Selected publications
- Fast and scalable inference of multi-sample cancer lineages. Genome biology. 2015 Academic Article GET IT
- Characterization of structural variants with single molecule and hybrid sequencing approaches. Bioinformatics (Oxford, England). 2014 Academic Article GET IT
- A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data. Bioinformatics (Oxford, England). 2014 Academic Article GET IT
- Detecting independent and recurrent copy number aberrations using interval graphs. Bioinformatics (Oxford, England). 2014 Academic Article GET IT
- Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature communications. 2014 Academic Article GET IT
- Reconstructing mutational history in multiply sampled tumors using perfect phylogeny mixtures. Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 2014 Conference Paper GET IT
- MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels. Bioinformatics (Oxford, England). 2013 Academic Article GET IT
- An integrated map of genetic variation from 1,092 human genomes. Nature. 2012 Academic Article GET IT
- From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer. The Journal of pathology. 2012 Academic Article GET IT
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Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.
The Journal of pathology.
2012
Academic Article
GET IT
Times cited: 3 - Mapping copy number variation by population-scale genome sequencing. Nature. 2011 Academic Article GET IT
- A map of human genome variation from population-scale sequencing. Nature. 2010 Academic Article GET IT
- Detection and characterization of novel sequence insertions using paired-end next-generation sequencing. Bioinformatics (Oxford, England). 2010 Academic Article GET IT