Michael F. Lawrence
Molecular Biology · 2009–2014
A researcher in the Science corpus: 5 papers; trusts 8 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 29 citations into it; #12,255 of 17,773 by trust here, #6,338 by citations
- Genetics — 15 citations into it; #4,379 of 6,854 by trust here, #4,743 by citations
- Cancer Research — 6 citations into it
Whom Michael F. Lawrence trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Michael F. Lawrence overall
- Michael I. Love
- Francis Blokzijl
- Manu N. Setty
- Raymond G. Cavalcante
- Wolfgang Huber
- Guangchuang Yu
- Jens Keilwagen
- Valerie Obenchain
- Altuna Akalin
- Timothy J. Peters
Papers from Michael F. Lawrence's perspective
Ordered by how strongly the researchers Michael F. Lawrence trusts endorse each paper. Same corpus, a different order for every researcher.
- Fast and SNP-tolerant detection of complex variants and splicing in short reads (Bioinform.)
- The generic genome browser: a building block for a model organism system database. (Genome Research)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Software for Computing and Annotating Genomic Ranges (PLoS Comput. Biol.)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- Circular genome visualization and exploration using CGView (Bioinform.)
- Sequence-specific error profile of Illumina sequencers (Nucleic Acids Research)
- ShortRead: a bioconductor package for input, quality assessment and exploration of high-throughput sequence data (Bioinform.)
- Introduction to algorithms
- Detecting differential usage of exons from RNA-seq data (Genome Research)
Their papers
- Software for Computing and Annotating Genomic Ranges (2013) — 4,046 citations
- Statistical inference for exploratory data analysis and model diagnostics (2009) — 170 citations
- ggbio: an R package for extending the grammar of graphics for genomic data (2012) — 299 citations
- VariantAnnotation: a Bioconductor package for exploration and annotation of genetic variants (2014) — 342 citations
- SomaticSignatures: inferring mutational signatures from single-nucleotide variants (2014) — 304 citations