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Justin T. Reese
Texas A&M University
35Publications
21H-index
5,657Citations
Publications 35
Newest
Published on Nov 17, 2017
Nathan Dunn8
Estimated H-index: 8
,
Colin Diesh4
Estimated H-index: 4
+ 17 AuthorsJustin T. Reese21
Estimated H-index: 21
Published on Jan 1, 2017
Nathan Dunn8
Estimated H-index: 8
,
Colin Diesh4
Estimated H-index: 4
+ 14 AuthorsJustin T. Reese21
Estimated H-index: 21
Published on Sep 1, 2016in Genomics data
Matthew R. Tarver5
Estimated H-index: 5
(ARS: Agricultural Research Service),
Qiang Huang5
Estimated H-index: 5
(University of Bern)
+ 5 AuthorsJay D. Evans62
Estimated H-index: 62
(ARS: Agricultural Research Service)
The small hive beetle (SHB), Aethina tumida, is a major pest of managed honey bee (Apis mellifera) colonies in the United States and Australia, and an emergent threat in Europe. While strong honey bee colonies generally keep SHB populations in check, weak or stressed colonies can succumb to infestations. This parasite has spread from a sub-Saharan Africa to three continents, leading to immense management and regulatory costs. We performed a transcriptomic analysis involving deep sequencing of mu...
Published on Aug 9, 2016
Nathan Dunn8
Estimated H-index: 8
,
Justin T. Reese21
Estimated H-index: 21
+ 12 AuthorsEric Rasche4
Estimated H-index: 4
Published on Jun 15, 2016
Nathan Dunn8
Estimated H-index: 8
,
Justin T. Reese21
Estimated H-index: 21
+ 11 AuthorsEric Rasche4
Estimated H-index: 4
Published on Jun 3, 2016
Nathan Dunn8
Estimated H-index: 8
,
Justin T. Reese21
Estimated H-index: 21
+ 11 AuthorsEric Rasche4
Estimated H-index: 4
Published on Dec 1, 2015in BMC Genomics3.50
Brandi L. Cantarel26
Estimated H-index: 26
(Baylor University),
Yunping Lei5
Estimated H-index: 5
(University of Texas at Austin)
+ 5 AuthorsRichard H. Finnell60
Estimated H-index: 60
(University of Texas at Austin)
Background Deidentified newborn screening bloodspot samples (NBS) represent a valuable potential resource for genomic research if impediments to whole exome sequencing of NBS deoxyribonucleic acid (DNA), including the small amount of genomic DNA in NBS material, can be overcome. For instance, genomic analysis of NBS could be used to define allele frequencies of disease-associated variants in local populations, or to conduct prospective or retrospective studies relating genomic variation to disea...
Published on May 1, 2014in Nature Communications11.88
Nicolas Terrapon13
Estimated H-index: 13
(AMU: Aix-Marseille University),
Cai Li19
Estimated H-index: 19
(UCPH: University of Copenhagen)
+ 40 AuthorsKaustubh Gokhale5
Estimated H-index: 5
(ASU: Arizona State University)
Although eusociality evolved independently within several orders of insects, research into the molecular underpinnings of the transition towards social complexity has been confined primarily to Hymenoptera (for example, ants and bees). Here we sequence the genome and stage-specific transcriptomes of the dampwood termite Zootermopsis nevadensis (Blattodea) and compare them with similar data for eusocial Hymenoptera, to better identify commonalities and differences in achieving this significant tr...
Published on Jan 1, 2014in BMC Genomics3.50
Christine G. Elsik25
Estimated H-index: 25
(MU: University of Missouri),
Kim C. Worley55
Estimated H-index: 55
(BCM: Baylor College of Medicine)
+ 45 AuthorsBart Devreese49
Estimated H-index: 49
(UGent: Ghent University)
Background: The first generation of genome sequence assemblies and annotations have had a significant impact upon our understanding of the biology of the sequenced species, the phylogenetic relationships among species, the study of populations within and across species, and have informed the biology of humans. As only a few Metazoan genomes are approaching finished quality (human, mouse, fly and worm), there is room for improvement of most genome assemblies. The honey bee (Apis mellifera) genome...
Published on Jan 1, 2014in BMC Bioinformatics2.51
Brandi L. Cantarel26
Estimated H-index: 26
(Baylor University),
Daniel Weaver8
Estimated H-index: 8
+ 3 AuthorsJustin T. Reese21
Estimated H-index: 21
Background Accurate genomic variant detection is an essential step in gleaning medically useful information from genome data. However, low concordance among variant-calling methods reduces confidence in the clinical validity of whole genome and exome sequence data, and confounds downstream analysis for applications in genome medicine. Here we describe BAYSIC (BAYeSian Integrated Caller), which combines SNP variant calls produced by different methods (e.g. GATK, FreeBayes, Atlas, SamTools, etc.) ...
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