What is he best known for?
The fields of study he is best known for:
His main research concerns Genome, Genetics, Computational biology, Sequence assembly and Genomics.
Much of his study explores Genome relationship to DNA sequencing.
In the subject of general Genetics, his work in Gene, Exome sequencing and Orthologous Gene is often linked to Single molecule real time sequencing and Anopheles, thereby combining diverse domains of study.
His Computational biology research incorporates themes from Short read, Human genome and Structural variant.
His Sequence assembly research is multidisciplinary, incorporating perspectives in Genome project, Hybrid genome assembly, Shotgun sequencing, Reference genome and Sequence.
His work deals with themes such as Ananas, Botany and Gene duplication, Neofunctionalization, which intersect with Genomics.
His most cited work include:
- Evolution of genes and genomes on the Drosophila phylogeny. (1731 citations)
- The contribution of de novo coding mutations to autism spectrum disorder (1436 citations)
- De Novo Gene Disruptions in Children on the Autistic Spectrum (1097 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Genome, Computational biology, Genetics, Genomics and Sequence assembly.
His Genome research is multidisciplinary, incorporating elements of Evolutionary biology and DNA sequencing.
His Computational biology research integrates issues from Human genome, Contig, Copy-number variation, Nanopore sequencing and Benchmark.
His work in Hybrid genome assembly, Exome sequencing, Locus, Comparative genomics and Shotgun sequencing is related to Genetics.
His research in Genomics intersects with topics in Algorithm, Short read, DNA and Artificial intelligence.
His Sequence assembly study combines topics from a wide range of disciplines, such as Structural variation, Theoretical computer science, Genome size, Ploidy and Haplotype.
He most often published in these fields:
- Genome (76.35%)
- Computational biology (64.53%)
- Genetics (35.47%)
What were the highlights of his more recent work (between 2019-2021)?
- Genome (76.35%)
- Computational biology (64.53%)
- Nanopore sequencing (14.53%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Genome, Computational biology, Nanopore sequencing, Evolutionary biology and Gene.
His Genome study incorporates themes from Phylogenetics, Sequence analysis and Benchmark.
His study in Computational biology is interdisciplinary in nature, drawing from both Human genome, Genetic diversity, Reference genome, Sequence assembly and Ploidy.
The study incorporates disciplines such as Mixture model, Polyploid, Loss of heterozygosity and Genome size in addition to Sequence assembly.
His Nanopore sequencing study combines topics in areas such as RNA and Nanopore.
His Chromosomal rearrangement research is within the category of Genetics.
Between 2019 and 2021, his most popular works were:
- Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato. (63 citations)
- Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato. (63 citations)
- GenomeScope 2.0 and Smudgeplot for reference-free profiling of polyploid genomes. (60 citations)
In his most recent research, the most cited papers focused on:
Michael C. Schatz mainly investigates Computational biology, Genome, Reference genome, Nanopore sequencing and Copy-number variation.
In his works, Michael C. Schatz conducts interdisciplinary research on Computational biology and Set.
His research in Genome intersects with topics in Evolutionary biology, Phylogenetics, Clade, Benchmark and Ploidy.
His Reference genome study also includes
- Metagenomics that intertwine with fields like Real time mapping and Illumina dye sequencing,
- Human genome together with Haplotype, Major histocompatibility complex and Contig.
His research integrates issues of Structural variation, Segmental duplication and Indel in his study of Copy-number variation.
His Cancer study contributes to a more complete understanding of Genetics.
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