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John V Pearson

Showing results (11-20 of 114) with videos related to

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Gigascience|April 4, 2026
Cancer genome standards for long-read sequencing using cancer cell line mixturesJia Zhang, Ho Yi Wong, Lingchen Liu, et al.
Journal of Proteome Research|March 12, 2015
PGTools: A Software Suite for Proteogenomic Data Analysis and VisualizationShivashankar H Nagaraj, Nicola Waddell, Anil K Madugundu, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Human Mutation|February 18, 2021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a modelAimee L Davidson, Conrad Leonard, Lambros T Koufariotis, et al.
Human Mutation|September 12, 2022
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertionsAimee L Davidson, Olga Kondrashova, Conrad Leonard, et al.
Pigment Cell & Melanoma Research|December 27, 2016
Mutation load in melanoma is affected by MC1R genotypePeter A Johansson, Antonia L Pritchard, Ann-Marie Patch, et al.
Cancers|April 30, 2021
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer DevelopmentOlga Kondrashova, Jannah Shamsani, Tracy A O'Mara, et al.
Neuro-Oncology|February 9, 2023
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screeningMarija Kojic, Mellissa K Maybury, Nicola Waddell, et al.
Scientific Reports|January 30, 2021
Verifying explainability of a deep learning tissue classifier trained on RNA-seq dataMelvyn Yap, Rebecca L Johnston, Helena Foley, et al.
BMC Cancer|June 5, 2017
Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesotheliomaSophie Sneddon, Ann-Marie Patch, Ian M Dick, et al.
Pageof 12

Showing results (11-20 of 114) with videos related to

Sort By:
Pageof 12
Gigascience|April 4, 2026
Cancer genome standards for long-read sequencing using cancer cell line mixturesJia Zhang, Ho Yi Wong, Lingchen Liu, et al.
Journal of Proteome Research|March 12, 2015
PGTools: A Software Suite for Proteogenomic Data Analysis and VisualizationShivashankar H Nagaraj, Nicola Waddell, Anil K Madugundu, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Human Mutation|February 18, 2021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a modelAimee L Davidson, Conrad Leonard, Lambros T Koufariotis, et al.
Human Mutation|September 12, 2022
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertionsAimee L Davidson, Olga Kondrashova, Conrad Leonard, et al.
Pigment Cell & Melanoma Research|December 27, 2016
Mutation load in melanoma is affected by MC1R genotypePeter A Johansson, Antonia L Pritchard, Ann-Marie Patch, et al.
Cancers|April 30, 2021
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer DevelopmentOlga Kondrashova, Jannah Shamsani, Tracy A O'Mara, et al.
Neuro-Oncology|February 9, 2023
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screeningMarija Kojic, Mellissa K Maybury, Nicola Waddell, et al.
Scientific Reports|January 30, 2021
Verifying explainability of a deep learning tissue classifier trained on RNA-seq dataMelvyn Yap, Rebecca L Johnston, Helena Foley, et al.
BMC Cancer|June 5, 2017
Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesotheliomaSophie Sneddon, Ann-Marie Patch, Ian M Dick, et al.
Pageof 12