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Understanding the structure of sequenced fragments from genomics libraries is essential for accurate read preprocessing. Currently, different assays and sequencing technologies require custom scripts and programs that do not leverage the common structure of sequence elements present in genomics libraries.
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Booeshaghi et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68e71baab6db643587695902 — DOI: https://doi.org/10.1093/bioinformatics/btae168
A. Sina Booeshaghi
Xi Chen
Lior Pachter
Bioinformatics
University of California, Berkeley
California Institute of Technology
Southern University of Science and Technology
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