Selected publications
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Fast and scalable inference of multi-sample cancer lineages.
Genome Biology.
2015
Academic Article
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Times cited: 28 -
Characterization of Structural variants with single molecule and hybrid sequencing approaches.
Bioinformatics.
2014
Academic Article
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Times cited: 19 -
A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data.
Bioinformatics.
2014
Academic Article
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Times cited: 38 -
Detecting independent and recurrent copy number aberrations using interval graphs.
Bioinformatics.
2014
Academic Article
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Times cited: 10 -
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.
Nature Communications.
2014
Academic Article
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Times cited: 74 -
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
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Times cited: 6 -
MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels.
Bioinformatics.
2013
Academic Article
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Times cited: 22 -
An integrated map of genetic variation from 1,092 human genomes.
Nature.
2012
Academic Article
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Times cited: 2302 -
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.
Journal of Pathology.
2012
Academic Article
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Times cited: 82 -
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.
Journal of Pathology.
2012
Academic Article
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Times cited: 44 -
Mapping copy number variation by population-scale genome sequencing.
Nature.
2011
Academic Article
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Times cited: 476 -
A map of human genome variation from population-scale sequencing.
Nature.
2010
Academic Article
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Times cited: 4390 -
Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.
Bioinformatics.
2010
Academic Article
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Times cited: 60