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2. AscatNgs: Identifying Somatically Acquired Copy‐Number Alterations from Whole‐Genome Sequencing Data. Issue 1 (8th December 2016)

3. CgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data. Issue 1 (8th December 2016)

4. CgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing. Issue 1 (17th December 2015)

5. Characterisation of the genomic landscape of CRLF2‐rearranged acute lymphoblastic leukemia. Issue 5 (18th January 2017)

7. COSMIC: somatic cancer genetics at high-resolution. Issue Volume 45:Issue D1(2017) (29th November 2016)

8. Fibroblastic growth factor receptor 1 amplification in osteosarcoma is associated with poor response to neo‐adjuvant chemotherapy. (27th May 2014)

9. Impact of socioeconomic status on disease phenotype, genomic landscape and outcomes in myelodysplastic syndromes. (20th April 2016)

10. Inherent Mosaicism and Extensive Mutation of Human Placentas. Issue 6 (June 2021)