Sally M. Harrison

Leeds, ENG LS29NL, United Kingdom

Last Updated: 09/26/2026

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Found 14 publications

How to analyse the spatiotemporal tumour samples needed to investigate cancer evolution: A case study using paired primary and recurrent glioblastoma.

How to analyse the spatiotemporal tumour samples needed to investigate cancer evolution: A case study using paired primary and recurrent glioblastoma.

Journal: International journal of cancer

Published: September 07, 2017

Novel avian paramyxovirus isolated from gulls in Caspian seashore in Kazakhstan.

Novel avian paramyxovirus isolated from gulls in Caspian seashore in Kazakhstan.

Journal: PloS one

Published: August 10, 2017

Upregulated WEE1 protects endothelial cells of colorectal cancer liver metastases.

Upregulated WEE1 protects endothelial cells of colorectal cancer liver metastases.

Journal: Oncotarget

Published: October 02, 2016

m6aViewer: software for the detection, analysis, and visualization of N6-methyladenosine peaks from m6A-seq/ME-RIP sequencing data.

m6aViewer: software for the detection, analysis, and visualization of N6-methyladenosine peaks from m6A-seq/ME-RIP sequencing data.

Journal: RNA (New York, N.Y.)

Published: July 06, 2016

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome.

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome.

Journal: PloS one

Published: March 24, 2016

Exploring the surfaceome of Ewing sarcoma identifies a new and unique therapeutic target.

Exploring the surfaceome of Ewing sarcoma identifies a new and unique therapeutic target.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 17, 2016

Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia.

Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia.

Journal: Journal of medical genetics

Published: November 04, 2015

Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping.

Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping.

Journal: BMC medical genetics

Published: September 16, 2015

OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization.

OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization.

Journal: Bioinformatics (Oxford, England)

Published: May 19, 2015

Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data.

Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data.

Journal: Human mutation

Published: March 30, 2015

Detection of somatic mutations in tumors using unaligned clonal sequencing data.

Detection of somatic mutations in tumors using unaligned clonal sequencing data.

Journal: Laboratory investigation; a journal of technical methods and pathology

Published: March 19, 2014

Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome.

Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome.

Journal: American journal of medical genetics. Part A

Published: March 18, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026