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BMC Genomics
|
October 1, 2014
Open-access synthetic spike-in mRNA-seq data for cancer gene fusions
Waibhav D Tembe, Stephanie J K Pond, Christophe Legendre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 20, 2010
B-cell activating factor and v-Myc myelocytomatosis viral oncogene homolog (c-Myc) influence progression of chronic lymphocytic leukemia
Weizhou Zhang, Arnon P Kater, George F Widhopf, et al.
Bioinformatics (Oxford, England)
|
October 11, 2018
Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data
Tamsen Dunn, Gwenn Berry, Dorothea Emig-Agius, et al.
Bioinformatics (Oxford, England)
|
June 6, 2013
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
Come Raczy, Roman Petrovski, Christopher T Saunders, et al.
Genome Research
|
December 2, 2016
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree
Michael A Eberle, Epameinondas Fritzilas, Peter Krusche, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 17, 2025
Noninvasive Assessment of β-Secretase Activity Through Click Chemistry-Mediated Enrichment of Neuronal Extracellular Vesicles to Detect Alzheimer's Disease
Hyoyong Kim, Junseok Lee, Audrey Qian, et al.
Veterinary and Comparative Oncology
|
December 6, 2023
Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential
Sharadha Sakthikumar, Manisha Warrier, Derick Whitley, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 25, 2017
Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer
Filip Janku, Shile Zhang, Jill Waters, et al.
Nucleic Acids Research
|
October 11, 2005
The subsystems approach to genome annotation and its use in the project to annotate 1000 genomes
Ross Overbeek, Tadhg Begley, Ralph M Butler, et al.
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Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
BMC Genomics
|
October 1, 2014
Open-access synthetic spike-in mRNA-seq data for cancer gene fusions
Waibhav D Tembe, Stephanie J K Pond, Christophe Legendre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 20, 2010
B-cell activating factor and v-Myc myelocytomatosis viral oncogene homolog (c-Myc) influence progression of chronic lymphocytic leukemia
Weizhou Zhang, Arnon P Kater, George F Widhopf, et al.
Bioinformatics (Oxford, England)
|
October 11, 2018
Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data
Tamsen Dunn, Gwenn Berry, Dorothea Emig-Agius, et al.
Bioinformatics (Oxford, England)
|
June 6, 2013
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
Come Raczy, Roman Petrovski, Christopher T Saunders, et al.
Genome Research
|
December 2, 2016
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree
Michael A Eberle, Epameinondas Fritzilas, Peter Krusche, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 17, 2025
Noninvasive Assessment of β-Secretase Activity Through Click Chemistry-Mediated Enrichment of Neuronal Extracellular Vesicles to Detect Alzheimer's Disease
Hyoyong Kim, Junseok Lee, Audrey Qian, et al.
Veterinary and Comparative Oncology
|
December 6, 2023
Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential
Sharadha Sakthikumar, Manisha Warrier, Derick Whitley, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 25, 2017
Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer
Filip Janku, Shile Zhang, Jill Waters, et al.
Nucleic Acids Research
|
October 11, 2005
The subsystems approach to genome annotation and its use in the project to annotate 1000 genomes
Ross Overbeek, Tadhg Begley, Ralph M Butler, et al.
Page
of 2