels, James A Eden, et al.
Journal of Opioid Management
|
January 23, 2023
Identifying problematic opioid use in electronic health record data: Are we looking in the right place?
Lori Schirle, Shinwho Kwun, Ashley Suh, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathy
Joanna L Elson, David C Samuels, Margaret A Johnson, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 163) with videos related to
Sort By:
Page
of 17
International Journal of Epidemiology
|
January 31, 2012
Epigenetics, epidemiology and mitochondrial DNA diseases
Patrick F Chinnery, Hannah R Elliott, Gavin Hudson, et al.
Thescientificworldjournal
|
March 12, 2013
Evaluation of allele frequency estimation using pooled sequencing data simulation
Yan Guo, David C Samuels, Jiang Li, et al.
BMC Genomics
|
November 27, 2012
The effect of strand bias in Illumina short-read sequencing data
Yan Guo, Jiang Li, Chung-I Li, et al.
Briefings in Functional Genomics
|
January 1, 2019
Corrigendum to: Single-nucleotide variants in human RNA: RNA editing and beyond
Yan Guo, Hui Yu, David C Samuels, et al.
Antimicrobial Agents and Chemotherapy
|
April 2, 2014
High proportion of heteroresistance in gyrA and gyrB in fluoroquinolone-resistant Mycobacterium tuberculosis clinical isolates
Brandon Eilertson, Fernanda Maruri, Amondrea Blackman, et al.
Briefings in Functional Genomics
|
October 13, 2018
Single-nucleotide variants in human RNA: RNA editing and beyond
Yan Guo, Hui Yu, David C Samuels, et al.
Trends in Genetics : TIG
|
August 11, 2020
Alternative Applications of Genotyping Array Data Using Multivariant Methods
David C Samuels, Jennifer E Below, Scott Ness, et al.
American Journal of Human Genetics
|
August 5, 2008
Pathogenic mitochondrial DNA mutations are common in the general population
Hannah R Elliott, David C Samuels, James A Eden, et al.
Journal of Opioid Management
|
January 23, 2023
Identifying problematic opioid use in electronic health record data: Are we looking in the right place?
Lori Schirle, Shinwho Kwun, Ashley Suh, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathy
Joanna L Elson, David C Samuels, Margaret A Johnson, et al.
Page
of 17