Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis
Author(s) -
Jeppe Dyrberg Andersen,
Vânia Pereira,
Carlotta Pietroni,
Martin Mikkelsen,
Peter Johansen,
Claus Børsting,
Niels Morling
Publication year - 2014
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000114200
Subject(s) - biology , amplicon , barcode , fragment (logic) , computational biology , endonuclease , restriction enzyme , dna sequencing , amplicon sequencing , genetics , genomic library , sequencing by ligation , polymerase chain reaction , dna , gene , base sequence , computer science , 16s ribosomal rna , programming language , operating system
The simultaneous sequencing of samples from multiple individuals increases the efficiency of next-generation sequencing (NGS) while also reducing costs. Here we describe a novel and simple approach for sequencing DNA from multiple individuals per barcode. Our strategy relies on the endonuclease digestion of PCR amplicons prior to library preparation, creating a specific fragment pattern for each individual that can be resolved after sequencing. By using both barcodes and restriction fragment patterns, we demonstrate the ability to sequence the human melanocortin 1 receptor (MC1R) genes from 72 individuals using only 24 barcoded libraries.
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