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Author Details

Deanna M Church
Present address: Inscripta Inc.
1992
86
52
Christopher Churas (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35886053A Chromosome-Length Assembly of the Hawaiian Monk Seal (<i>Neomonachus schauinslandi</i>): A History of "Genetic Purging" and Genomic Stability.Genes (Basel)2022
35886053A Chromosome-Length Assembly of the Hawaiian Monk Seal (<i>Neomonachus schauinslandi</i>): A History of "Genetic Purging" and Genomic Stability.Genes (Basel)2022
35864110Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2022
35357937A next-generation human genome sequence.Science2022
35357937A next-generation human genome sequence.Science2022
35864110Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2022
32228451De novo assembly of the olive fruit fly (Bactrocera oleae) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly.BMC Genomics2020
31964885Haplotyping the Vitis collinear core genome with rhAmpSeq improves marker transferability in a diverse genus.Nat Commun2020
32228451De novo assembly of the olive fruit fly (Bactrocera oleae) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly.BMC Genomics2020
32461645Thousands of human sequences provide deep insight into single genomes.Nature2020
33125890Single-Cell Transcriptomics Reveals Early Emergence of Liver Parenchymal and Non-parenchymal Cell Lineages.Cell2020
31964885Haplotyping the Vitis collinear core genome with rhAmpSeq improves marker transferability in a diverse genus.Nat Commun2020
33125890Single-Cell Transcriptomics Reveals Early Emergence of Liver Parenchymal and Non-parenchymal Cell Lineages.Cell2020
32461645Thousands of human sequences provide deep insight into single genomes.Nature2020
30959515The emergent landscape of the mouse gut endoderm at single-cell resolution.Nature2019
31610793Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome.Genome Biol2019
30959515The emergent landscape of the mouse gut endoderm at single-cell resolution.Nature2019
31413257A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2019
31413257A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2019
31610793Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome.Genome Biol2019
29610250Corrigendum: Direct determination of diploid genome sequences.Genome Res2018
30188541Genomes for all.Nat Biotechnol2018
29610250Corrigendum: Direct determination of diploid genome sequences.Genome Res2018
29474918Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.Cell2018
29423234Reference quality assembly of the 3.5-Gb genome of <i>Capsicum annuum</i> from a single linked-read library.Hortic Res2018
30188541Genomes for all.Nat Biotechnol2018
29474918Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.Cell2018
29423234Reference quality assembly of the 3.5-Gb genome of <i>Capsicum annuum</i> from a single linked-read library.Hortic Res2018
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
28381613Direct determination of diploid genome sequences.Genome Res2017
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
28122645A variant by any name: quantifying annotation discordance across tools and clinical databases.Genome Med2017
28315672Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.J Mol Diagn2017
28315672Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.J Mol Diagn2017
28381613Direct determination of diploid genome sequences.Genome Res2017
28122645A variant by any name: quantifying annotation discordance across tools and clinical databases.Genome Med2017
27964746Alternate-locus aware variant calling in whole genome sequencing.Genome Med2016
26578580Assembly: a resource for assembled genomes at NCBI.Nucleic Acids Res2016
27964746Alternate-locus aware variant calling in whole genome sequencing.Genome Med2016
26578580Assembly: a resource for assembled genomes at NCBI.Nucleic Acids Res2016
25651527Extending reference assembly models.Genome Biol2015
25651527Extending reference assembly models.Genome Biol2015
26269718Achieving high-sensitivity for clinical applications using augmented exome sequencing.Genome Med2015
26154004Good laboratory practice for clinical next-generation sequencing informatics pipelines.Nat Biotechnol2015
26269718Achieving high-sensitivity for clinical applications using augmented exome sequencing.Genome Med2015
26154004Good laboratory practice for clinical next-generation sequencing informatics pipelines.Nat Biotechnol2015
24234437ClinVar: public archive of relationships among sequence variation and human phenotype.Nucleic Acids Res2014
25373144Single haplotype assembly of the human genome from a hydatidiform mole.Genome Res2014
24234437ClinVar: public archive of relationships among sequence variation and human phenotype.Nucleic Acids Res2014
25373144Single haplotype assembly of the human genome from a hydatidiform mole.Genome Res2014
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Collaborators

Donna R Maglott
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 15
Kim D Pruitt
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 12
Michael DiCuccio
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 12
Evan E Eichler
University of Washington
Co-authored papers 12
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 10
Lynn M Schriml
University of Maryland School of Medicine, Institute for Genome Sciences
Co-authored papers 8
Wolfgang Helmberg
Medical University of Graz
Co-authored papers 8
Yuri Kapustin
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 8
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 8
Stephen H Bryant
National Center for Biotechnology Information
Co-authored papers 8
Tanya Barrett
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 8
Alexandre Souvorov
Co-authored papers 7
Richard K Wilson
The Ohio State University
Co-authored papers 7
Paul Flicek
European Bioinformatics Institute
Co-authored papers 7
Tina Graves
McDonnell Genome Institute, Washington University
Co-authored papers 7
Richa Agarwala
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 6
David B Jaffe
Co-authored papers 6
Ron Edgar
Co-authored papers 6
Michael Feolo
University of Massachusetts Medical School
Co-authored papers 5
Tim Hubbard
Co-authored papers 5
Richard Durbin
University of Cambridge
Co-authored papers 4
Ilene Karsch-Mizrachi
Co-authored papers 4
Justin Paschall
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 4
Eric S Lander
Vanderbilt-Ingram Cancer Center, Vanderbilt University
Co-authored papers 4
Michael C Zody
Broad Institute of Harvard and MIT
Co-authored papers 4
Paul A Kitts
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 4
James F Gusella
Co-authored papers 4
Mark S Guyer
National Human Genome Research Institute
Co-authored papers 4
Ze Cheng
University of Washington School of Medicine
Co-authored papers 4
Xinwei She
Rosetta Inpharmatics LLC
Co-authored papers 4
Release 1.2