Kasper D. Hansen
Molecular Biology · 2010–2017
A researcher in the Science corpus: 9 papers; trusts 45 researchers and is trusted by 62 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 132 citations into it; #492 of 17,773 by trust here, #2,498 by citations
- Genetics — 28 citations into it
- Artificial Intelligence — 12 citations into it
- Cancer Research — 11 citations into it
Whom Kasper D. Hansen trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Ben Langmead
- Maqc Consortium
- Mark D. Robinson
- Cole Trapnell
- Steven L. Salzberg
- Ali Mortazavi
- Ryan Lister
- Felix Krueger
- Yuanxin Xi
- Gordon K. Smyth
Who trusts Kasper D. Hansen overall
- Davis J. McCarthy
- Davide Risso
- Yunshun Chen
- Hao Wu
- Bo Li
- Simon Anders
- Hao Feng
- Yongseok Park
- Gordon K. Smyth
- Adam Roberts
Papers from Kasper D. Hansen's perspective
Ordered by how strongly the researchers Kasper D. Hansen trusts endorse each paper. Same corpus, a different order for every researcher.
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- RNA-Seq: a revolutionary tool for transcriptomics (Nature reviews genetics)
- Substantial biases in ultra-short read data sets from high-throughput DNA sequencing (Nucleic Acids Research)
- Human DNA methylomes at base resolution show widespread epigenomic differences
- A scaling normalization method for differential expression analysis of RNA-seq data (Genome Biology)
- Base-calling of automated sequencer traces using phred. II. Error probabilities.
- Highly integrated single-base resolution maps of the epigenome in Arabidopsis. (Cell)
- Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments (Statistical Applications in Genetics and Molecular Biology)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
Their papers
- Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments (2010) — 1,760 citations
- Biases in Illumina transcriptome sequencing caused by random hexamer priming (2010) — 722 citations
- Removing technical variability in RNA-seq data using conditional quantile normalization (2012) — 639 citations
- Cloud-scale RNA-sequencing differential expression analysis with Myrna (2010) — 346 citations
- Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays (2014) — 3,850 citations
- BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions (2012) — 745 citations
- Reproducible RNA-seq analysis using recount2 (2017) — 368 citations
- Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi (2016) — 764 citations
- Orchestrating high-throughput genomic analysis with Bioconductor (2015) — 3,336 citations