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Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequenc...

Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequenc...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2329992511

Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair derived artifacts as residual errors

About this item

Full title

Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair derived artifacts as residual errors

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2019-12

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

To improve the accuracy and the cost-efficiency of next-generation sequencing in ultralow-frequency mutation detection, we developed the Paired-End and Complementary Consensus Sequencing (PECC-Seq), a PCR-free duplex consensus sequencing approach. PECC-Seq employed shear points as endogenous barcodes to identify consensus sequences from the overlap...

Alternative Titles

Full title

Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair derived artifacts as residual errors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2329992511

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2329992511

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/2019.12.22.886440