Benjamin Langmead
Molecular Biology · 2010–2012
A researcher in the Science corpus: 4 papers; trusts 16 researchers and is trusted by 17 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 50 citations into it; #2,964 of 17,773 by trust here, #4,050 by citations
- Genetics — 16 citations into it
- Artificial Intelligence — 6 citations into it
Whom Benjamin Langmead trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Ben Langmead
- Muthu Dayalan
- Mark D. Robinson
- John D. Storey
- Pierre Baldi
- John C. Marioni
- Michael C. Schatz
- James H. Bullard
- Steven L. Salzberg
- Ryan Lister
Who trusts Benjamin Langmead overall
- Ronald C. Taylor
- Kimberly R. Kukurba
- Davis J. McCarthy
- Alicia Oshlack
- Aisling O'Driscoll
- Manuel Garber
- Hao Wu
- Hao Feng
- Yongseok Park
- Stephen B. Montgomery
Papers from Benjamin Langmead's perspective
Ordered by how strongly the researchers Benjamin Langmead trusts endorse each paper. Same corpus, a different order for every researcher.
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (Genome Research)
- RNA-Seq: a revolutionary tool for transcriptomics (Nature reviews genetics)
- A scaling normalization method for differential expression analysis of RNA-seq data (Genome Biology)
- Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments (BMC Bioinformatics)
- Human DNA methylomes at base resolution show widespread epigenomic differences
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
Their papers
- Tackling the widespread and critical impact of batch effects in high-throughput data (2010) — 2,064 citations
- Cloud-scale RNA-sequencing differential expression analysis with Myrna (2010) — 346 citations
- BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions (2012) — 745 citations
- Increased methylation variation in epigenetic domains across cancer types (2011) — 1,095 citations