Haussler, David
Howard Hughes Medical Institute · University of California, Santa Cruz
66 papers on CoChatORCID 0000-0003-1533-4575
Most cited papers
- Verified
Genome-wide bioinformatic and molecular analysis of introns in Saccharomyces cerevisiae
SPINGOLA, M., GRATE, L., HAUSSLER, D., & ARES, M. (1999) · RNA
RNA Research and SplicingGenomics and Phylogenetic Studies
Cited by 316
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Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Akdemir, K. C., Le, V. T., Chandran, S., Li, Y., Verhaak, R. G., Beroukhim, R., Campbell, P. J., Chin, L., Dixon, J. R., Futreal, P. A., et al. (2020) · Nature Genetics
Genomics and Chromatin DynamicsChromatin Remodeling and Cancer
Cited by 283
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The UCSC Genome Browser database: 2022 update
Lee, B. T., Barber, G. P., Benet-Pagès, A., Casper, J., Clawson, H., Diekhans, M., Fischer, C., Gonzalez, J. N., Hinrichs, A. S., Lee, C. M., et al. (2022) · Nucleic Acids Research
Genomics and Phylogenetic StudiesGenetics, Bioinformatics, and Biomedical Research
Cited by 273
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HAL: a hierarchical format for storing and analyzing multiple genome alignments
Hickey, G., Paten, B., Earl, D., Zerbino, D., & Haussler, D. (2013) · Bioinformatics
Genomics and Phylogenetic StudiesGenome Rearrangement Algorithms
Cited by 272
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Cactus: Algorithms for genome multiple sequence alignment
Paten, B., Earl, D., Nguyen, N., Diekhans, M., Zerbino, D., & Haussler, D. (2011) · Genome Research
Genomics and Phylogenetic StudiesGenome Rearrangement Algorithms
Cited by 243
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Semi-automated assembly of high-quality diploid human reference genomes
Jarvis, E. D., Formenti, G., Rhie, A., Guarracino, A., Yang, C., Wood, J., Tracey, A., Thibaud-Nissen, F., Vollger, M. R., Porubsky, D., et al. (2022) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 209
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UCSC Genome Browser enters 20th year
Lee, C. M., Barber, G. P., Casper, J., Clawson, H., Diekhans, M., Gonzalez, J. N., Hinrichs, A. S., Lee, B. T., Nassar, L. R., Powell, C. C., et al. (2019) · Nucleic Acids Research
Genomics and Phylogenetic StudiesGenetics, Bioinformatics, and Biomedical Research
Cited by 191
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Comprehensive pan-genomic characterization of adrenocortical carcinoma
Zheng, S., Cherniack, A. D., Dewal, N., Moffitt, R. A., Danilova, L., Murray, B. A., Lerario, A. M., Else, T., Knijnenburg, T. A., Ciriello, G., et al. (2016) · Cancer Cell
Adrenal and Paraganglionic TumorsChromatin Remodeling and Cancer
Cited by 165
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Recombination between heterologous human acrocentric chromosomes
Guarracino, A., Buonaiuto, S., de Lima, L. G., Potapova, T., Rhie, A., Koren, S., Rubinstein, B., Fischer, C., Human Pangenome Reference Consortium, Abel, H. J., et al. (2023) · Nature
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 134
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Comparative Genomics Search for Losses of Long-Established Genes on the Human Lineage
Zhu, J., Sanborn, J. Z., Diekhans, M., Lowe, C. B., Pringle, T. H., & Haussler, D. (2007) · PLoS Computational Biology
Chromosomal and Genetic VariationsGenomics and Phylogenetic Studies
Cited by 129
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Comparative Annotation Toolkit (CAT)—simultaneous clade and personal genome annotation
Fiddes, I. T., Armstrong, J., Diekhans, M., Nachtweide, S., Kronenberg, Z. N., Underwood, J. G., Gordon, D., Earl, D., Keane, T., Eichler, E. E., et al. (2018) · Genome Research
Genomics and Phylogenetic StudiesChromosomal and Genetic Variations
Cited by 120
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Alignathon: a competitive assessment of whole-genome alignment methods
Earl, D., Nguyen, N., Hickey, G., Harris, R. S., Fitzgerald, S., Beal, K., Seledtsov, I., Molodtsov, V., Raney, B. J., Clawson, H., et al. (2014) · Genome Research
Genomics and Phylogenetic StudiesGenome Rearrangement Algorithms
Cited by 113
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Biased clustered substitutions in the human genome: The footprints of male-driven biased gene conversion
Dreszer, T. R., Wall, G. D., Haussler, D., & Pollard, K. S. (2007) · Genome Research
Chromosomal and Genetic VariationsEvolution and Genetic Dynamics
Cited by 112
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Increased mutation and gene conversion within human segmental duplications
Vollger, M. R., Dishuck, P. C., Harvey, W. T., DeWitt, W. S., Guitart, X., Goldberg, M. E., Rozanski, A. N., Lucas, J., Asri, M., Human Pangenome Reference Consortium, et al. (2023) · Nature
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 104
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Cactus Graphs for Genome Comparisons
Paten, B., Diekhans, M., Earl, D., John, J. S., Ma, J., Suh, B., & Haussler, D. (2011) · Journal of Computational Biology
Genome Rearrangement AlgorithmsGenomics and Phylogenetic Studies
Cited by 102
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The Share of Human Genomic DNA under Selection Estimated from Human-Mouse Genomic Alignments
CHIAROMONTE, F., WEBER, R. J., ROSKIN, K. M., DIEKHANS, M., KENT, W. J., & HAUSSLER, D. (2003) · Cold Spring Harbor Symposia on Quantitative Biology
Genomics and Phylogenetic StudiesEvolution and Genetic Dynamics
Cited by 64
- Verified
Barriers to accessing public cancer genomic data
Learned, K., Durbin, A., Currie, R., Kephart, E. T., Beale, H. C., Sanders, L. M., Pfeil, J., Goldstein, T. C., Salama, S. R., Haussler, D., et al. (2019) · Scientific Data
Research Data Management PracticesEthics in Clinical Research
Cited by 34
- Verified
Scoring two-species local alignments to try to statistically separate neutrally evolving from selected DNA segments
Roskin, K. M., Diekhans, M., & Haussler, D. (2003) · Proceedings of the seventh annual international conference on Research in computational molecular biology
Genomics and Phylogenetic StudiesFractal and DNA sequence analysis
Cited by 14
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