Tim Fennell
Molecular Biology · 2008–2017
A researcher in the Science corpus: 23 papers; trusts 1 researcher and is trusted by 13 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 313 citations into it; #4,448 of 17,773 by trust here, #81 by citations
- Ecology — 5 citations into it
Whom Tim Fennell trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Tim Fennell overall
Papers from Tim Fennell's perspective
Ordered by how strongly the researchers Tim Fennell trusts endorse each paper. Same corpus, a different order for every researcher.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- The human genome browser at UCSC.
- Identification of common molecular subsequences.
- Real-time DNA sequencing from single polymerase molecules. (Methods in Enzymology)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Next-generation DNA sequencing methods. (Annual review of genomics and human genetics (Print))
- Fast and accurate long-read alignment with Burrows–Wheeler transform (Bioinform.)
- Variation in genome-wide mutation rates within and between human families (Nature Genetics)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
Their papers
- The Sequence Alignment/Map format and SAMtools (2009) — 56,954 citations
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011) — 11,249 citations
- Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries (2011) — 1,169 citations
- Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing (2009) — 1,475 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
- Melanoma genome sequencing reveals frequent PREX2 mutations (2012) — 752 citations
- A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 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
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts (2009) — 4,613 citations
- Genomic Classification of Cutaneous Melanoma (2015) — 2,764 citations
- Integrated Genomic Characterization of Papillary Thyroid Carcinoma (2014) — 2,692 citations
- Scaling accurate genetic variant discovery to tens of thousands of samples (2017) — 1,758 citations
- Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas (2015) — 2,738 citations
- Association of a Low-Frequency Variant in HNF1A With Type 2 Diabetes in a Latino Population (2014) — 242 citations
- Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico (2013) — 472 citations
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
- Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease (2011) — 813 citations