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Author Details

Mark Diekhans
Genomics Institute, University of California Santa Cruz
1999
90
59
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36420891The UCSC Genome Browser database: 2023 update.Nucleic Acids Res2023
36420896GENCODE: reference annotation for the human and mouse genomes in 2023.Nucleic Acids Res2023
36420891The UCSC Genome Browser database: 2023 update.Nucleic Acids Res2023
38077089The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes.bioRxiv2023
37612512The complete sequence of a human Y chromosome.Nature2023
37066387Single-cell long-read mRNA isoform regulation is pervasive across mammalian brain regions, cell types, and development.bioRxiv2023
37104599Evolutionary constraint and innovation across hundreds of placental mammals.Science2023
37546854Systematic assessment of long-read RNA-seq methods for transcript identification and quantification.bioRxiv2023
38077089The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes.bioRxiv2023
37612512The complete sequence of a human Y chromosome.Nature2023
37546854Systematic assessment of long-read RNA-seq methods for transcript identification and quantification.bioRxiv2023
37104599Evolutionary constraint and innovation across hundreds of placental mammals.Science2023
37066387Single-cell long-read mRNA isoform regulation is pervasive across mammalian brain regions, cell types, and development.bioRxiv2023
36420896GENCODE: reference annotation for the human and mouse genomes in 2023.Nucleic Acids Res2023
34718705The UCSC Genome Browser database: 2022 update.Nucleic Acids Res2022
35357917Segmental duplications and their variation in a complete human genome.Science2022
34728536Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing.RNA2022
34718705The UCSC Genome Browser database: 2022 update.Nucleic Acids Res2022
35357917Segmental duplications and their variation in a complete human genome.Science2022
34728536Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing.RNA2022
33270111GENCODE 2021.Nucleic Acids Res2021
33911273Towards complete and error-free genome assemblies of all vertebrate species.Nature2021
33953399A high-quality bonobo genome refines the analysis of hominid evolution.Nature2021
33833441Author Correction: Dense sampling of bird diversity increases power of comparative genomics.Nature2021
33221922The UCSC Genome Browser database: 2021 update.Nucleic Acids Res2021
33270111GENCODE 2021.Nucleic Acids Res2021
33911273Towards complete and error-free genome assemblies of all vertebrate species.Nature2021
33833441Author Correction: Dense sampling of bird diversity increases power of comparative genomics.Nature2021
33953399A high-quality bonobo genome refines the analysis of hominid evolution.Nature2021
33221922The UCSC Genome Browser database: 2021 update.Nucleic Acids Res2021
32434849AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature.Sci Transl Med2020
32434849AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature.Sci Transl Med2020
31691824UCSC Genome Browser enters 20th year.Nucleic Acids Res2020
32463100halSynteny: a fast, easy-to-use conserved synteny block construction method for multiple whole-genome alignments.Gigascience2020
33177665Dense sampling of bird diversity increases power of comparative genomics.Nature2020
33177663Progressive Cactus is a multiple-genome aligner for the thousand-genome era.Nature2020
33335035Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility.Science2020
32728065Transcriptional activity and strain-specific history of mouse pseudogenes.Nat Commun2020
31691824UCSC Genome Browser enters 20th year.Nucleic Acids Res2020
33335035Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility.Science2020
33177665Dense sampling of bird diversity increases power of comparative genomics.Nature2020
33177663Progressive Cactus is a multiple-genome aligner for the thousand-genome era.Nature2020
32728065Transcriptional activity and strain-specific history of mouse pseudogenes.Nat Commun2020
32463100halSynteny: a fast, easy-to-use conserved synteny block construction method for multiple whole-genome alignments.Gigascience2020
30407534The UCSC Genome Browser database: 2019 update.Nucleic Acids Res2019
31814998Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>.NPJ Genom Med2019
30407534The UCSC Genome Browser database: 2019 update.Nucleic Acids Res2019
30357393GENCODE reference annotation for the human and mouse genomes.Nucleic Acids Res2019
30379572Whole-Genome Alignment and Comparative Annotation.Annu Rev Anim Biosci2019
31814998Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>.NPJ Genom Med2019
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Collaborators

Genomics Institute, University of California Santa Cruz
Co-authored papers 55
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UC Santa Cruz Genomics Institute, University of California
Co-authored papers 24
Genomics Institute, University of California Santa Cruz
Co-authored papers 22
Co-authored papers 21
Co-authored papers 21
Co-authored papers 20
Co-authored papers 20
Co-authored papers 20
Genomics Institute, University of California Santa Cruz
Co-authored papers 20
Co-authored papers 18
Co-authored papers 15
Liver Center and Diabetes Center, University of California san francisco
Co-authored papers 13
Genomics Institute, University of California Santa Cruz
Co-authored papers 12
Genomics Institute, University of California Santa Cruz
Co-authored papers 12
Genomics Institute, University of California Santa Cruz
Co-authored papers 11
Center for Biomolecular Science and Engineering, University of California
Co-authored papers 11
Co-authored papers 10
Co-authored papers 10
Co-authored papers 9
European Bioinformatics Institute
Co-authored papers 9
Co-authored papers 9
Yale University
Co-authored papers 8
Johns Hopkins University
Co-authored papers 8
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University of Washington
Co-authored papers 7
Barcelona Institute of Science and Technology
Co-authored papers 7
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Institut fur Mathematik und Informatik, Universitat Greifswald
Co-authored papers 6
UC Santa Cruz Genomics Institute, University of California
Co-authored papers 6