Adrian Powell

Dr. Adrian Powell

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 November 2019 in The Plant Journal
Verified
Journal Article
Open access
PDF file
NFNoe Fernandez-Pozo
Noe Fernandez-Pozo
FHFabian Haas
Fabian Haas
RMRabea Meyberg
Rabea Meyberg
KUKristian K. Ullrich
Kristian K. Ullrich
MHManuel Hiss
Manuel Hiss
SRStefan Rensing
Stefan Rensing
Summary: Physcomitrella patens is a bryophyte model plant that is often used to study plant evolution and development. Its resources are of great importance for comparative genomics and evo‐devo approaches. However, expression data from Physcomitrella patens were so far generated using different gene annotation versions and three different platforms: CombiMatrix and NimbleGen expression microarrays and RNA sequencing. The currently available P. patens expression data are distributed across three tools with different visualization methods to access the data. Here, we introduce an interactive expression atlas, Physcomitrella Expression Atlas Tool (PEATmoss), that unifies publicly available expression data for P. patens and provides multiple visualization methods to query the data in a single web‐based tool. Moreover, PEATmoss includes 35 expression experiments not previously available in any other expression atlas. To facilitate gene expression queries across different gene annotation versions, and to access P. patens annotations and related resources, a lookup database and web tool linked to PEATmoss was implemented. PEATmoss can be accessed at https://peatmoss.online.uni-marburg.de

6 April 2022 in G3: Genes, Genomes, Genetics
Verified
Journal Article
Open access
PDF file
NMNicolas Morales
Nicolas Morales
AOAlex C Ogbonna
Alex C Ogbonna
BEBryan J Ellerbrock
Bryan J Ellerbrock
GBGuillaume Bauchet
Guillaume Bauchet
TTTitima Tantikanjana
Titima Tantikanjana
Lukas MuellerLukas Mueller
Lukas Mueller
Modern breeding methods integrate next-generation sequencing and phenomics to identify plants with the best characteristics and greatest genetic merit for use as parents in subsequent breeding cycles to ultimately create improved cultivars able to sustain high adoption rates by farmers. This data-driven approach hinges on strong foundations in data management, quality control, and analytics. Of crucial importance is a central database able to (1) track breeding materials, (2) store experimental evaluations, (3) record phenotypic measurements using consistent ontologies, (4) store genotypic information, and (5) implement algorithms for analysis, prediction, and selection decisions. Because of the complexity of the breeding process, breeding databases also tend to be complex, difficult, and expensive to implement and maintain. Here, we present a breeding database system, Breedbase (https://breedbase.org/, last accessed 4/18/2022). Originally initiated as Cassavabase (https://cassavabase.org/, last accessed 4/18/2022) with the NextGen Cassava project (https://www.nextgencassava.org/, last accessed 4/18/2022), and later developed into a crop-agnostic system, it is presently used by dozens of different crops and projects. The system is web based and is available as open source software. It is available on GitHub (https://github.com/solgenomics/, last accessed 4/18/2022) and packaged in a Docker image for deployment (https://hub.docker.com/u/breedbase, last accessed 4/18/2022). The Breedbase system enables breeding programs to better manage and leverage their data for decision making within a fully integrated digital ecosystem.

1 March 2013 in Plant Physiology and Biochemistry
Verified
Journal Article
Closed access
APAdrian Powell
Adrian Powell
APAndrea R. Paleczny
Andrea R. Paleczny
HOHenry Olechowski
Henry Olechowski
R.J. Neil EmeryR.J. Neil Emery
R.J. Neil Emery

18 January 2021 in The Plant Journal
Verified
Journal Article
Closed access
PDF file
ARAnnett Richter
Annett Richter
APAdrian Powell
Adrian Powell
MMMahdieh Mirzaei
Mahdieh Mirzaei
LWLucy J. Wang
Lucy J. Wang
NMNavid Movahed
Navid Movahed
GJGeorg Jander
Georg Jander

18 May 2022 in The Plant Journal
Verified
Journal Article
Open access
APAdrian Powell
Adrian Powell
AFAri Feder
Ari Feder
JLJie Li
Jie Li
MSMaximilian H.‐W. Schmidt
Maximilian H.‐W. Schmidt
LCLance Courtney
Lance Courtney
BUBjörn Usadel
Björn Usadel
SUMMARY: Wild relatives of tomato are a valuable source of natural variation in tomato breeding, as many can be hybridized to the cultivated species (Solanum lycopersicum). Several, including Solanum lycopersicoides, have been crossed to S. lycopersicum for the development of ordered introgression lines (ILs), facilitating breeding for desirable traits. Despite the utility of these wild relatives and their associated ILs, few finished genome sequences have been produced to aid genetic and genomic studies. Here we report a chromosome‐scale genome assembly for S. lycopersicoides LA2951, which contains 37 938 predicted protein‐coding genes. With the aid of this genome assembly, we have precisely delimited the boundaries of the S. lycopersicoides introgressions in a set of S. lycopersicum cv. VF36 × LA2951 ILs. We demonstrate the usefulness of the LA2951 genome by identifying several quantitative trait loci for phenolics and carotenoids, including underlying candidate genes, and by investigating the genome organization and immunity‐associated function of the clustered Pto gene family. In addition, syntenic analysis of R2R3MYB genes sheds light on the identity of the Aubergine locus underlying anthocyanin production. The genome sequence and IL map provide valuable resources for studying fruit nutrient/quality traits, pathogen resistance, and environmental stress tolerance. We present a new genome resource for the wild species S. lycopersicoides, which we use to shed light on the Aubergine locus responsible for anthocyanin production. We also provide IL boundary mappings, which facilitated identifying novel carotenoid quantitative trait loci of which one was likely driven by an uncharacterized lycopene β‐cyclase whose function we demonstrate.