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Amplicon sequence variants and bias with Benjamin Callahan — the bioinformatics chat, a podcast about bioinformatics
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Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies - The Lancet Neurology
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Exact sequence variants should replace operational taxonomic units in marker-gene data analysis | The ISME Journal
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HGVS Recommendations for the Description of Sequence Variants: 2016 Update - Dunnen - 2016 - Human Mutation - Wiley Online Library
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Building an Indigenous Background Variant Library (IBVL) in Canada (Activity 3) | BC Children's Hospital Research Institute
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Variant Classification using ACMG/AMP Interpreting Sequence Guidelines - ClinGen | Clinical Genome Resource
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Quantifying the contribution of sequence variants with regulatory and evolutionary significance to 34 bovine complex traits | PNAS
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HGVS Recommendations for the Description of Sequence Variants: 2016 Update - Dunnen - 2016 - Human Mutation - Wiley Online Library
Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing | PLOS ONE
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Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls - Munich Cluster for Systems Neurology - LMU Munich
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a Venn diagram based on the Amplicon Sequence Variants (ASVs) observed... | Download Scientific Diagram
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