Steven J. M. Jones
Molecular Biology · 2003–2020
A researcher in the Science corpus: 44 papers; trusts 8 researchers and is trusted by 20 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 769 citations into it; #2,334 of 17,773 by trust here, #248 by citations
- Genetics — 364 citations into it
- Plant Science — 51 citations into it
- Computational Biology & Bioinformatics — 44 citations into it
- Ecology — 14 citations into it
- Statistical and Nonlinear Physics — 9 citations into it
Whom Steven J. M. Jones trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Steven J. M. Jones overall
- Daniel R. Zerbino
- Nicolas Dierckxsens
- Mihai Pop
- Mark J. P. Chaisson
- Marten Boetzer
- S. Deschamps
- Jay Shendure
Papers from Steven J. M. Jones's perspective
Ordered by how strongly the researchers Steven J. M. Jones trusts endorse each paper. Same corpus, a different order for every researcher.
- KEGG: Kyoto Encyclopedia of Genes and Genomes (Nucleic Acids Res.)
- Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models (Human Mutation)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Assembling millions of short DNA sequences using SSAKE (Bioinform.)
- COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
- Detection of large-scale variation in the human genome (Nature Genetics)
- Identification of common molecular subsequences.
- ABySS: a parallel assembler for short read sequence data. (Genome Research)
- De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer. (Genome Research)
- Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer (Nature)
Their papers
- ABySS: a parallel assembler for short read sequence data. (2009) — 1,394 citations
- Assembling millions of short DNA sequences using SSAKE (2006) — 546 citations
- De novo assembly and analysis of RNA-seq data (2010) — 993 citations
- Circos: an information aesthetic for comparative genomics. (2009) — 10,071 citations
- De novo transcriptome assembly with ABySS (2009) — 430 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
- Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients (2018) — 792 citations
- The genetic landscape of high-risk neuroblastoma (2013) — 1,115 citations
- Frequent mutation of histone modifying genes in non-Hodgkin lymphoma (2011) — 1,628 citations
- Molecular profiling reveals biologically discrete subsets and pathways of progression in diffuse glioma (2016) — 1,926 citations
- Comprehensive molecular profiling of lung adenocarcinoma (2014) — 5,176 citations
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) — 2,007 citations
- The whole-genome landscape of medulloblastoma subtypes (2017) — 956 citations
- Mutational Analysis Reveals the Origin and Therapy-driven Evolution of Recurrent Glioma (2013) — 1,210 citations
- Genomic Classification of Cutaneous Melanoma (2015) — 2,764 citations
- Assembling the 20 Gb white spruce (Picea glauca) genome from whole-genome shotgun sequencing data (2013) — 357 citations
- CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer (2017) — 582 citations
- Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma (2017) — 2,216 citations
- Integrated Genomic Characterization of Papillary Thyroid Carcinoma (2014) — 2,692 citations