2019
DOI: 10.1002/ece3.4981
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Identifying hybrids & the genomics of hybridization: Mallards & American black ducks of Eastern North America

Abstract: Resolving evolutionary relationships and establishing population structure depends on molecular diagnosability that is often limited for closely related taxa. Here, we use 3,200 ddRAD‐seq loci across 290 mallards, American black ducks, and putative hybrids to establish population structure and estimate hybridization rates. We test between traditional assignment probability and accumulated recombination events based analyses to assign hybrids to generational classes. For hybrid identification, we report the dis… Show more

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Cited by 45 publications
(115 citation statements)
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References 95 publications
(166 reference statements)
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“…Raw Illumina reads have been deposited in NCBI's Sequence Read Archive (SRA; http://www.ncbi.nlm.nih.gov/sra; SRA data PRJNA591912). We included sequenced mallard samples from Lavretsky, Janzen, et al () that were genetically characterized as either “Pure Western Mallard,” “Pure Non‐Western Mallard” or hybrids of the two ( N = 104; NCBI's SRA data PRJNA516035: see Table for BioSample Accession Numbers). These latter samples were from birds harvested by hunters in the wild.…”
Section: Methodsmentioning
confidence: 99%
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“…Raw Illumina reads have been deposited in NCBI's Sequence Read Archive (SRA; http://www.ncbi.nlm.nih.gov/sra; SRA data PRJNA591912). We included sequenced mallard samples from Lavretsky, Janzen, et al () that were genetically characterized as either “Pure Western Mallard,” “Pure Non‐Western Mallard” or hybrids of the two ( N = 104; NCBI's SRA data PRJNA516035: see Table for BioSample Accession Numbers). These latter samples were from birds harvested by hunters in the wild.…”
Section: Methodsmentioning
confidence: 99%
“…Processing of raw Illumina reads followed the computational pipeline described by DaCosta and Sorenson (; Python scripts available at http://github.com/BU-RAD-seq/ddRAD-seq-Pipeline) and following the steps outlined in Lavretsky, Janzen, et al (). Final output files (e.g., FASTA, ADMIXTURE, fineRADstructure ) were generated with custom python scripts (Lavretsky et al, ), in which alleles were scored as missing if they had less than 5× coverage.…”
Section: Methodsmentioning
confidence: 99%
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“…All sequences have been submitted to GenBank (accession numbers ‐ and –). In addition to new sequences, 40 previously published sequences were also used (accession numbers –, Fowler et al, ; & , Lavretsky et al ; & , Peters et al ; –, Lavretsky, Engilis, Eadie, & Peters ; and –, Lavretsky, Janzen, & McKracken ; –, –, Lavretsky, Engilis, Eadie, & Peters, ). Sequences were cut to the 303 bp present in all samples, which included the hypervariable region.…”
Section: Methodsmentioning
confidence: 99%