publications
Pulled periodically from google scholar
2026
- Cancer CellThe ADAPT learning cancer treatment system: ARPA-H’s initiative to revolutionize cancer therapyCancer Cell, 2026
- Cell
2025
- Genome Res.OMKar automates genome karyotyping using optical maps to identify constitutional abnormalitiesGenome Research, 2025
- Nature Comms.Reconstructing the three-dimensional architecture of extrachromosomal DNA with ec3DNature Communications, 2025
- Cancer Discov.Extrachromosomal DNA–Driven Oncogene Spatial Heterogeneity and Evolution in GlioblastomaCancer Discovery, 2025
- Nature Cell BioEnhancer activation from transposable elements in extrachromosomal DNANature cell biology, 2025
- Adv. GeneticsRare Structural Variants Uncovered by Optical Genome Mapping in Multisystem Inflammatory Syndrome in Children (MIS-C)Advanced Genetics, 2025
- Nature GeneticsThree-dimensional genome landscape of primary human cancersNature Genetics, 2025
- RECOMBOMKar: Optical Map Based Automated Karyotyping of Genomes to Identify Constitutional DisordersIn International Conference on Research in Computational Molecular Biology, 2025
- PLOS Comp. Bio.Analysis of targeted and whole genome sequencing of PacBio HiFi reads for a comprehensive genotyping of gene-proximal and phenotype-associated Variable Number Tandem RepeatsPLOS Computational Biology, 2025
- Nature Comms.Inhibition of human-HPV hybrid ecDNA enhancers reduces oncogene expression and tumor growth in oropharyngeal cancerNature Communications, 2025
- Nature Comms.Breakage fusion bridge cycles drive high oncogene number with moderate intratumoural heterogeneityNature communications, 2025
- NatureEngineered extrachromosomal oncogene amplifications promote tumorigenesisNature, 2025
- Cancer Discov.Spatial–Temporal Diversity of Extrachromosomal DNA Shapes Urothelial Carcinoma Evolution and the Tumor Immune MicroenvironmentCancer discovery, 2025
- Cancer Discov.Disparate pathways for extrachromosomal DNA biogenesis and genomic DNA repairCancer Discovery, 2025
2024
- BloodA Single Mutation in the SENP1 Region Regulates the Excessive Erythropoiesis in the AndesBlood, 2024
- NatureOrigins and impact of extrachromosomal DNANature, 2024
- NatureEnhancing transcription–replication conflict targets ecDNA-positive cancersNature, 2024
- NatureCoordinated inheritance of extrachromosomal DNAs in cancer cellsNature, 2024
- ESMO Open111MO Extrachromosomal DNA drives oncogene spatial heterogeneity in IDH-wildtype glioblastomasESMO Open, 2024
- Nature GeneticsMapping extrachromosomal DNA amplifications during cancer progressionNature genetics, 2024
- JIDLB1067 Chromosomal structural variants but not extrachromosomal DNAs are common in Merkel cell carcinomaJournal of Investigative Dermatology, 2024
- Annals Oncol.Oncogenic extrachromosomal DNA identification using whole-genome sequencing from formalin-fixed glioblastomasAnnals of Oncology, 2024
- eLifeTranscriptional immune suppression and up-regulation of double-stranded DNA damage and repair repertoires in ecDNA-containing tumorsElife, 2024
- Genome Res.CoRAL accurately resolves extrachromosomal DNA genome structures with long-read sequencingGenome Research, 2024
2023
- DNA BarcodingAnalyses of nuclear reads obtained using genome skimmingIn DNA Barcoding: Methods and Protocols, 2023
- Environ. Intl.Multi-tissue proteogenomic analysis for mechanistic toxicology studies in non-model speciesEnvironment International, 2023
- Nature GeneticsCircular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastomaNature genetics, 2023
- Eur. J. Hum. Genet.Variable number tandem repeats (VNTRs) as modifiers of breast cancer risk in carriers of BRCA1 185delAGEuropean Journal of Human Genetics, 2023
- NatureEpigenetic dysregulation from chromosomal transit in micronucleiNature, 2023
- Bioinf. AdvancesTRviz: a Python library for decomposing and visualizing tandem repeat sequencesBioinformatics Advances, 2023
- NatureExtrachromosomal DNA in the cancerous transformation of Barrett’s oesophagusNature, 2023
- PNASIntegrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneityProceedings of the National Academy of Sciences, 2023
- Nature Comms.A deep population reference panel of tandem repeat variationNature Communications, 2023
2022
- METHODS AND COMPOSITIONS FOR DETECTING ecDNANov 2022US Patent App. 17/746,748
- Methods of diagnosing and treating cancer targeting extrachromosomal dnaFeb 2022US Patent App. 17/518,396
- Compositions and methods for modulating transcriptional activity of amplified oncogenes contained on extrachromosomal dnaJan 2022US Patent App. 17/311,980
- Targeting nad biosynthesis in the treatment of cancerMay 2022US Patent App. 17/438,610
- Cell Syst.Quantifying the uncertainty of assembly-free genome-wide distance estimates and phylogenetic relationships using subsamplingCell systems, 2022
- Nature CancerForm follows function in cancer genomesNature Cancer, 2022
- Nature GeneticsTargeted profiling of human extrachromosomal DNA by CRISPR-CATCHNature genetics, 2022
- iScienceOptical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19Iscience, 2022
- iScienceDetecting tandem repeat variants in coding regions using code-adVNTRIscience, 2022
- Eur. J. Hum. Genet.Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease studyEuropean Journal of Human Genetics, 2022
- ACM-BCBDeepViFi: detecting oncoviral infections in cancer genomes using transformersIn Proceedings of the 13th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics, 2022
- NatureMapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNANature, 2022
- RECOMBUncertainty quantification using subsampling for assembly-free estimates of genomic distance and phylogenetic relationshipsIn International Conference on Research in Computational Molecular Biology, 2022
- Ann. Rev. PathExtrachromosomal DNA: an emerging hallmark in human cancerAnnual Review of Pathology: Mechanisms of Disease, 2022
- Nature GeneticsThe evolutionary dynamics of extrachromosomal DNA in human cancersNature genetics, 2022
- Neuro-OncologyINTEGRATED ANALYSIS OF SINGLE CELL CHROMATIN ACCESSIBILITY AND RNA EXPRESSION IDENTIFIED COMMON VULNERABILITY DESPITE GLIOBLASTOMA HETEROGENEITYIn NEURO-ONCOLOGY, 2022
- NAR GenomicsFastViFi: Fast and accurate detection of (Hybrid) Viral DNA and RNANAR genomics and bioinformatics, 2022
- Ann. Rev. GHGExtrachromosomal DNA in cancerAnnual review of genomics and human genetics, 2022
- Hum. Mol. GeneticsHeterozygous Tropomodulin 3 mice have improved lung vascularization after chronic hypoxiaHuman Molecular Genetics, 2022
- Cancer Discov.Plasticity of extrachromosomal and intrachromosomal BRAF amplifications in overcoming targeted therapy dosage challengesCancer discovery, 2022
- ARID1B, a molecular suppressor of erythropoiesis, is essential for the prevention of Monge’s diseaseExperimental & molecular medicine, 2022
2021
- Methods of diagnosing and treating cancer targeting extrachromosomal DNADec 2021US Patent 11,193,164
- PLOS Comp. Bio.Estimating repeat spectra and genome length from low-coverage genome skims with RESPECTPLoS computational biology, 2021
- Extrachromosomal DNA (ecDNA) in cancer pathogenesisCurrent opinion in genetics & development, 2021
- Nature Comms.Multiple mechanisms drive genomic adaptation to extreme O2 levels in Drosophila melanogasterNature communications, 2021
- Clin Cancer ResExtrachromosomal DNA in HPV-mediated oropharyngeal cancer drives diverse oncogene transcriptionClinical Cancer Research, 2021
- NatureecDNA hubs drive cooperative intermolecular oncogene expressionNature, 2021
- ACM-BCBA CNN-based cell tracking method for multi-slice intravital imaging dataIn Proceedings of the 12th ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics, 2021
- Nature Comms.Variable number tandem repeats mediate the expression of proximal genesNature communications, 2021
- NAR GenomicsCONSULT: accurate contamination removal using locality-sensitive hashingNAR Genomics and Bioinformatics, 2021
- PatternsFaNDOM: Fast nested distance-based seeding of optical mapsPatterns, 2021
2020
- Nature Comms.Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cellsNature communications, 2020
- Nature Comms.AmpliconReconstructor integrates NGS and optical mapping to resolve the complex structures of focal amplificationsNature communications, 2020
- Mol. Ecol. Res.The impact of contaminants on the accuracy of genome skimming and the effectiveness of exclusion read filtersMolecular Ecology Resources, 2020
- FASEBIdentification of Candidate Genes Involved in the Survival of Drosophila in Extreme O2 EnvironmentsThe FASEB Journal, 2020
- Extrachromosomal DNA (ecDNA) carrying amplified oncogenes as a biomarker for insensitivity to pembrolizumab treatment in gastric cancer patients.2020
- Nature GeneticsExtrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancersNature genetics, 2020
- FASEBOxygen-Directed Laboratory Evolution and Conserved Mechanisms Underlying Hypoxia ToleranceThe FASEB Journal, 2020
- Beyond DNA barcoding: The unrealized potential of genome skim data in sample identification2020
- IJROBPLong-read RNA-Seq of human papillomavirus-associated head and neck cancer reveals novel alternatively spliced viral RNA isoformsInternational Journal of Radiation Oncology, Biology, Physics, 2020
- Nature Comms.
2019
- Methods of treating extrachromosomal dna expressing cancers2019
- Eur. J. Hum. Genet.Novel insight into the genetic basis of high-altitude pulmonary hypertension in Kyrgyz highlandersEuropean Journal of Human Genetics, 2019
- iScienceEcSeg: semantic segmentation of metaphase images containing extrachromosomal DNAIscience, 2019
- Nature Comms.Exploring the landscape of focal amplifications in cancer using AmpliconArchitectNature communications, 2019
- Genome Bio.Skmer: assembly-free and alignment-free sample identification using genome skimsGenome biology, 2019
- NatureCircular ecDNA promotes accessible chromatin and high oncogene expressionNature, 2019
- Nature Rev. CancerExtrachromosomal oncogene amplification in tumour pathogenesis and evolutionNature Reviews Cancer, 2019
- NatureNAD metabolic dependency in cancer is shaped by gene amplification and enhancer remodellingNature, 2019
- JPRProteogenomic annotation of Chinese hamsters reveals extensive novel translation events and endogenous retroviral elementsJournal of proteome research, 2019
- Cell SystComputing the statistical significance of overlap between genome annotations with iStatCell systems, 2019
2018
- Whole-Genome-Sequencing Reveals Involvement of Mitochondria-Dependent Apoptotic Genes in High Altitude Pulmonary HypertensionIn B108. PULMONARY HYPERTENSION: THE LATEST FINDINGS, 2018
- Genome Res.Targeted genotyping of variable number tandem repeats with adVNTRGenome research, 2018
- RECOMBTargeted Genotyping of Variable Number Tandem Repeats with AdVNTRIn Research in Computational Molecular Biology, 2018
- JPMHC class I loaded ligands from breast cancer cell lines: A potential HLA-I-typed antigen collectionJournal of proteomics, 2018
- Nuc. Acids. ResViFi: accurate detection of viral integration and mRNA fusion reveals indiscriminate and unregulated transcription in proximal genomic regions in cervical cancerNucleic acids research, 2018
- Nature MethodsIdentifying the favored mutation in a positive selective sweepNature methods, 2018
- Cell Syst.Proteostorm: An ultrafast metaproteomics database search frameworkCell systems, 2018
2017
- NatureExtrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneityNature, 2017
- The antibody repertoire of colorectal cancerMolecular & Cellular Proteomics, 2017
- BloodMolecular basis of hypoxia-induced excessive erythrocytosis: critical role of SENP1 gene regulationBlood, 2017
- Genome Res.HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologiesGenome research, 2017
- JMMHigh-altitude adaptation in humans: from genomics to integrative physiologyJournal of Molecular Medicine, 2017
- PNASUltraaccurate genome sequencing and haplotyping of single human cellsProceedings of the National Academy of Sciences, 2017
- Mol Biol. Evol.New insights into the genetic basis of Monge’s disease and adaptation to high-altitudeMolecular biology and evolution, 2017
- GeneticsCLEAR: Composition of likelihoods for evolve and resequence experimentsGenetics, 2017
2016
- CellIntegrated proteogenomic characterization of human high-grade serous ovarian cancerCell, 2016
- Nuc. Acids. ResInPhaDel: integrative shotgun and proximity-ligation sequencing to phase deletions with single nucleotide polymorphismsNucleic acids research, 2016
- PLOS Genet.Correction: Predicting Carriers of Ongoing Selective Sweeps without Knowledge of the Favored AllelePLoS genetics, 2016
- JEDSenp1 drives hypoxia-induced polycythemia via GATA1 and Bcl-xL in subjects with Monge’s diseaseJournal of Experimental Medicine, 2016
- Appl. Environ. Microbiol.Diversity, productivity, and stability of an industrial microbial ecosystemApplied and environmental microbiology, 2016
2015
- ACS Infect. Dis.Next-generation sequencing of Plasmodium vivax patient samples shows evidence of direct evolution in drug-resistance genesACS infectious diseases, 2015
- Genet. Epidem.Genetic simulation tools for post-genome wide association studies of complex diseasesGenetic epidemiology, 2015
- JCBReconstructing breakage fusion bridge architectures using noisy copy numbersJournal of Computational Biology, 2015
- PNASEndothelin receptor B, a candidate gene from human studies at high altitude, improves cardiac tolerance to hypoxia in genetically engineered heterozygote miceProceedings of the National Academy of Sciences, 2015
- PLOS Genet.Predicting carriers of ongoing selective sweeps without knowledge of the favored allelePLoS genetics, 2015
- CirculationHeterozygous Endothelin Receptor Type B Knockout Confers Cardiac Resistance to Extreme Hypoxia in MiceCirculation, 2015
- PLOS OneThe TGF\beta1 promoter SNP C-509T and food sensitization promote esophageal remodeling in pediatric eosinophilic esophagitisPloS one, 2015
- JPRAdvanced proteogenomic analysis reveals multiple peptide mutations and complex immunoglobulin peptides in colon cancerJournal of proteome research, 2015
- RECOMBHaplotype Allele Frequency (HAF) score: predicting carriers of ongoing selective sweeps without knowledge of the adaptive alleleIn International Conference on Research in Computational Molecular Biology, 2015
2014
- ProteomicsProteogenomic strategies for identification of aberrant cancer peptides using large-scale next-generation sequencing dataProteomics, 2014
- Genome Bio.Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genesGenome biology, 2014
- Genome Res.Amplification and thrifty single-molecule sequencing of recurrent somatic structural variationsGenome Research, 2014
- Nuc. Acids. ResThe elusive evidence for chromothripsisNucleic acids research, 2014
- Annotation of the zebrafish genome through an integrated transcriptomic and proteomic analysisMolecular & cellular proteomics, 2014
- An automated proteogenomic method uses mass spectrometry to reveal novel genes in Zea maysMolecular & Cellular Proteomics, 2014
- Phys.The genetic basis of chronic mountain sicknessPhysiology, 2014
- BioinformaticsInferring gene ontologies from pairwise similarity dataBioinformatics, 2014
- JPRProteogenomic database construction driven from large scale RNA-seq dataJournal of proteome research, 2014
- BioinformaticsUsing Genome Query Language to uncover genetic variationBioinformatics, 2014
2013
- AJHGWhole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlandersThe American Journal of Human Genetics, 2013
- BioinformaticsWessim: a whole-exome sequencing simulator based on in silico exome captureBioinformatics, 2013
- Genome Bio.On the design of clone-based haplotypingGenome biology, 2013
- CACMAbstractions for genomicsCommunications of the ACM, 2013
- Nuc. Acids. ResReprever: resolving low-copy duplicated sequences using template driven assemblyNucleic acids research, 2013
- GeneticsLearning natural selection from the site frequency spectrumGenetics, 2013
- PNASAn algorithmic approach for breakage-fusion-bridge detection in tumor genomesProceedings of the National Academy of Sciences, 2013
- BMC Bioinform.Evaluating genome architecture of a complex region via generalized bipartite matchingBMC bioinformatics, 2013
- Genome Bio.Virmid: accurate detection of somatic mutations with sample impurity inferenceGenome biology, 2013
- WABICerulean: a hybrid assembly using high throughput short and long readsIn International workshop on algorithms in bioinformatics, 2013
2012
- BioinformaticsSpeeding up tandem mass spectral identification using indexesBioinformatics, 2012
- Genome Res.Global DNA hypomethylation coupled to repressive chromatin domain formation and gene silencing in breast cancerGenome research, 2012
- JCBCombinatorics of the breakage-fusion-bridge mechanismJournal of Computational Biology, 2012
- JCBAccurate mass spectrometry based protein quantification via shared peptidesJournal of Computational Biology, 2012
- Nature GeneticsDe novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephalyNature genetics, 2012
- RECOMBModeling the breakage-fusion-bridge mechanism: combinatorics and cancer genomicsIn Annual International Conference on Research in Computational Molecular Biology, 2012
- PLOS OneSample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approachPLoS One, 2012
- JAMIAiDASH: integrating data for analysis, anonymization, and sharingJournal of the American Medical Informatics Association, 2012
- Sci. Trans. MedExome sequencing can improve diagnosis and alter patient managementScience translational medicine, 2012
2011
- AF: Small: Algorithms for Genetics: Epistatic Interactions, Haplotype Assembly, and Selection SignaturesNSF Award Number 1115206. Directorate for Computer and Information Science and Engineering, 2011
- JPRAutomated querying and identification of novel peptides using MALDI mass spectrometric imagingJournal of proteome research, 2011
- JCBPreface: satellite workshop on comparative genomics, research in computational molecular biology (RECOMB-CG 2010) prefaceJournal of Computational Biology, 2011
- ACM-BCB2011 Index IEEE/ACM Transactions on Computational Biology and Bioinformatics Vol. 8IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2011
- On the approximability of reachability-preserving network orientationsInternet Mathematics, 2011
- Visualization of the MS-Align algorithm results for the protein spectrum matchesDepartment of Bioengineering and Bioinformatics of MV Lomonosov Moscow State University, 2011
- JPRAMASS: algorithm for MSI analysis by semi-supervised segmentationJournal of proteome research, 2011
- JPRPractical 4-phosphopantetheine active site discovery from proteomic samplesJournal of proteome research, 2011
- Front. Genet.Tests of selection in pooled case-control data: an empirical studyFrontiers in Genetics, 2011
- PNASExperimental selection of hypoxia-tolerant Drosophila melanogasterProceedings of the National Academy of Sciences, 2011
- On the Approximability of Reachability-Preserving Network OrientationsInternet Mathematics, 2011
- Metabolic Network Analysis Demystified. Ed. Vineet Bafna, S. Cenk Shinalp. LNCS Sublibrary: SL 8-Bioinformatics2011
- BioinformaticsSensitive gene fusion detection using ambiguously mapping RNA-Seq read pairsBioinformatics, 2011
- Research in Computational Molecular Biology: 15th Annual International Conference, RECOMB 2011, Vancouver, BC, Canada, March 28-31, 2011. Proceedings2011
- BMC Bioinform.Strobe sequence design for haplotype assemblyBMC bioinformatics, 2011
- JCBCompressing genomic sequence fragments using SlimGeneJournal of Computational Biology, 2011
- ProteomicsResurrection of a clinical antibody: Template proteogenomic de novo proteomic sequencing and reverse engineering of an anti-lymphotoxin-αantibodyProteomics, 2011
2010
- Genome Bio.Deciphering the genetic basis of common diseases by integrated functional annotation of common and rare variantsGenome Biology, 2010
- BMC GenomicsConstruction of a medicinal leech transcriptome database and its application to the identification of leech homologs of neural and innate immune genesBMC genomics, 2010
- PLOS Comp. Bio.A covering method for detecting genetic associations between rare variants and common phenotypesPLoS computational biology, 2010
- FASEBMapping of peptides and proteins in Leech (Hirudo medicinalis) by Mass Spectrometry ImagingThe FASEB Journal, 2010
- JPProteogenomics to discover the full coding content of genomes: a computational perspectiveJournal of proteomics, 2010
- BioinformaticsRAPID detection of gene–gene interactions in genome-wide association studiesBioinformatics, 2010
- ACM-BCBTCLUST: A fast method for clustering genome-scale expression dataIEEE/ACM transactions on computational biology and bioinformatics, 2010
- Template proteogenomics: sequencing whole proteins using an imperfect databaseMolecular & Cellular Proteomics, 2010
- Genome Bio.Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite levelGenome biology, 2010
- BMC GenomicsDesigning deep sequencing experiments: detecting structural variation and estimating transcript abundanceBMC genomics, 2010
- MBIOExpansion of the mycobacterial “PUPylome”Molecular bioSystems, 2010
- Deconvolution and database search of complex tandem mass spectra of intact proteinsMolecular & Cellular Proteomics, 2010
- JCBProtein-protein interaction network evaluation for identifying potential drug targetsJournal of Computational Biology, 2010
- BMC GenomicsConstruction of a medicinal leech transcriptome database and its application to the identification of leech homologs of neural and innate immune genesBMC Genomics, 2010
- JCBOptimizing PCR assays for DNA-based cancer diagnosticsJournal of Computational Biology, 2010
- RECOMBCompressing genomic sequence fragments using SlimGeneIn Annual International Conference on Research in Computational Molecular Biology, 2010
2009
- RECOMB
- JCBFast and accurate alignment of multiple protein networksJournal of computational biology, 2009
- Genome Res.Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encodingGenome research, 2009
2008
- BioinformaticsHapCUT: an efficient and accurate algorithm for the haplotype assembly problemBioinformatics, 2008
- RECOMBQnet: A tool for querying biological networksRECOMB 2007 and JCB, 2008
- RECOMBFast and accurate alignment of multiple protein networksIn Annual International Conference on Research in Computational Molecular Biology, 2008
- A multidimensional chromatography technology for in-depth phosphoproteome analysisMolecular & Cellular Proteomics, 2008
- Genome Res.Comparative proteogenomics: combining mass spectrometry and comparative genomics to analyze multiple genomesGenome research, 2008
- PLOS Comp. Bio.Evaluation of paired-end sequencing strategies for detection of genome rearrangements in cancerPLoS computational biology, 2008
- JCBStructural alignment of pseudoknotted RNAJournal of Computational Biology, 2008
- PNASDiscovery and revision of Arabidopsis genes by proteogenomicsProceedings of the national academy of sciences, 2008
- JPRAccurate annotation of peptide modifications through unrestrictive database searchJournal of proteome research, 2008
- WABIAn algorithm for orienting graphs based on cause-effect pairs and its applications to orienting protein networksIn International Workshop on Algorithms in Bioinformatics, 2008
- JPRPhosphorylation-specific MS/MS scoring for rapid and accurate phosphoproteome analysisJournal of proteome research, 2008
- Genome Res.An MCMC algorithm for haplotype assembly from whole-genome sequence dataGenome research, 2008
2007
- Phosphorylation-specific MS/MS scoringMolecular & Cellular Proteomics, 2007
- BioinformaticsOptimization of primer design for the detection of variable genomic lesions in cancerBioinformatics, 2007
- Systems Biology and Computational Proteomics: Joint RECOMB 2006 Satellite Workshops on Systems Biology, and on Computational Proteomics, San Diego, CA, USA, December 1-3, 2006, Revised Selected Papers2007
- Genome Res.Improving gene annotation using peptide mass spectrometryGenome research, 2007
- PLOS BioThe Sorcerer II Global Ocean Sampling expedition: expanding the universe of protein familiesPLoS biology, 2007
- PLOS BioThe diploid genome sequence of an individual humanPLoS biology, 2007
- Genome Res.Evidence for large inversion polymorphisms in the human genome from HapMap dataGenome research, 2007
- Genome Res.Whole proteome analysis of post-translational modifications: applications of mass-spectrometry for proteogenomic annotationGenome research, 2007
- JCBA decomposition theory for phylogenetic networks and incompatible charactersJournal of Computational Biology, 2007
- Mol. Syst. Bio.Integrating scientific culturesMolecular Systems Biology, 2007
- RECOMBQNet: a tool for querying protein interaction networksIn Annual International Conference on Research in Computational Molecular Biology, 2007
2006
- JCBConsensus folding of unaligned RNA sequences revisitedJournal of computational biology, 2006
- Identification of informative genetic markersMar 2006US Patent App. 11/040,652
- JPRAge-related changes in human crystallins determined from comparative analysis of post-translational modifications in young and aged lens: does deamidation contribute to crystallin insolubility?Journal of proteome research, 2006
- BioinformaticsA sequence-based filtering method for ncRNA identification and its application to searching for riboswitch elementsBioinformatics, 2006
- JCBInference about recombination from haplotype data: lower bounds and recombination hotspotsJournal of Computational Biology, 2006
- RECOMBStructural alignment of pseudoknotted RNAIn Annual International Conference on Research in Computational Molecular Biology, 2006
- CSBEXPLORING THE OCEAN’S MICROBES: SEQUENCING THE SEVEN SEASIn Computational Systems Bioinformatics, 2006
- Nature ProtocolsUnrestrictive identification of post-translational modifications through peptide mass spectrometryNature protocols, 2006
2005
- ACM-BCB2005 Index IEEE/ACM Transactions on Computational Biology and Bioinformatics Vol. 2IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2005
- JPRPeptide sequence tags for fast database search in mass-spectrometryJournal of proteome research, 2005
- ACM-BCBSearching genomes for noncoding RNA using FastRIEEE/ACM Transactions on Computational Biology and Bioinformatics, 2005
- Genome Res.Orthologous repeats and mammalian phylogenetic inferenceGenome Research, 2005
- Identification of post-translational modifications via blind search of mass-spectraIn 2005 IEEE Computational Systems Bioinformatics Conference (CSB’05), 2005
- Theor. Comp. Sci.Polynomial and APX-hard cases of the individual haplotyping problemTheoretical Computer Science, 2005
- RECOMBConsensus folding of unaligned RNA sequences revisitedIn Annual International Conference on Research in Computational Molecular Biology, 2005
- Anal. Chem.InsPecT: identification of posttranslationally modified peptides from tandem mass spectraAnalytical chemistry, 2005
- RECOMBImproved recombination lower bounds for haplotype dataIn Annual International Conference on Research in Computational Molecular Biology, 2005
2004
- IEEE CSBFastR: Fast database search tool for non-coding RNAIn Proceedings. 2004 IEEE Computational Systems Bioinformatics Conference, 2004. CSB 2004., 2004
- JCBA note on efficient computation of haplotypes via perfect phylogenyJournal of Computational Biology, 2004
- ACM-BCBThe number of recombination events in a sample history: conflict graph and lower boundsIEEE/ACM Transactions on Computational Biology and Bioinformatics, 2004
- Genome Res.Optimal haplotype block-free selection of tagging SNPs for genome-wide association studiesGenome research, 2004
- Anal. Chem.Shotgun protein sequencing by tandem mass spectra assemblyAnalytical chemistry, 2004
- Mass spectrometry and computational proteomicsEncyclopedia of Genetics, Genomics, Proteomics and Bioinformatics, 2004
2003
- RECOMBHaplotypes and informative SNP selection algorithms: don’t block out informationIn Proceedings of the seventh annual international conference on Research in computational molecular biology, 2003
- JCBRobustness of inference of haplotype block structureJournal of Computational Biology, 2003
- ScienceThe dog genome: survey sequencing and comparative analysisScience, 2003
- DMTCSCombinatorial problems arising in SNP and haplotype analysisIn International Conference on Discrete Mathematics and Theoretical Computer Science, 2003
- RECOMBOn de novo interpretation of tandem mass spectra for peptide identificationIn Proceedings of the seventh annual international conference on Research in computational molecular biology, 2003
- JCBHaplotyping as perfect phylogeny: A direct approachJournal of Computational Biology, 2003
2002
- RECOMB WorkshopHaplotyping as perfect phylogenyIn RECOMB Workshop on Computational Methods for SNPs and Haplotype Inference, 2002
- UC Davis Computer Science Technical Report CSE-2002-212002
- RECOMB WorkshopA survey of computational methods for determining haplotypesIn RECOMB Workshop on Computational Methods for SNPs and Haplotype Inference, 2002
- WABIPractical algorithms and fixed-parameter tractability for the single individual SNP haplotyping problemIn International Workshop on Algorithms in Bioinformatics, 2002
2001
- ScienceThe sequence of the human genomeScience, 2001
- SNPs Problems, Complexity, and AlgorithmsIn Proceedings of the 9th Annual European Symposium on Algorithms, 2001
- ScienceThe sequence of the human genomescience, 2001
- BioinformaticsSCOPE: a probabilistic model for scoring tandem mass spectra against a peptide databaseBioinformatics, 2001
2000
- Comp. Gen.Circular permutations and genome shufflingIn Comparative Genomics: Empirical and Analytical Approaches to Gene Order Dynamics, Map Alignment and the Evolution of Gene Families, 2000
- JCBLigand-receptor pairing via tree comparisonJournal of Computational Biology, 2000
1999
- SIAM Disc. Math.A 2-approximation algorithm for the undirected feedback vertex set problemSIAM Journal on Discrete Mathematics, 1999
1998
- JCIHuman beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung.The Journal of clinical investigation, 1998
- RECOMBDetecting non-adjoining correlations with signals in DNAIn Proceedings of the second annual international conference on Computational molecular biology, 1998
- ISMBThe ribosome scanning model for translation initiation: implications for gene prediction and full-length cDNA detection.In ISMB, 1998
- SODAA polynomial time approximation scheme for minimum routing cost spanning treesIn Proceedings of the Ninth Annual ACM-SIAM Symposium on Discrete Algorithms, San Francisco, California, USA, 1998
- SIAM Disc. Math.Sorting by transpositionsSIAM Journal on Discrete Mathematics, 1998
1997
- Theor. Comp. Sci.with two errors (Mathematical Games)Theoretical Computer Science, 1997
- Theor. Comp. Sci.Approximation algorithms for multiple sequence alignmentTheoretical Computer Science, 1997
1996
- DAMNonoverlapping local alignments (weighted independent sets of axis-parallel rectangles)Discrete Applied Mathematics, 1996
- SIAM ComputingGenome rearrangements and sorting by reversalsSIAM Journal on computing, 1996
- Constant ratio approximations of feedback vertex sets in weighted undirected graphs1996
- Constant Ratio Approximations of Feedback Vertex Sets inWeighted Undirected Graphs1996
1995
- ISAACConstant ratio approximations of the weighted feedback vertex set problem for undirected graphsIn International Symposium on Algorithms and Computation, 1995
- CPMComputing similarity between RNA stringsIn Annual Symposium on Combinatorial Pattern Matching, 1995
- WADSNonoverlapping local alignments (weighted independent sets of axis parallel rectangles)In Workshop on Algorithms and Data Structures, 1995
1994
- Approximation algorithms for multiple alignment and genome rearrangements1994
- CPMApproximation algorithms for multiple sequence alignmentIn Annual Symposium on Combinatorial Pattern Matching, 1994
- Theor. Comp. Sci.Not all insertion methods yield constant approximate tours in the Euclidean planeTheoretical Computer Science, 1994
1990
- VECPARParallel implementation of logic languagesIn International Conference on Vector and Parallel Processing, 1990