Michael C. Schatz

Michael C. Schatz's AcademicInfluence.com Rankings

Michael C. Schatz

Computer Science

#6750

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#7114

Historical Rank

Database

#3835

World Rank

#3990

Historical Rank

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Computer Science

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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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