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Genome Research
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February 13, 2010
Accurate detection and genotyping of SNPs utilizing population sequencing data
Vikas Bansal, Olivier Harismendy, Ryan Tewhey, et al.
Bioinformatics (Oxford, England)
|
July 13, 2014
Network-based analysis identifies epigenetic biomarkers of esophageal squamous cell carcinoma progression
Chun-Pei Cheng, I-Ying Kuo, Hakan Alakus, et al.
Genome Research
|
February 14, 2004
Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional
Kelly A Frazer, Heng Tao, Kazutoyo Osoegawa, et al.
BMC Bioinformatics
|
June 3, 2014
Effective filtering strategies to improve data quality from population-based whole exome sequencing studies
Andrew R Carson, Erin N Smith, Hiroko Matsui, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Characterization of shared and ancestry-specific signals driving complex traits using multi-ancestry fine-mapping
Tara Mirmira, Nichole Ma, Jonathan Margoliash, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 31, 2014
Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD
Peter J Shepard, Bruce A Barshop, Matthias R Baumgartner, et al.
Plos Computational Biology
|
February 28, 2022
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, et al.
Journal of Translational Medicine
|
April 19, 2015
BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma
Hakan Alakus, Shawn E Yost, Brian Woo, et al.
Science (New York, N.Y.)
|
February 19, 2005
Whole-genome patterns of common DNA variation in three human populations
David A Hinds, Laura L Stuve, Geoffrey B Nilsen, et al.
Nature Genetics
|
February 22, 2005
Fine-scale recombination patterns differ between chimpanzees and humans
Susan E Ptak, David A Hinds, Kathrin Koehler, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 151) with videos related to
Sort By:
Page
of 16
Genome Research
|
February 13, 2010
Accurate detection and genotyping of SNPs utilizing population sequencing data
Vikas Bansal, Olivier Harismendy, Ryan Tewhey, et al.
Bioinformatics (Oxford, England)
|
July 13, 2014
Network-based analysis identifies epigenetic biomarkers of esophageal squamous cell carcinoma progression
Chun-Pei Cheng, I-Ying Kuo, Hakan Alakus, et al.
Genome Research
|
February 14, 2004
Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional
Kelly A Frazer, Heng Tao, Kazutoyo Osoegawa, et al.
BMC Bioinformatics
|
June 3, 2014
Effective filtering strategies to improve data quality from population-based whole exome sequencing studies
Andrew R Carson, Erin N Smith, Hiroko Matsui, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Characterization of shared and ancestry-specific signals driving complex traits using multi-ancestry fine-mapping
Tara Mirmira, Nichole Ma, Jonathan Margoliash, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 31, 2014
Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD
Peter J Shepard, Bruce A Barshop, Matthias R Baumgartner, et al.
Plos Computational Biology
|
February 28, 2022
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, et al.
Journal of Translational Medicine
|
April 19, 2015
BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma
Hakan Alakus, Shawn E Yost, Brian Woo, et al.
Science (New York, N.Y.)
|
February 19, 2005
Whole-genome patterns of common DNA variation in three human populations
David A Hinds, Laura L Stuve, Geoffrey B Nilsen, et al.
Nature Genetics
|
February 22, 2005
Fine-scale recombination patterns differ between chimpanzees and humans
Susan E Ptak, David A Hinds, Kathrin Koehler, et al.
Page
of 16