Abstract
Using a partial transcriptome of the snakelocks anemone (Anemonia sulcata) we identify toxin gene candidates that were incorrectly assembled into several Trinity components. Our approach recovers hidden diversity found within some toxin gene families that would otherwise go undetected when using Trinity, a widely used program for venom-focused transcriptome reconstructions. Unidentified hidden transcripts may significantly impact conclusions made regarding venom composition (or other multi-copy conserved genes) when using Trinity or other de novo assembly programs.
Keywords:
Next generation sequencing; Sea anemone venom; Sodium channel toxins; Trinity.
Copyright © 2015 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Gene Dosage
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Gene Expression Profiling / methods*
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Genetic Variation
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High-Throughput Nucleotide Sequencing
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Likelihood Functions
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Marine Toxins / chemistry*
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Marine Toxins / genetics
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Molecular Sequence Data
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Phylogeny
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Sea Anemones / genetics*
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Sequence Alignment
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Software
Associated data
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