Daniel C. Koboldt
Molecular Biology · 2007–2020
A researcher in the Science corpus: 27 papers; trusts 57 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 334 citations into it; #15,067 of 17,773 by trust here, #100 by citations
- Genetics — 269 citations into it; #5,571 of 6,854 by trust here, #25 by citations
- Cancer Research — 131 citations into it; #1,335 of 1,780 by trust here, #21 by citations
- Pathology and Forensic Medicine — 54 citations into it
- Pulmonary and Respiratory Medicine — 38 citations into it
- Artificial Intelligence — 22 citations into it
- Spectroscopy — 6 citations into it
Whom Daniel C. Koboldt trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Justin M. Zook
- Erik P. Garrison
- Daehwan Kim
- Konstantin Okonechnikov
- Ryan M. Layer
- Steven L. Salzberg
- James T. Robinson
- Tobias Rausch
- Jarupon Fah Sathirapongsasuti
Who trusts Daniel C. Koboldt overall
- Jerzy K. Kulski
- Jasreet Hundal
- Todd J. Treangen
- R. Ekblom
- M. Roach
- A. Young
- Niko Beerenwinkel
- B. Carreno
- T. Davoli
- Min Zhao
Papers from Daniel C. Koboldt's perspective
Ordered by how strongly the researchers Daniel C. Koboldt trusts endorse each paper. Same corpus, a different order for every researcher.
- Exome sequencing as a tool for Mendelian disease gene discovery
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- The Human Gene Mutation Database: 2008 update
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- A method and server for predicting damaging missense mutations
- Mapping copy number variation by population scale genome sequencing (Nature)
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing (Nature Genetics)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome (2009) — 2,302 citations
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples (2009) — 1,343 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012) — 4,654 citations
- Comprehensive molecular portraits of human breast tumors (2012) — 7,518 citations
- Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (2011) — 594 citations
- The origin and evolution of mutations in Acute Myeloid Leukemia (2012) — 1,580 citations
- MuSiC: Identifying mutational significance in cancer genomes (2012) — 667 citations
- Integrated Genomic Analyses of Ovarian Carcinoma (2011) — 7,559 citations
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) — 7,050 citations
- Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia (2013) — 4,584 citations
- The Next-Generation Sequencing Revolution and Its Impact on Genomics (2013) — 978 citations
- Best practices for variant calling in clinical sequencing (2020) — 322 citations
- Cancer Exome Analysis Reveals a T Cell Dependent Mechanism of Cancer Immunoediting (2012) — 1,252 citations
- Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing (2012) — 2,069 citations
- Whole Genome Analysis Informs Breast Cancer Response to Aromatase Inhibition (2012) — 1,068 citations
- Clonal Architecture of Secondary Acute Myeloid Leukemia (2012) — 794 citations