Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Biotechnology
Link
http://link.springer.com/content/pdf/10.1186/s12864-016-3425-4.pdf
Reference26 articles.
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3. Schirmer M, Ijaz U, D’Amore R, Hall N, Sloan WT, Quince C. Insight into biases and sequencing errors for amplicon sequencing with the illumina miseq platform. Nucleic Acids Res. 2015; 43(6):e37.
4. Lou DI, Hussmann JA, McBee RM, Acevedo A, Andino R, Press WH, Sawyer SL. High-throughput dna sequencing errors are reduced by orders of magnitude using circle sequencing. Proc Natl Acad Sci. 2013; 110(49):19872–7. doi: 10.1073/pnas.1319590110 .
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