Michael C. Schatz
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Why Is Michael C. Schatz Influential?
(Suggest an Edit or Addition)Michael C. Schatz's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Evolution of genes and genomes on the Drosophila phylogeny (2007) (1992)
- The contribution of de novo coding mutations to autism spectrum disorder (2014) (1988)
- De Novo Gene Disruptions in Children on the Autistic Spectrum (2012) (1335)
- Phased diploid genome assembly with single-molecule real-time sequencing (2016) (1328)
- Genome Sequence of Aedes aegypti, a Major Arbovirus Vector (2007) (1110)
- A whole-genome assembly of the domestic cow, Bos taurus (2009) (1080)
- Big Data: Astronomical or Genomical? (2015) (1079)
- The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus) (2008) (1016)
- Hybrid error correction and de novo assembly of single-molecule sequencing reads (2012) (947)
- Accurate detection of complex structural variations using single molecule sequencing (2017) (910)
- GenomeScope: fast reference‐free genome profiling from short reads (2017) (813)
- Draft Genome Sequence of the Sexually Transmitted Pathogen Trichomonas vaginalis (2007) (739)
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) (706)
- GAGE: A critical evaluation of genome assemblies and assembly algorithms. (2012) (702)
- Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species (2013) (702)
- CloudBurst: highly sensitive read mapping with MapReduce (2009) (690)
- KBase: The United States Department of Energy Systems Biology Knowledgebase (2018) (659)
- Draft Genome of the Filarial Nematode Parasite Brugia malayi (2007) (639)
- The complete sequence of a human genome (2021) (622)
- Quake: quality-aware detection and correction of sequencing errors (2010) (610)
- Major Structural Differences and Novel Potential Virulence Mechanisms from the Genomes of Multiple Campylobacter Species (2005) (594)
- Assemblathon 1: a competitive assessment of de novo short read assembly methods. (2011) (542)
- Searching for SNPs with cloud computing (2009) (520)
- Assembly of large genomes using second-generation sequencing. (2010) (487)
- Multi-Platform Next-Generation Sequencing of the Domestic Turkey (Meleagris gallopavo): Genome Assembly and Analysis (2010) (418)
- The advantages of SMRT sequencing (2013) (409)
- The pineapple genome and the evolution of CAM photosynthesis (2015) (402)
- RaGOO: fast and accurate reference-guided scaffolding of draft genomes (2019) (359)
- Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome (2015) (346)
- Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. (2018) (344)
- GenomeScope 2.0 and Smudgeplot for reference-free profiling of polyploid genomes (2019) (342)
- High-throughput sequence alignment using Graphics Processing Units (2007) (338)
- Piercing the dark matter: bioinformatics of long-range sequencing and mapping (2018) (332)
- Cloud Computing and the DNA Data Race (2010) (303)
- Genome assembly forensics: finding the elusive mis-assembly (2008) (290)
- Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato (2020) (288)
- Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99A (2008) (286)
- Genome of the long-living sacred lotus (Nelumbo nucifera Gaertn.) (2013) (270)
- Insight into the evolution of the Solanaceae from the parental genomes of Petunia hybrida (2016) (258)
- Aluminum tolerance in maize is associated with higher MATE1 gene copy number (2013) (250)
- Assembly complexity of prokaryotic genomes using short reads (2010) (235)
- Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa, document novel gene space of aus and indica (2014) (229)
- Genomic Analyses of the Microsporidian Nosema ceranae, an Emergent Pathogen of Honey Bees (2009) (220)
- Assemblytics: a web analytics tool for the detection of variants from an assembly (2016) (211)
- Design patterns for efficient graph algorithms in MapReduce (2010) (195)
- Interactive analysis and assessment of single-cell copy-number variations (2015) (179)
- Current challenges in de novo plant genome sequencing and assembly (2012) (175)
- Two New Complete Genome Sequences Offer Insight into Host and Tissue Specificity of Plant Pathogenic Xanthomonas spp (2011) (173)
- A robust benchmark for detection of germline large deletions and insertions (2020) (171)
- Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding (2016) (159)
- Reducing INDEL calling errors in whole genome and exome sequencing data (2014) (157)
- The advantages of SMRT sequencing (2013) (155)
- Rate of meristem maturation determines inflorescence architecture in tomato (2011) (154)
- Complex microbiome underlying secondary and primary metabolism in the tunicate-Prochloron symbiosis (2011) (139)
- Extending reference assembly models (2015) (138)
- Accurate de novo and transmitted indel detection in exome-capture data using microassembly (2014) (133)
- Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score (2012) (126)
- Third-generation sequencing and the future of genomics (2016) (123)
- Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED (2020) (121)
- Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps (2008) (119)
- Genomic survey of the ectoparasitic mite Varroa destructor, a major pest of the honey bee Apis mellifera (2010) (119)
- Error correction and assembly complexity of single molecule sequencing reads (2014) (106)
- Optimizing data intensive GPGPU computations for DNA sequence alignment (2009) (105)
- Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line (2017) (104)
- SplitMEM: a graphical algorithm for pan-genome analysis with suffix skips (2014) (101)
- Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv . oryzae PXO 99 A (2008) (99)
- Hawkeye: an interactive visual analytics tool for genome assemblies (2007) (97)
- Indel variant analysis of short-read sequencing data with Scalpel (2015) (96)
- Reference quality assembly of the 3.5-Gb genome of Capsicum annuum from a single linked-read library (2017) (96)
- A multi-task convolutional deep neural network for variant calling in single molecule sequencing (2019) (92)
- Metassembler: merging and optimizing de novo genome assemblies (2015) (90)
- Complete genomic and epigenetic maps of human centromeres (2021) (90)
- Paragraph: a graph-based structural variant genotyper for short-read sequence data (2019) (88)
- High-coverage sequencing and annotated assemblies of the budgerigar genome (2014) (87)
- Genome and transcriptome of the regeneration-competent flatworm, Macrostomum lignano (2015) (79)
- Cultivation and Complete Genome Sequencing of Gloeobacter kilaueensis sp. nov., from a Lava Cave in Kīlauea Caldera, Hawai'i (2013) (76)
- The genetic and epigenetic landscape of the Arabidopsis centromeres (2021) (76)
- Revealing Biological Modules via Graph Summarization (2009) (70)
- Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius (2016) (70)
- Nelumbo nucifera [data set] (2013) (70)
- A complete reference genome improves analysis of human genetic variation (2021) (68)
- The DNA data deluge (2013) (67)
- Benchmarking challenging small variants with linked and long reads (2020) (63)
- The DOE Systems Biology Knowledgebase (KBase) (2016) (63)
- Assembly of the 373k gene space of the polyploid sugarcane genome reveals reservoirs of functional diversity in the world's leading biomass crop (2019) (62)
- Addressing confounding artifacts in reconstruction of gene co-expression networks (2018) (61)
- Accurate detection of de novo and transmitted indels within exome-capture data using micro-assembly (2014) (60)
- From telomere to telomere: the transcriptional and epigenetic state of human repeat elements (2021) (56)
- Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99A (2008) (56)
- Structure and evolution of a proviral locus of Glyptapanteles indiensis bracovirus (2007) (54)
- A robust benchmark for germline structural variant detection (2019) (54)
- Fast Exact String Matching on the GPU (2011) (53)
- Highly-accurate long-read sequencing improves variant detection and assembly of a human genome (2019) (52)
- Epigenetic Patterns in a Complete Human Genome (2021) (52)
- Hybrid assembly with long and short reads improves discovery of gene family expansions (2017) (52)
- The bracteatus pineapple genome and domestication of clonally propagated crops (2019) (52)
- Duplication of a domestication locus neutralized a cryptic variant that caused a breeding barrier in tomato (2019) (51)
- Rapid parallel genome indexing with MapReduce (2011) (51)
- Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma (2017) (51)
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing (2019) (50)
- Automated correction of genome sequence errors. (2004) (49)
- Automated assembly scaffolding elevates a new tomato system for high-throughput genome editing (2021) (49)
- Ribbon: Visualizing complex genome alignments and structural variation (2016) (48)
- Hawkeye and AMOS: visualizing and assessing the quality of genome assemblies (2013) (47)
- Nanopore sequencing meets epigenetics (2017) (47)
- Novel circular RNA NF1 acts as a molecular sponge, promoting gastric cancer by absorbing miR-16. (2019) (47)
- Complete telomere-to-telomere de novo assembly of the Plasmodium falciparum genome through long-read (>11 kb), single molecule, real-time sequencing (2016) (46)
- The Challenge of Small-Scale Repeats for Indel Discovery (2015) (46)
- Applying Rapid Whole-Genome Sequencing To Predict Phenotypic Antimicrobial Susceptibility Testing Results among Carbapenem-Resistant Klebsiella pneumoniae Clinical Isolates (2018) (45)
- Hypo-Osmotic-Like Stress Underlies General Cellular Defects of Aneuploidy (2019) (45)
- Parrot Genomes and the Evolution of Heightened Longevity and Cognition (2018) (43)
- The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2022 update (2022) (41)
- Genotyping in the Cloud with Crossbow (2012) (40)
- Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (2021) (39)
- The evolution of inflorescence diversity in the nightshades and heterochrony during meristem maturation (2016) (38)
- Semi-automated assembly of high-quality diploid human reference genomes (2022) (37)
- Biological data sciences in genome research (2015) (36)
- The complete sequence of a human Y chromosome (2022) (35)
- Scikit-ribo Enables Accurate Estimation and Robust Modeling of Translation Dynamics at Codon Resolution. (2018) (35)
- Ribbon: intuitive visualization for complex genomic variation (2020) (35)
- Antibiotic pressure on the acquisition and loss of antibiotic resistance genes in Klebsiella pneumoniae (2018) (32)
- Integrated Microbial Survey Analysis of Prokaryotic Communities for the PhyloChip Microarray (2010) (32)
- LRSim: A Linked-Reads Simulator Generating Insights for Better Genome Partitioning (2017) (32)
- BMC Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99 A (2008) (32)
- The rise of a digital immune system (2012) (31)
- Genomic diversity of SARS-CoV-2 during early introduction into the Baltimore–Washington metropolitan area (2021) (29)
- A multi-task convolutional deep neural network for variant calling in single molecule sequencing (2018) (28)
- Parliament2: Accurate structural variant calling at scale (2020) (26)
- Characterization of Insertion Sites in Rainbow Papaya, the First Commercialized Transgenic Fruit Crop (2008) (25)
- Conservation Genomics of the Declining North American Bumblebee Bombus terricola Reveals Inbreeding and Selection on Immune Genes (2018) (25)
- Dual functions of Macpiwi1 in transposon silencing and stem cell maintenance in the flatworm Macrostomum lignano (2015) (25)
- Teaser: Individualized benchmarking and optimization of read mapping results for NGS data (2015) (25)
- Computational thinking in the era of big data biology (2012) (24)
- TGF-β reduces DNA ds-break repair mechanisms to heighten genetic diversity and adaptability of CD44+/CD24− cancer cells (2017) (23)
- Jasmine: Population-scale structural variant comparison and analysis (2021) (22)
- Local adaptation and archaic introgression shape global diversity at human structural variant loci (2021) (21)
- The DNA Data Deluge: Fast, efficient genome sequencing machines are spewing out more data than geneticists can analyze. (2013) (19)
- Genomic Diversity of SARS-CoV-2 During Early Introduction into the United States National Capital Region (2020) (19)
- 16GT: a fast and sensitive variant caller using a 16-genotype probabilistic model (2017) (17)
- Clonal Hematopoiesis Before, During, and After Human Spaceflight (2020) (16)
- De novo genome assembly of Candida glabrata reveals cell wall protein complement and structure of dispersed tandem repeat arrays (2020) (16)
- The missing graphical user interface for genomics (2010) (15)
- Automated assembly scaffolding using RagTag elevates a new tomato system for high-throughput genome editing (2022) (15)
- A plasmid locus associated with Klebsiella clinical infections encodes a microbiome-dependent gut fitness factor (2020) (15)
- Pan-genomic matching statistics for targeted nanopore sequencing (2021) (14)
- Molecular genetic diversity and characterization of conjugation genes in the fish parasite Ichthyophthirius multifiliis. (2015) (14)
- Genome‐wide patterns of transposon proliferation in an evolutionary young hybrid fish (2019) (14)
- Precise detection of de novo single nucleotide variants in human genomes (2018) (13)
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) (13)
- Vargas: heuristic-free alignment for assessing linear and graph read aligners (2019) (12)
- Parallel Network Motif Finding (2007) (12)
- Assemblytics: a web analytics tool for the detection of assembly-based variants (2016) (12)
- iGenomics: Comprehensive DNA sequence analysis on your Smartphone (2020) (12)
- On Algorithmic Complexity of Biomolecular Sequence Assembly Problem (2014) (10)
- Minos: variant adjudication and joint genotyping of cohorts of bacterial genomes (2021) (10)
- Cell wall protein variation, break‐induced replication, and subtelomere dynamics in Candida glabrata (2021) (9)
- SplitThreader: Exploration and analysis of rearrangements in cancer genomes (2016) (9)
- High resolution copy number inference in cancer using short-molecule nanopore sequencing (2020) (9)
- Piercing the dark matter: bioinformatics of long-range sequencing and mapping (2018) (9)
- Correction: Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding (2016) (9)
- SVCollector: Optimized sample selection for validating and long-read resequencing of structural variants (2018) (8)
- Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L (2018) (8)
- The genomic basis of evolutionary differentiation among honey bees (2021) (8)
- Sapling: Accelerating Suffix Array Queries with Learned Data Models (2020) (8)
- Sixty years of genome biology (2013) (8)
- Phosphorylation of C-terminal polycystin-2 influences the interaction with PIGEA14: a QCM study based on solid supported membranes. (2013) (8)
- An anchored chromosome‐scale genome assembly of spinach improves annotation and reveals extensive gene rearrangements in euasterids (2021) (8)
- Skyhawk: An Artificial Neural Network-based discriminator for reviewing clinically significant genomic variants (2018) (7)
- The human origin recognition complex is essential for pre-RC assembly, mitosis, and maintenance of nuclear structure (2020) (7)
- Natural Genetic Diversity in Tomato Flavor Genes (2021) (7)
- First near complete haplotype phased genome assembly of River buffalo (Bubalus bubalis) (2019) (7)
- Interactive analysis and quality assessment of single-cell copy-number variations (2014) (7)
- Sapling: Accelerating Suffix Array Queries with Learned Data Models. (2020) (7)
- Silica precipitation by synthetic minicollagens. (2013) (7)
- Complete Sequence of a 641-kb Insertion of Mitochondrial DNA in the Arabidopsis thaliana Nuclear Genome (2022) (7)
- Erratum to: The advantages of SMRT sequencing (2017) (6)
- Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. (2018) (6)
- Multi-tissue integrative analysis of personal epigenomes (2021) (6)
- GenomeScope: Fast reference-free genome profiling from short reads (2016) (6)
- De novo identification of “ heterotigs ” towards accurate and in-phase assembly of complex plant genomes (2012) (5)
- High performance computing for dna sequence alignment and assembly (2010) (5)
- SNPC-1.3 is a sex-specific transcription factor that drives male piRNA expression in C. elegans (2020) (5)
- Title: A complete human reference genome improves variant calling for population and clinical genomics (2021) (4)
- Artificial Intelligence and Cardiovascular Genetics (2022) (4)
- Reducing INDEL calling errors in whole genome and exome sequencing data (2014) (4)
- Optimized sample selection for cost-efficient long-read population sequencing (2020) (4)
- Clonal hematopoiesis before, during, and after human spaceflight. (2021) (4)
- New whole genome de novo assemblies of three divergent strains of rice (O. sativa) documents novel gene space of aus and indica (2014) (4)
- The next 20 years of genome research (2015) (4)
- Recovering rearranged cancer chromosomes from karyotype graphs (2019) (4)
- Approaching complete genomes, transcriptomes and epi-omes with accurate long-read sequencing (2023) (4)
- TGF-b reduces DNA ds-break repair mechanisms to heighten genetic diversity and adaptability of CD 44 + / CD 24 � cancer cells (2017) (4)
- NanoBLASTer: Fast alignment and characterization of Oxford Nanopore single molecule sequencing reads (2016) (3)
- Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads (2019) (3)
- Management, Analyses, and Distribution of the MaizeCODE Data on the Cloud (2019) (3)
- Metassembler: merging and optimizing de novo genome assemblies (2015) (3)
- Answering the demands of digital genomics (2014) (3)
- Author Correction: Duplication of a domestication locus neutralized a cryptic variant that caused a breeding barrier in tomato (2019) (3)
- Using Galaxy to Perform Large‐Scale Interactive Data Analyses—An Update (2021) (3)
- Unraveling molecular mechanisms of immunity and cancer-resistance using the genomes of the Neotropical bats Artibeus jamaicensis and Pteronotus mesoamericanus (2020) (3)
- Scikit-ribo: Accurate estimation and robust modeling of translation dynamics at codon resolution (2017) (3)
- Reducing INDEL errors in whole-genome and exome sequencing (2014) (2)
- Genome of the long-living sacred lotus (Nelumbo nucifera Gaertn.) (2013) (2)
- In memory of James Taylor: the birth of Galaxy (2020) (2)
- Differences in activity and stability drive transposable element variation in tropical and temperate maize (2022) (2)
- A robust benchmark for detection of germline large deletions and insertions (2020) (2)
- SplitMEM: Graphical pan-genome analysis with suffix skips (2014) (2)
- Machine learning based prediction of gliomas with germline mutations obtained from whole exome sequences from TCGA and 1000 Genomes Project (2019) (2)
- Long-read sequencing reveals rapid evolution of immunity- and cancer-related genes in bats (2020) (2)
- A draft assembly and analysis of the highly heterozygous diploid red raspberry genome (Rubus idaeus cv. Heritage) (2012) (2)
- The bracteatus pineapple genome and domestication of clonally propagated crops (2019) (2)
- LRSim: a Linked Reads Simulator generating insights for better genome partitioning (2017) (2)
- LongTron: Automated Analysis of Long Read Spliced Alignment Accuracy (2020) (2)
- The DNA60IFX contest (2013) (2)
- Efforts to deregulate Rainbow papaya in Japan: Molecular characterization of transgene and vector inserts (2010) (2)
- The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models (2022) (2)
- Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L (2018) (1)
- Cross-species regulatory landscapes and elements revealed by novel joint systematic integration of human and mouse blood cell epigenomes (2023) (1)
- Modbamtools: Analysis of single-molecule epigenetic data for long-range profiling, heterogeneity, and clustering (2022) (1)
- Computational thinking in the era of big data biology (2012) (1)
- Current challenges in de novo plant genome sequencing and assembly (2012) (1)
- Minos: variant adjudication and joint genotyping of cohorts of bacterial genomes (2022) (1)
- Large-scale Sequencing and Assembly of Cereal Genomes Using Blacklight (2014) (1)
- Abstract A27: Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma (2016) (1)
- Samovar: Single-sample mosaic SNV calling with linked reads (2019) (1)
- Graph genomes article collection (2019) (1)
- Diversifying the genomic data science research community (2022) (1)
- Author Correction: A robust benchmark for detection of germline large deletions and insertions (2020) (1)
- Utility of long-read sequencing for All of Us (2023) (1)
- Jasmine and Iris: population-scale structural variant comparison and analysis (2023) (1)
- Democratizing long-read genome assembly. (2021) (1)
- Addressing confounding artifacts in reconstruction of gene co-expression networks (2019) (1)
- RaGOO: fast and accurate reference-guided scaffolding of draft genomes (2019) (1)
- Concerning the eXclusion in human genomics: The choice of sex chromosome representation in the human genome drastically affects number of identified variants (2023) (1)
- analysis Ribbon: intuitive visualization for complex genomic variation (2021) (1)
- Complete sequence of a 641-kb insertion of mitochondrial DNA in the Arabidopsis nuclear genome (2022) (0)
- A robust benchmark for germline large deletion and insertion detection (0)
- Bioinformatics of DNA [Scanning the Issue] (2017) (0)
- Quality-aware error correction of sequencing reads (2010) (0)
- Talk from Mike Schatz at the Cold Spring Harbor Laboratory In-House Symposium (2012) (2012) (0)
- Faculty Opinions recommendation of De novo assembly and genotyping of variants using colored de Bruijn graphs. (2012) (0)
- SciApps: A Cloud-Based Platform for Analyses and Distribution of the MaizeCODE data (2019) (0)
- Progress on the development of a genome sequence for red raspberry Rubus idaeus (2012) (0)
- tbenavi1/genomescope2.0: First Release of GenomeScope 2.0 (2020) (0)
- The curators' perspective (2013) (0)
- The curators' perspective (2013) (0)
- NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-Space: Reaching out to Clinicians. (2023) (0)
- Variation & RNAseq Service in KBase (2014) (0)
- Perfect Long Read Assembly and the Rise of Pan-Genomics (2015) (0)
- Same-Cell Co-Occurrence of RAS Hotspot and BRAF V600E Mutations in Treatment-Naive Colorectal Cancer (2022) (0)
- Erratum to: The advantages of SMRT sequencing (2017) (0)
- Xanthomonas spp. Specificity of Plant Pathogenic Offer Insight into Host and Tissue Two New Complete Genome Sequences (2011) (0)
- The Resurgence of Reference Quality Genomes (2016) (0)
- In memory of James Taylor: the birth of Galaxy (2020) (0)
- solutions: DNA60IFX Solutions (2015) (0)
- Author response: TGF-β reduces DNA ds-break repair mechanisms to heighten genetic diversity and adaptability of CD44+/CD24− cancer cells (2016) (0)
- Supplementary Material 24 (2010) (0)
- The DNA60IFX contest (2013) (0)
- Improving Genome Assembly without Sequencing (2005) (0)
- BEATRICE: Bayesian Fine-mapping from Summary Data using Deep Variational Inference (2023) (0)
- Sixty years of genome biology (2013) (0)
- Hypo-osmotic-like stress underlies general cellular defects of aneuploidy (2019) (0)
- Faculty Opinions recommendation of Detecting novel associations in large data sets. (2013) (0)
- Genome Assembly Analytics with Hawkeye (2006) (0)
- Extending reference assembly models (2015) (0)
- Establishing Physalis as a Solanaceae model system enables genetic reevaluation of the inflated calyx syndrome (2022) (0)
- Abstract 850: Comprehensive genome and transcriptome structural analysis of a breast cancer cell line using single molecule sequencing (2016) (0)
- Title 16 GT : A fast and sensitive variant caller using a 16-genotypeprobabilistic model (2017) (0)
- Casa del Dean. Mexicos Renaissance-Juwel in euem Licht (2013) (0)
- The advantages of SMRT sequencing (2013) (0)
- Structural Variation Analysis with Long Single Molecule Reads (2016) (0)
- Random Forest Factorization Reveals Latent Structure in Single Cell RNA Sequencing Data (2021) (0)
- Scikit-ribo Enables Accura te Estimation and Robust Modeling of Translation Dynamics at Codon Resolution Graphical (2018) (0)
- Wasp Polydnavirus Polymorphism (2006) (0)
- De novo assembly of complex genomes using 3rd generation sequencing (2012) (0)
- GenomeScope 2.0 and Smudgeplot for reference-free profiling of polyploid genomes (2020) (0)
- AIAA – 2004 – 1243 Separation Control by Self-Activated Movable Flaps (2004) (0)
- Author Correction: Duplication of a domestication locus neutralized a cryptic variant that caused a breeding barrier in tomato (2019) (0)
- Jaen Turner (Hg.): the Dictionary of Art (1999) (0)
- Multi-tissue integrative analysis of personal epigenomes [preprint] Multi-tissue integrative analysis of personal epigenomes [preprint] you. (2021) (0)
- Faculty Opinions recommendation of Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome. (2010) (0)
- Duplication of a domestication locus neutralized a cryptic variant that caused a breeding barrier in tomato (2019) (0)
- de novo Assembly of Complex Genomes Using Single Molecule Sequencing (2014) (0)
- A refined characterization of large-scale genomic differences in the first complete human genome (2022) (0)
- Geospatial Phylogenomics bed bugs in NYC-ncomms10164 (2016) (0)
- Fast and accurate genome-wide predictions and structural modeling of protein-protein interactions using Galaxy (2021) (0)
- Graph genomes article collection (2019) (0)
- Hybrid assembly with long and short reads improves discovery of gene family expansions (2017) (0)
- The Resurgence of Reference Quality Genome Sequence (2015) (0)
- Reference quality assembly of the 3.5-Gb genome of Capsicum annuum from a single linked-read library (2018) (0)
- The DNA 60 IFX contest (2013) (0)
- The advantages of SMRT sequencing (2013) (0)
- Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa, document novel gene space of aus and indica (2014) (0)
- Galaxy for protected datasets (2021) (0)
- Sketching and sampling approaches for fast and accurate long read classification (2021) (0)
- Teaser: Individualized benchmarking and optimization of read mapping results for NGS data (2015) (0)
- Entering the Era of Mega-genomics ( JGI Seventh Annual User Meeting 2012: Genomics of Energy and Environment) (2012) (0)
- A master regulator of regeneration (2019) (0)
- On the Transcriptomic Signature and General Stress State Associated with Aneuploidy (2020) (0)
- Illuminating the genetics of complex human diseases (2012) (0)
- Paragraph: a graph-based structural variant genotyper for short-read sequence data (2019) (0)
- Accurate detection of complex structural variations using single-molecule sequencing (2018) (0)
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What Schools Are Affiliated With Michael C. Schatz?
Michael C. Schatz is affiliated with the following schools:
- Virginia Tech
- University of Maryland, College Park
- University of Göttingen
- Stony Brook University
- Cold Spring Harbor Laboratory School of Biological Sciences
- University of Dundee
- University System of Maryland
- University of Glasgow
- Technical University of Denmark
- Imperial College London
- Newcastle University
- Carnegie Mellon University
- Johns Hopkins University
- University of Pittsburgh