Search research articles
Contact Us
Filters
Showing results (1-10 of 136) with videos related to
Page
of 14
Sort By:
Bioinformatics (Oxford, England)
|
September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordance
Niko Popitsch, , Anna Schuh, et al.
Nucleic Acids Research
|
March 2, 2022
GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing data
Edoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
Bioinformatics (Oxford, England)
|
June 3, 2017
Hierarchical probabilistic models for multiple gene/variant associations based on next-generation sequencing data
Dimitrios V Vavoulis, Jenny C Taylor, Anna Schuh
Journal of Medical Genetics
|
December 11, 2024
Hiding in plain sight: a partial deletion of <i>BRCA1</i> exon 7 undetectable by MLPA is a Nepali founder variant
Virginia Clowes, Jenny C Taylor, Alistair T Pagnamenta
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 16, 2018
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
Katharina Schwarze, James Buchanan, Jenny C Taylor, et al.
Bioinformatics (Oxford, England)
|
July 30, 2020
A statistical approach for tracking clonal dynamics in cancer using longitudinal next-generation sequencing data
Dimitrios V Vavoulis, Anthony Cutts, Jenny C Taylor, et al.
BMC Genomics
|
February 3, 2018
A high throughput screen for active human transposable elements
Erika M Kvikstad, Paolo Piazza, Jenny C Taylor, et al.
Molecular Immunology
|
October 19, 2004
Cytoplasmic domains of the transporter associated with antigen processing and P-glycoprotein interact with subunits of the proteasome
Gail S Begley, Andrea R Horvath, Jenny C Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2022
Can polygenic risk scores contribute to cost-effective cancer screening? A systematic review
Padraig Dixon, Edna Keeney, Jenny C Taylor, et al.
European Journal of Human Genetics : EJHG
|
June 1, 2026
The cost and cost-effectiveness of whole-exome and whole-genome sequencing: a systematic literature review
Frederick McElwee, Sally L Sansom, James Buchanan, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 136) with videos related to
Sort By:
Page
of 14
Bioinformatics (Oxford, England)
|
September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordance
Niko Popitsch, , Anna Schuh, et al.
Nucleic Acids Research
|
March 2, 2022
GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing data
Edoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
Bioinformatics (Oxford, England)
|
June 3, 2017
Hierarchical probabilistic models for multiple gene/variant associations based on next-generation sequencing data
Dimitrios V Vavoulis, Jenny C Taylor, Anna Schuh
Journal of Medical Genetics
|
December 11, 2024
Hiding in plain sight: a partial deletion of <i>BRCA1</i> exon 7 undetectable by MLPA is a Nepali founder variant
Virginia Clowes, Jenny C Taylor, Alistair T Pagnamenta
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 16, 2018
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
Katharina Schwarze, James Buchanan, Jenny C Taylor, et al.
Bioinformatics (Oxford, England)
|
July 30, 2020
A statistical approach for tracking clonal dynamics in cancer using longitudinal next-generation sequencing data
Dimitrios V Vavoulis, Anthony Cutts, Jenny C Taylor, et al.
BMC Genomics
|
February 3, 2018
A high throughput screen for active human transposable elements
Erika M Kvikstad, Paolo Piazza, Jenny C Taylor, et al.
Molecular Immunology
|
October 19, 2004
Cytoplasmic domains of the transporter associated with antigen processing and P-glycoprotein interact with subunits of the proteasome
Gail S Begley, Andrea R Horvath, Jenny C Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2022
Can polygenic risk scores contribute to cost-effective cancer screening? A systematic review
Padraig Dixon, Edna Keeney, Jenny C Taylor, et al.
European Journal of Human Genetics : EJHG
|
June 1, 2026
The cost and cost-effectiveness of whole-exome and whole-genome sequencing: a systematic literature review
Frederick McElwee, Sally L Sansom, James Buchanan, et al.
Page
of 14