Showing results (1-10 of 28) with videos related to
Sort By:
Pageof 3
The American Journal of Pathology|April 15, 2014
Genomic aberrations of BRCA1-mutated fallopian tube carcinomasSally M Hunter, Georgina L Ryland, Phillip Moss, et al.The Journal of Molecular Diagnostics : JMD|July 26, 2024
Economic Impact of Whole Genome Sequencing and Whole Transcriptome Sequencing Versus Routine Diagnostic Molecular Testing to Stratify Patients with B-Cell Acute Lymphoblastic LeukemiaMartin Vu, Koen Degeling, Georgina L Ryland, et al.BMC Cancer|May 18, 2011
Analysis of the mitogen-activated protein kinase kinase 4 (MAP2K4) tumor suppressor gene in ovarian cancerSally J Davis, David Y H Choong, Manasa Ramakrishna, et al.Genome Biology|January 7, 2022
JAFFAL: detecting fusion genes with long-read transcriptome sequencingNadia M Davidson, Ying Chen, Teresa Sadras, et al.BMC Genomics|August 30, 2014
Inferring copy number and genotype in tumour exome dataKaushalya C Amarasinghe, Jason Li, Sally M Hunter, et al.Journal of Clinical Pathology|August 13, 2017
Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignanciesCostas K Yannakou, Kate Jones, Georgina L Ryland, et al.Genome Medicine|October 1, 2013
A simple consensus approach improves somatic mutation prediction accuracyDavid L Goode, Sally M Hunter, Maria A Doyle, et al.Journal of Clinical Pathology|May 16, 2018
Novel genomic findings in multiple myeloma identified through routine diagnostic sequencingGeorgina L Ryland, Kate Jones, Melody Chin, et al.The Journal of Pathology|October 26, 2012
RNF43 is a tumour suppressor gene mutated in mucinous tumours of the ovaryGeorgina L Ryland, Sally M Hunter, Maria A Doyle, et al.Bioinformatics (Oxford, England)|April 5, 2012
CONTRA: copy number analysis for targeted resequencingJason Li, Richard Lupat, Kaushalya C Amarasinghe, et al.Pageof 3