Andrew Kasarskis
Molecular Biology · 2000–2017
A researcher in the Science corpus: 10 papers; trusts 5 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 100 citations into it; #5,001 of 17,773 by trust here, #283 by citations
- Genetics — 45 citations into it
- Plant Science — 11 citations into it
- Ecology — 7 citations into it
Whom Andrew Kasarskis trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Andrew Kasarskis overall
Papers from Andrew Kasarskis's perspective
Ordered by how strongly the researchers Andrew Kasarskis trusts endorse each paper. Same corpus, a different order for every researcher.
- An Eulerian path approach to DNA fragment assembly (Proceedings of the National Academy of Sciences of the United States of America)
- SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. (Genome Research)
- De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer. (Genome Research)
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- ALLPATHS: de novo assembly of whole-genome shotgun microreads. (Genome Research)
- Short read fragment assembly of bacterial genomes. (Genome Research)
- Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- ABySS: a parallel assembler for short read sequence data. (Genome Research)
- The diploid genome sequence of an Asian individual (Nature)
Their papers
- Gene Ontology: tool for the unification of biology (2000) — 42,547 citations
- The Stanford Microarray Database (2001) — 566 citations
- A window into third-generation sequencing. (2010) — 927 citations
- The Origin of the Haitian Cholera Outbreak Strain (2010) — 723 citations
- Sex-Specific Transcriptional Signatures in Human Depression (2017) — 678 citations
- Assuring the quality of next-generation sequencing in clinical laboratory practice (2012) — 463 citations
- Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia (2012) — 732 citations
- Origins of the E. coli Strain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany (2011) — 862 citations
- Mapping the Genetic Architecture of Gene Expression in Human Liver (2008) — 1,063 citations
- The Gene Ontology Consortium (2000) — 623 citations