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Andrew Anand Brown

dblp:125/8401 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2017
0000-0002-8087-3033ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome-wide association study
0.212016
Fast and efficient QTL mapper for thousands of molecular phenotypes · Bioinform. 2016
Bioinformatics and computational biology › statistical genetics
quantitative trait locus mapping
0.212016
Fast and efficient QTL mapper for thousands of molecular phenotypes · Bioinform. 2016
Bioinformatics and computational biology › gene regulation
cis-regulation
0.112017
veqtl-mapper: variance association mapping for molecular phenotypes · Bioinform. 2017
Bioinformatics and computational biology
gene expression analysis
0.112017
veqtl-mapper: variance association mapping for molecular phenotypes · Bioinform. 2017

Methods — techniques the papers use, named apart from their topics

variance QTL mapping · 0.3additive model · 0.3permutation procedure · 0.2beta distribution modeling · 0.2
YearPublicationVenuePosition
2017 veqtl-mapper: variance association mapping for molecular phenotypes
abstract
MOTIVATION: Genetic loci associated with the variance of phenotypic traits have been of recent interest as they can be signatures of genetic interactions, gene by environment interactions, parent of origin effects and canalization. We present a fast efficient tool to map loci affecting variance of gene expression and other molecular phenotypes in cis. Results: Applied to the publicly available Geuvadis gene expression dataset, we identify 816 loci associated with variance of gene expression using an additive model, and 32 showing differences in variance between homozygous and heterozygous alleles, signatures of parent of origin effects. AVAILABILITY AND IMPLEMENTATION: Documentation and links to source code and binaries for linux can be found at https://funpopgen.github.io/veqm/ . CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Andrew Anand Brown
Bioinform.1
2016 Fast and efficient QTL mapper for thousands of molecular phenotypes
abstract
MOTIVATION: In order to discover quantitative trait loci, multi-dimensional genomic datasets combining DNA-seq and ChiP-/RNA-seq require methods that rapidly correlate tens of thousands of molecular phenotypes with millions of genetic variants while appropriately controlling for multiple testing. RESULTS: We have developed FastQTL, a method that implements a popular cis-QTL mapping strategy in a user- and cluster-friendly tool. FastQTL also proposes an efficient permutation procedure to control for multiple testing. The outcome of permutations is modeled using beta distributions trained from a few permutations and from which adjusted P-values can be estimated at any level of significance with little computational cost. The Geuvadis & GTEx pilot datasets can be now easily analyzed an order of magnitude faster than previous approaches. AVAILABILITY AND IMPLEMENTATION: Source code, binaries and comprehensive documentation of FastQTL are freely available to download at http://fastqtl.sourceforge.net/ CONTACT: [email protected] or [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Halit Ongen, Alfonso Buil, Andrew Anand Brown, Emmanouil T. Dermitzakis, Olivier Delaneau
Bioinform.3