2022
Whole‐exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants
Olfson E, Lebowitz ER, Hommel G, Pashankar N, Silverman WK, Fernandez TV. Whole‐exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants. Depression And Anxiety 2022, 39: 474-484. PMID: 35312124, PMCID: PMC9246845, DOI: 10.1002/da.23251.Peer-Reviewed Original ResearchMeSH KeywordsAnxiety DisordersBiological ProductsExomeGenetic Predisposition to DiseaseHumansSequence Analysis, DNAConceptsWhole-exome DNA sequencingRisk genesDNA sequencingCanonical biological pathwaysMissense genetic variantsNovo variantsGenetic variant detectionParent-child triosGenomic approachesDe novo variantsLikely geneBiologic pathwaysDeleterious variantsBiological pathwaysDamaging variantsGenesGenetic variantsPathwayVariant detectionSequencingNetwork analysisGenetic factorsUnderlying biologyVariantsEnrichment
2008
Analysis of Insertional Sites of the SIRE1 Retroelement Family from Glycine Max Using GenBank BAC-end Sequences
Flasch DA, Rebman EK, Olfson EH, Nguyen KK, Geirut LE, Garland MC, Lindorfer CM, Laten HM. Analysis of Insertional Sites of the SIRE1 Retroelement Family from Glycine Max Using GenBank BAC-end Sequences. In Silico Biology 2008, 8: 531-543. PMID: 19374136, DOI: 10.3233/isb-00374.Peer-Reviewed Original ResearchMeSH KeywordsDatabases, Nucleic AcidDNA, IntergenicGlycineMultigene FamilyRetroelementsSequence Analysis, DNAConceptsRetroelement familiesGenome Survey Sequence databasesProtein-coding genesLow copy number sequencesClear consensus sequenceTy1/copia familyBAC end sequencesClass II transposable elementsSoybean genomeCopia familiesGenomic assembliesPlant membersSatellite DNATransposable elementsRepetitive elementsConsensus sequenceGlycine maxSequence databasesCopy numberReverse transcriptase geneInsertional siteGenomeGenesSIRE1Transcriptase gene