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JNCI Cancer Spectrum
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July 31, 2019
Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers
Shawn Yost, Elise Ruark, Ludmil B Alexandrov, et al.
Wellcome Open Research
|
December 4, 2018
ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series
Elise Ruark, Esty Holt, Anthony Renwick, et al.
Wellcome Open Research
|
June 9, 2018
CoverView: a sequence quality evaluation tool for next generation sequencing data
Márton Münz, Shazia Mahamdallie, Shawn Yost, et al.
Wellcome Open Research
|
July 12, 2018
The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance
Shazia Mahamdallie, Elise Ruark, Shawn Yost, et al.
Wellcome Open Research
|
June 21, 2017
The ICR96 exon CNV validation series: a resource for orthogonal assessment of exon CNV calling in NGS data
Shazia Mahamdallie, Elise Ruark, Shawn Yost, et al.
Plos One
|
November 12, 2015
Mutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors
Lei Bao, Karen Messer, Richard Schwab, et al.
JAMA Network Open
|
May 25, 2019
Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer
Zoe Kemp, Alice Turnbull, Shawn Yost, et al.
Nature Communications
|
January 23, 2015
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Kevin Litchfield, Brenda Summersgill, Shawn Yost, et al.
Genome Medicine
|
June 20, 2014
Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin
Hakan Alakus, Michele L Babicky, Pradipta Ghosh, et al.
American Journal of Human Genetics
|
May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
Katrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
JNCI Cancer Spectrum
|
July 31, 2019
Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers
Shawn Yost, Elise Ruark, Ludmil B Alexandrov, et al.
Wellcome Open Research
|
December 4, 2018
ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series
Elise Ruark, Esty Holt, Anthony Renwick, et al.
Wellcome Open Research
|
June 9, 2018
CoverView: a sequence quality evaluation tool for next generation sequencing data
Márton Münz, Shazia Mahamdallie, Shawn Yost, et al.
Wellcome Open Research
|
July 12, 2018
The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance
Shazia Mahamdallie, Elise Ruark, Shawn Yost, et al.
Wellcome Open Research
|
June 21, 2017
The ICR96 exon CNV validation series: a resource for orthogonal assessment of exon CNV calling in NGS data
Shazia Mahamdallie, Elise Ruark, Shawn Yost, et al.
Plos One
|
November 12, 2015
Mutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors
Lei Bao, Karen Messer, Richard Schwab, et al.
JAMA Network Open
|
May 25, 2019
Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer
Zoe Kemp, Alice Turnbull, Shawn Yost, et al.
Nature Communications
|
January 23, 2015
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Kevin Litchfield, Brenda Summersgill, Shawn Yost, et al.
Genome Medicine
|
June 20, 2014
Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin
Hakan Alakus, Michele L Babicky, Pradipta Ghosh, et al.
American Journal of Human Genetics
|
May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
Katrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
Page
of 2