Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for Saturation Genome Editing and other Deep Mutational Scanning experiments
Luca Barbon, Victoria Offord, Elizabeth J. Radford…·Andrew J. Waters
Author
Wellcome Sanger Institute
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
5 papers
Recent·Most cited
Luca Barbon, Victoria Offord, Elizabeth J. Radford…·Andrew J. Waters
Bernardo Rodríguez–Martín, Eva G. Álvarez, Adrian Baez‐Ortega…·the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Network
The paper analyzes somatic retrotransposition events in 2,954 cancer genomes, identifying L1 insertions as significant contributors to structural variations and oncogenesis.
Francesco Iorio, Fiona M. Behan, Emanuel Gonçalves…·Mathew J. Garnett
CRISPRcleanR reduces false positives in CRISPR-Cas9 screens by correcting gene-independent responses without assuming copy number status.
Christina K. Yung, Brian D. O’Connor, Sergei Yakneen…·Charles L. Short
The paper describes the PCAWG project's large-scale analysis of cancer whole genomes across multiple computing environments, producing validated consensus variants for downstream research.
Ivo Buchhalter, Barbara Hutter, Tyler S. Alioto…·on behalf of the ICGC Verification and Validation Working Group
This study compares whole genome sequencing pipelines across five centers using a uniform tumor-normal sample pair, identifying factors affecting output consistency.