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Joe Meehan

Researcher at National Center for Toxicological Research

Publications -  11
Citations -  726

Joe Meehan is an academic researcher from National Center for Toxicological Research. The author has contributed to research in topics: Population & Microarray analysis techniques. The author has an hindex of 8, co-authored 11 publications receiving 625 citations. Previous affiliations of Joe Meehan include Food and Drug Administration.

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The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundance

TL;DR: RNA-seq outperforms microarray in DEG verification as assessed by quantitative PCR, with the gain mainly due to its improved accuracy for low-abundance transcripts, and classifiers to predict MOAs perform similarly when developed using data from either platform.
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An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq era

TL;DR: Signature genes of predictive models are reciprocally transferable between microarray andRNA-seq data for model development, and microarray-based models can accurately predict RNA-seq-profiled samples; while RNA-sequencing-based model are less accurate in predicting micro array-Profiled samples and are affected both by the choice of modeling algorithm and the gene mapping complexity.
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Whole genome sequencing of 35 individuals provides insights into the genetic architecture of Korean population

TL;DR: This study identified the SNVs that were found in the Korean population but not seen in other populations, and explored the corresponding genes and pathways as well as the associated disease terms and drug terms.

The MAQC-II Project: A comprehensive study of common practices for the development and validation of microarray-based predictive models.

Leming Shi, +196 more
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Alignment of Short Reads: A Crucial Step for Application of Next-Generation Sequencing Data in Precision Medicine

TL;DR: Current available alignment algorithms and their major strategies such as seed-and-extend and q-gram filter are reviewed and the challenges in current alignment algorithms are discussed, including alignment in multiple repeated regions, long reads alignment and alignment facilitated with known genetic variants.